Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Sickle cell Disease). Showing records 1 – 30 of 230 total matches.

[1] [2] [3] [4] [5] [6] [7] [8]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Zambia

1. Wasomwe, Mercy Mumba. Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia .

Degree: 2012, University of Zambia

Sickle Cell Disease (SCD) is a chronic incurable genetic blood disorder that affects the Haemoglobin (Hb) within the Red Blood Cell (RBC).The disease affects millions… (more)

Subjects/Keywords: Sickle Cell Disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wasomwe, M. M. (2012). Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia . (Thesis). University of Zambia. Retrieved from http://hdl.handle.net/123456789/1463

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wasomwe, Mercy Mumba. “Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia .” 2012. Thesis, University of Zambia. Accessed September 23, 2020. http://hdl.handle.net/123456789/1463.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wasomwe, Mercy Mumba. “Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia .” 2012. Web. 23 Sep 2020.

Vancouver:

Wasomwe MM. Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia . [Internet] [Thesis]. University of Zambia; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/123456789/1463.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wasomwe MM. Problems encountered by immediate families in caring for children affected with sickle cell disease.University Teaching Hospital,Lusaka, Zambia . [Thesis]. University of Zambia; 2012. Available from: http://hdl.handle.net/123456789/1463

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Larissi, Aikaterini. Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο.

Degree: 2019, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

The phenotypic diversity of the disease presents a remarkable degree of clinical heterogeneity as the frequency of clinical complications varies significantly either with the person… (more)

Subjects/Keywords: Δρεπανοκυτταρική νόσος; Sickle Cell Disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Larissi, A. (2019). Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/45899

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Larissi, Aikaterini. “Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο.” 2019. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed September 23, 2020. http://hdl.handle.net/10442/hedi/45899.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Larissi, Aikaterini. “Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο.” 2019. Web. 23 Sep 2020.

Vancouver:

Larissi A. Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2019. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10442/hedi/45899.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Larissi A. Αλληλεπιδράσεις ενδοθηλιακής διαταραχής, φλεγμονής και αγγειογένεσης σε ασθενείς με δρεπανοκυτταρική νόσο. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2019. Available from: http://hdl.handle.net/10442/hedi/45899

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

3. Camila Bononi de Almeida. Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal.

Degree: Faculdade de Ciências Médicas, 2006, Universidade Estadual de Campinas

Sickle cell disease (SCD) is a systemic disease with a multifaceted pathophysiology; the polymerisation of the sickle haemoglobin molecule (HbS), when deoxygenated, has many consequences… (more)

Subjects/Keywords: Anemia falciforme; Sickle cell disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Almeida, C. B. d. (2006). Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal. (Thesis). Universidade Estadual de Campinas. Retrieved from http://libdigi.unicamp.br/document/?code=vtls000415329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Almeida, Camila Bononi de. “Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal.” 2006. Thesis, Universidade Estadual de Campinas. Accessed September 23, 2020. http://libdigi.unicamp.br/document/?code=vtls000415329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Almeida, Camila Bononi de. “Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal.” 2006. Web. 23 Sep 2020.

Vancouver:

Almeida CBd. Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal. [Internet] [Thesis]. Universidade Estadual de Campinas; 2006. [cited 2020 Sep 23]. Available from: http://libdigi.unicamp.br/document/?code=vtls000415329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Almeida CBd. Caracterização das fosfodiesterases (PDE) de GMPc nas celulas de linhagem eritroide e efeitos de drogas inibidoras de PDE na produção de hemoglobina fetal. [Thesis]. Universidade Estadual de Campinas; 2006. Available from: http://libdigi.unicamp.br/document/?code=vtls000415329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Ghana

4. Wilson, W.E. The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients .

Degree: 2018, University of Ghana

 The purpose of this study was to investigate the psychosocial effects that partners of SCD patients experience as a result of their relationship with the… (more)

Subjects/Keywords: Psychosocial; Sickle Cell Disease (SCD)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wilson, W. E. (2018). The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/28365

Chicago Manual of Style (16th Edition):

Wilson, W E. “The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients .” 2018. Masters Thesis, University of Ghana. Accessed September 23, 2020. http://ugspace.ug.edu.gh/handle/123456789/28365.

MLA Handbook (7th Edition):

Wilson, W E. “The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients .” 2018. Web. 23 Sep 2020.

Vancouver:

Wilson WE. The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients . [Internet] [Masters thesis]. University of Ghana; 2018. [cited 2020 Sep 23]. Available from: http://ugspace.ug.edu.gh/handle/123456789/28365.

Council of Science Editors:

Wilson WE. The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients . [Masters Thesis]. University of Ghana; 2018. Available from: http://ugspace.ug.edu.gh/handle/123456789/28365


University of Illinois – Urbana-Champaign

5. Osbourne, Cassie. Sickle cell disease awareness amongst college students.

Degree: M.S.P.H., 0349, 2012, University of Illinois – Urbana-Champaign

 This descriptive study was designed to investigate if college students attending a midwestern university are aware of the clinical manifestations, treatments, and genetic counseling methods… (more)

Subjects/Keywords: sickle cell disease; college students

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Osbourne, C. (2012). Sickle cell disease awareness amongst college students. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29465

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Osbourne, Cassie. “Sickle cell disease awareness amongst college students.” 2012. Thesis, University of Illinois – Urbana-Champaign. Accessed September 23, 2020. http://hdl.handle.net/2142/29465.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Osbourne, Cassie. “Sickle cell disease awareness amongst college students.” 2012. Web. 23 Sep 2020.

Vancouver:

Osbourne C. Sickle cell disease awareness amongst college students. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2142/29465.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Osbourne C. Sickle cell disease awareness amongst college students. [Thesis]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29465

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Case Western Reserve University

6. Moxley, Kristan Michelle. Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia.

Degree: MSs, Genetic Counseling Training Program, 2008, Case Western Reserve University

 This descriptive study assessed 154 pregnant African American women’s knowledge of and 11 health care providers’ protocols for sickle cell disease carrier screening. The patient… (more)

Subjects/Keywords: Knowledge of sickle cell trait; Knowledge of sickle cell disease; Knowledge of sickle cell anemia; African American knowledge of sickle cell

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Moxley, K. M. (2008). Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1201280917

Chicago Manual of Style (16th Edition):

Moxley, Kristan Michelle. “Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia.” 2008. Masters Thesis, Case Western Reserve University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1201280917.

MLA Handbook (7th Edition):

Moxley, Kristan Michelle. “Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia.” 2008. Web. 23 Sep 2020.

Vancouver:

Moxley KM. Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia. [Internet] [Masters thesis]. Case Western Reserve University; 2008. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1201280917.

Council of Science Editors:

Moxley KM. Impact of Carrier Screening on Pregnant Women’s Knowledge of Sickle Cell Anemia. [Masters Thesis]. Case Western Reserve University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1201280917


University of Ghana

7. Boadu, L.O. Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region .

Degree: 2017, University of Ghana

 Introduction: Sickle Cell Disease (SCD) is progressively gaining the recognition that was once ignored despite its increasingly higher prevalence of 2-3 % in the World… (more)

Subjects/Keywords: Sickle Cell Disease; Ghana; Sickle Cell Clinic; SCC; SCD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Boadu, L. O. (2017). Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/35595

Chicago Manual of Style (16th Edition):

Boadu, L O. “Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region .” 2017. Masters Thesis, University of Ghana. Accessed September 23, 2020. http://ugspace.ug.edu.gh/handle/123456789/35595.

MLA Handbook (7th Edition):

Boadu, L O. “Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region .” 2017. Web. 23 Sep 2020.

Vancouver:

Boadu LO. Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region . [Internet] [Masters thesis]. University of Ghana; 2017. [cited 2020 Sep 23]. Available from: http://ugspace.ug.edu.gh/handle/123456789/35595.

Council of Science Editors:

Boadu LO. Household Cost of Sickle Cell Disease Among Patients of Sickle Cell Clinic. Tema General Hospital, Greater Accra Region . [Masters Thesis]. University of Ghana; 2017. Available from: http://ugspace.ug.edu.gh/handle/123456789/35595


Boston University

8. Kittredge, Justin. A retrospective assessment of routine renal function screening in patients with sickle cell disease.

Degree: MS, Medical Sciences, 2014, Boston University

 BACKGROUND Routine renal screens are essential to the healthcare maintenance of pediatric patients with sickle cell disease. There is an inadequate amount of evidence, however,… (more)

Subjects/Keywords: Medicine; Cell; Disease; Function; Renal; Screen; Sickle

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kittredge, J. (2014). A retrospective assessment of routine renal function screening in patients with sickle cell disease. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/15327

Chicago Manual of Style (16th Edition):

Kittredge, Justin. “A retrospective assessment of routine renal function screening in patients with sickle cell disease.” 2014. Masters Thesis, Boston University. Accessed September 23, 2020. http://hdl.handle.net/2144/15327.

MLA Handbook (7th Edition):

Kittredge, Justin. “A retrospective assessment of routine renal function screening in patients with sickle cell disease.” 2014. Web. 23 Sep 2020.

Vancouver:

Kittredge J. A retrospective assessment of routine renal function screening in patients with sickle cell disease. [Internet] [Masters thesis]. Boston University; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2144/15327.

Council of Science Editors:

Kittredge J. A retrospective assessment of routine renal function screening in patients with sickle cell disease. [Masters Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15327

9. Josset, Éliane. Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers.

Degree: Docteur es, Psychologie, 2017, Sorbonne Paris Cité

La drépanocytose est la maladie génétique la plus fréquente au monde. Elle se manifeste principalement par une douleur intense et imprévisible. Les crises de douleur… (more)

Subjects/Keywords: Drépanocytose; Représentations; Sickle cell disease; Representation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Josset, . (2017). Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC330

Chicago Manual of Style (16th Edition):

Josset, Éliane. “Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed September 23, 2020. http://www.theses.fr/2017USPCC330.

MLA Handbook (7th Edition):

Josset, Éliane. “Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers.” 2017. Web. 23 Sep 2020.

Vancouver:

Josset . Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Sep 23]. Available from: http://www.theses.fr/2017USPCC330.

Council of Science Editors:

Josset . Le corps de l’enfant à l'épreuve de la drépanocytose : traitement psychique de la douleur et représentations de la maladie dans les dessins d’enfants et le discours des patients, des familles et des soignants : The body of children proof against sickle cell disease : psychic treatment of pain and representation of the disease in children’s drawings and discourse of patients, families and caregivers. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC330


University of Ghana

10. Anaman, S. Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital .

Degree: 2018, University of Ghana

Sickle Cell Disease is the most common life-threatening hematologic disorder found in Ghanaian children. The present system of care of these children relies mostly on… (more)

Subjects/Keywords: Sickle Cell Disease; 37 Military Hospital

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Anaman, S. (2018). Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/30022

Chicago Manual of Style (16th Edition):

Anaman, S. “Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital .” 2018. Masters Thesis, University of Ghana. Accessed September 23, 2020. http://ugspace.ug.edu.gh/handle/123456789/30022.

MLA Handbook (7th Edition):

Anaman, S. “Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital .” 2018. Web. 23 Sep 2020.

Vancouver:

Anaman S. Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital . [Internet] [Masters thesis]. University of Ghana; 2018. [cited 2020 Sep 23]. Available from: http://ugspace.ug.edu.gh/handle/123456789/30022.

Council of Science Editors:

Anaman S. Experiences of Parents of Children with Sickle Cell Disease: A Study at 37 Military Hospital . [Masters Thesis]. University of Ghana; 2018. Available from: http://ugspace.ug.edu.gh/handle/123456789/30022


University of Bridgeport

11. Holloway, Ronelle. The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease .

Degree: 2013, University of Bridgeport

 Statistics from the CDC and NIH indicate that 70,000 to 80,000 people in the United States have SCD. The disease is estimated to occur in… (more)

Subjects/Keywords: Naturopathy; Butyric acid; Sickle cell disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Holloway, R. (2013). The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease . (Thesis). University of Bridgeport. Retrieved from https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1402

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Holloway, Ronelle. “The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease .” 2013. Thesis, University of Bridgeport. Accessed September 23, 2020. https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1402.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Holloway, Ronelle. “The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease .” 2013. Web. 23 Sep 2020.

Vancouver:

Holloway R. The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease . [Internet] [Thesis]. University of Bridgeport; 2013. [cited 2020 Sep 23]. Available from: https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1402.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Holloway R. The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease . [Thesis]. University of Bridgeport; 2013. Available from: https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1402

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Bath

12. Al-Kitani, Mahfoodha. Physiological responses to exercise in Omani children with sickle cell disease.

Degree: PhD, 2013, University of Bath

 According to the national survey of genetic blood disorders, the prevalence of haemoglobinopathies in Oman is 9.5% with Sickle Cell Disease (SCD) and Sickle Cell(more)

Subjects/Keywords: 616.1; sickle cell disease; children; exercise

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Al-Kitani, M. (2013). Physiological responses to exercise in Omani children with sickle cell disease. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/physiological-responses-to-exercise-in-omani-children-with-sickle-cell-disease(fe834a03-4ef6-4dc5-8e3b-f299c986b4ba).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.577754

Chicago Manual of Style (16th Edition):

Al-Kitani, Mahfoodha. “Physiological responses to exercise in Omani children with sickle cell disease.” 2013. Doctoral Dissertation, University of Bath. Accessed September 23, 2020. https://researchportal.bath.ac.uk/en/studentthesis/physiological-responses-to-exercise-in-omani-children-with-sickle-cell-disease(fe834a03-4ef6-4dc5-8e3b-f299c986b4ba).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.577754.

MLA Handbook (7th Edition):

Al-Kitani, Mahfoodha. “Physiological responses to exercise in Omani children with sickle cell disease.” 2013. Web. 23 Sep 2020.

Vancouver:

Al-Kitani M. Physiological responses to exercise in Omani children with sickle cell disease. [Internet] [Doctoral dissertation]. University of Bath; 2013. [cited 2020 Sep 23]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/physiological-responses-to-exercise-in-omani-children-with-sickle-cell-disease(fe834a03-4ef6-4dc5-8e3b-f299c986b4ba).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.577754.

Council of Science Editors:

Al-Kitani M. Physiological responses to exercise in Omani children with sickle cell disease. [Doctoral Dissertation]. University of Bath; 2013. Available from: https://researchportal.bath.ac.uk/en/studentthesis/physiological-responses-to-exercise-in-omani-children-with-sickle-cell-disease(fe834a03-4ef6-4dc5-8e3b-f299c986b4ba).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.577754


University of Ghana

13. Wilson, A.A. Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children .

Degree: 2019, University of Ghana

 Background: The opening of a Bone Marrow Transplant centre at the Greater Accra Regional hospital, the first centre in Ghana, provides an opportunity for caregivers… (more)

Subjects/Keywords: Bone Marrow Transplant; Sickle Cell Disease; Children

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wilson, A. A. (2019). Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/33043

Chicago Manual of Style (16th Edition):

Wilson, A A. “Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children .” 2019. Masters Thesis, University of Ghana. Accessed September 23, 2020. http://ugspace.ug.edu.gh/handle/123456789/33043.

MLA Handbook (7th Edition):

Wilson, A A. “Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children .” 2019. Web. 23 Sep 2020.

Vancouver:

Wilson AA. Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children . [Internet] [Masters thesis]. University of Ghana; 2019. [cited 2020 Sep 23]. Available from: http://ugspace.ug.edu.gh/handle/123456789/33043.

Council of Science Editors:

Wilson AA. Caregivers’ Willingness to Pay for Bone Marrow Transplant to Cure Sickle Cell Disease in Children . [Masters Thesis]. University of Ghana; 2019. Available from: http://ugspace.ug.edu.gh/handle/123456789/33043


University of Texas – Austin

14. -7134-077X. Health literacy in adolescents with Sickle Cell Disease.

Degree: PhD, Nursing, 2015, University of Texas – Austin

 Health literacy is "the degree to which individuals have the capacity to obtain, process, and understand basic health information and services needed to make appropriate… (more)

Subjects/Keywords: Health literacy; Adolescents; Sickle Cell Disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

-7134-077X. (2015). Health literacy in adolescents with Sickle Cell Disease. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31599

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7134-077X. “Health literacy in adolescents with Sickle Cell Disease.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 23, 2020. http://hdl.handle.net/2152/31599.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-7134-077X. “Health literacy in adolescents with Sickle Cell Disease.” 2015. Web. 23 Sep 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-7134-077X. Health literacy in adolescents with Sickle Cell Disease. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2152/31599.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-7134-077X. Health literacy in adolescents with Sickle Cell Disease. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/31599

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Georgia State University

15. Martin, Sarah R. Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises.

Degree: PhD, Psychology, 2015, Georgia State University

Sickle cell disease (SCD) is an inherited blood disorder, which has a range of symptoms including pain, fatigue, organ damage, and immunodeficiency. Patients are… (more)

Subjects/Keywords: Adolescents; Pain; Sickle Cell Disease; Social Support

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Martin, S. R. (2015). Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/psych_diss/142

Chicago Manual of Style (16th Edition):

Martin, Sarah R. “Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises.” 2015. Doctoral Dissertation, Georgia State University. Accessed September 23, 2020. https://scholarworks.gsu.edu/psych_diss/142.

MLA Handbook (7th Edition):

Martin, Sarah R. “Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises.” 2015. Web. 23 Sep 2020.

Vancouver:

Martin SR. Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises. [Internet] [Doctoral dissertation]. Georgia State University; 2015. [cited 2020 Sep 23]. Available from: https://scholarworks.gsu.edu/psych_diss/142.

Council of Science Editors:

Martin SR. Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises. [Doctoral Dissertation]. Georgia State University; 2015. Available from: https://scholarworks.gsu.edu/psych_diss/142


Georgia State University

16. Cousins, Laura Ann. Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease.

Degree: PhD, Psychology, 2017, Georgia State University

  Living with sickle cell disease (SCD) can be a significant adversity due to disease-related symptoms and complications. Compounding these challenges, SCD predominantly affects ethnic… (more)

Subjects/Keywords: Resilience; Adolescents; Sickle cell disease; Pain management

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cousins, L. A. (2017). Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/psych_diss/171

Chicago Manual of Style (16th Edition):

Cousins, Laura Ann. “Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease.” 2017. Doctoral Dissertation, Georgia State University. Accessed September 23, 2020. https://scholarworks.gsu.edu/psych_diss/171.

MLA Handbook (7th Edition):

Cousins, Laura Ann. “Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease.” 2017. Web. 23 Sep 2020.

Vancouver:

Cousins LA. Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease. [Internet] [Doctoral dissertation]. Georgia State University; 2017. [cited 2020 Sep 23]. Available from: https://scholarworks.gsu.edu/psych_diss/171.

Council of Science Editors:

Cousins LA. Exploring Resilience and Adaptation in Adolescents with Sickle Cell Disease. [Doctoral Dissertation]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/psych_diss/171


Georgia Tech

17. Awojoodu, Anthony O. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

Sickle cell disease is a hereditary blood disorder caused by a point mutation in the gene encoding hemoglobin. This mutation causes hemoglobin molecules to polymerize… (more)

Subjects/Keywords: Sickle cell disease; Inflammation; Sphingolipid; Microparticles

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Awojoodu, A. O. (2014). Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54286

Chicago Manual of Style (16th Edition):

Awojoodu, Anthony O. “Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.” 2014. Doctoral Dissertation, Georgia Tech. Accessed September 23, 2020. http://hdl.handle.net/1853/54286.

MLA Handbook (7th Edition):

Awojoodu, Anthony O. “Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.” 2014. Web. 23 Sep 2020.

Vancouver:

Awojoodu AO. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1853/54286.

Council of Science Editors:

Awojoodu AO. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54286


East Carolina University

18. Alston, Kristen Janay. Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors.

Degree: PhD, Psychology: Clinical Psychology, 2015, East Carolina University

 The present study sought to ascertain whether treatment adherence in a pediatric SCD population is best described as a multidimensional or global construct by 1)… (more)

Subjects/Keywords: Clinical psychology; Pediatric; Sickle cell disease; Treatment adherence; Patient compliance; Sickle cell anemia in children; Sickle cell anemia in adolescence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Alston, K. J. (2015). Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/4983

Chicago Manual of Style (16th Edition):

Alston, Kristen Janay. “Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors.” 2015. Doctoral Dissertation, East Carolina University. Accessed September 23, 2020. http://hdl.handle.net/10342/4983.

MLA Handbook (7th Edition):

Alston, Kristen Janay. “Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors.” 2015. Web. 23 Sep 2020.

Vancouver:

Alston KJ. Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors. [Internet] [Doctoral dissertation]. East Carolina University; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10342/4983.

Council of Science Editors:

Alston KJ. Treatment Adherence In Pediatric Sickle Cell Disease : Examining Medication Adherence, Appointment Keeping, And Self-Care Behaviors. [Doctoral Dissertation]. East Carolina University; 2015. Available from: http://hdl.handle.net/10342/4983


Northeastern University

19. Abimbola, Olatundun. Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia.

Degree: EdD, School of Education, 2016, Northeastern University

 This qualitative research is the first of its kind to proffer a comprehensive look into the educational experiences of individuals living with Sickle Cell Anemia… (more)

Subjects/Keywords: higher education; pain crisis; resilience; sickle cell anemia; sickle cell disease; stress

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abimbola, O. (2016). Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20248548

Chicago Manual of Style (16th Edition):

Abimbola, Olatundun. “Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia.” 2016. Doctoral Dissertation, Northeastern University. Accessed September 23, 2020. http://hdl.handle.net/2047/D20248548.

MLA Handbook (7th Edition):

Abimbola, Olatundun. “Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia.” 2016. Web. 23 Sep 2020.

Vancouver:

Abimbola O. Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2047/D20248548.

Council of Science Editors:

Abimbola O. Education and sickle cell anemia: a narrative study of the educational experiences of individuals living with sickle cell anemia. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20248548


Florida Atlantic University

20. Dieujuste, Darryl. Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease.

Degree: MS, 2018, Florida Atlantic University

Sickle cell disease is an inherited blood cell disorder that affects about 100,000 people in the US and results in high cost of medical care… (more)

Subjects/Keywords: Sickle cell disease; Sickle cell anemia – Diagnosis; Flow cytometry – Diagnostic use; Mobile Applications

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Dieujuste, D. (2018). Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease. (Masters Thesis). Florida Atlantic University. Retrieved from http://fau.digital.flvc.org/islandora/object/fau:40919

Chicago Manual of Style (16th Edition):

Dieujuste, Darryl. “Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease.” 2018. Masters Thesis, Florida Atlantic University. Accessed September 23, 2020. http://fau.digital.flvc.org/islandora/object/fau:40919.

MLA Handbook (7th Edition):

Dieujuste, Darryl. “Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease.” 2018. Web. 23 Sep 2020.

Vancouver:

Dieujuste D. Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease. [Internet] [Masters thesis]. Florida Atlantic University; 2018. [cited 2020 Sep 23]. Available from: http://fau.digital.flvc.org/islandora/object/fau:40919.

Council of Science Editors:

Dieujuste D. Development of A Portable Impedance Based Flow Cytometer for Diagnosis of Sickle Cell Disease. [Masters Thesis]. Florida Atlantic University; 2018. Available from: http://fau.digital.flvc.org/islandora/object/fau:40919


East Carolina University

21. Exum, Kayzandra L. The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease.

Degree: MA, Psychology: School Psychology, 2013, East Carolina University

Sickle cell disease (SCD) is a complex group of genetic blood disorders that currently affects 90,000-100,000 Americans primarily of African descent. SCD leads to physiological… (more)

Subjects/Keywords: Psychology; Educational psychology; Health sciences; Adolescents; Children; Family functioning; Schools; Sickle cell disease; Sickle cell anemia – Psychological aspects; Sickle cell anemia in children; Sickle cell anemia in adolescence; Academic achievement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Exum, K. L. (2013). The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/1798

Chicago Manual of Style (16th Edition):

Exum, Kayzandra L. “The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease.” 2013. Masters Thesis, East Carolina University. Accessed September 23, 2020. http://hdl.handle.net/10342/1798.

MLA Handbook (7th Edition):

Exum, Kayzandra L. “The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease.” 2013. Web. 23 Sep 2020.

Vancouver:

Exum KL. The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease. [Internet] [Masters thesis]. East Carolina University; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10342/1798.

Council of Science Editors:

Exum KL. The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease. [Masters Thesis]. East Carolina University; 2013. Available from: http://hdl.handle.net/10342/1798

22. Almashjary, Majed. The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease.

Degree: 2020, The Catholic University of America

Sickle cell disease (SCD) is caused by polymerization of deoxy-hemoglobin-S (HbS) within the red blood cell (RBC). HbS polymerization is a concentration-dependent process. I hypothesized… (more)

Subjects/Keywords: Hematology; Iron Deficiency Anemia; Red Blood Cell; Sickle Cell Disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Almashjary, M. (2020). The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease. (Thesis). The Catholic University of America. Retrieved from http://hdl.handle.net/1961/cuislandora:214730

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Almashjary, Majed. “The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease.” 2020. Thesis, The Catholic University of America. Accessed September 23, 2020. http://hdl.handle.net/1961/cuislandora:214730.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Almashjary, Majed. “The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease.” 2020. Web. 23 Sep 2020.

Vancouver:

Almashjary M. The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease. [Internet] [Thesis]. The Catholic University of America; 2020. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1961/cuislandora:214730.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Almashjary M. The Impact of Dietary Iron Restriction on Sickling Kinetics and Hemolysis in A Transgenic Model of Sickle Cell Disease. [Thesis]. The Catholic University of America; 2020. Available from: http://hdl.handle.net/1961/cuislandora:214730

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Florida Atlantic University

23. Liu, Jia. ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION.

Degree: 2019, Florida Atlantic University

Electrical impedance of cells is a sensitive indicator of changes in cellular structure and biophysical characteristics. Integration of electrical impedance sensing in microfluidics can be… (more)

Subjects/Keywords: Microfluidics; Erythrocytes; Electric Impedance; Sickle cell disease; Malaria; Cell Adhesion

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Liu, J. (2019). ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION. (Thesis). Florida Atlantic University. Retrieved from http://fau.digital.flvc.org/islandora/object/fau:42187

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Liu, Jia. “ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION.” 2019. Thesis, Florida Atlantic University. Accessed September 23, 2020. http://fau.digital.flvc.org/islandora/object/fau:42187.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Liu, Jia. “ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION.” 2019. Web. 23 Sep 2020.

Vancouver:

Liu J. ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION. [Internet] [Thesis]. Florida Atlantic University; 2019. [cited 2020 Sep 23]. Available from: http://fau.digital.flvc.org/islandora/object/fau:42187.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Liu J. ELECTRICAL IMPEDANCE SENSING OF ERYTHROCYTES AND CYTOADHESION. [Thesis]. Florida Atlantic University; 2019. Available from: http://fau.digital.flvc.org/islandora/object/fau:42187

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kent State University

24. Wilson, Shana M. Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease.

Degree: PhD, College of Arts and Sciences / Department of Psychology, 2016, Kent State University

 Executive functioning (EF) refers to the high-level processes responsible for purposeful behavior and encompasses abilities such as inhibition, planning, organization, and cognitive flexibility. Deficits in… (more)

Subjects/Keywords: Psychology; executive functioning; adherence; responsibility; sickle cell disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wilson, S. M. (2016). Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1473596375016865

Chicago Manual of Style (16th Edition):

Wilson, Shana M. “Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease.” 2016. Doctoral Dissertation, Kent State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1473596375016865.

MLA Handbook (7th Edition):

Wilson, Shana M. “Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease.” 2016. Web. 23 Sep 2020.

Vancouver:

Wilson SM. Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease. [Internet] [Doctoral dissertation]. Kent State University; 2016. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1473596375016865.

Council of Science Editors:

Wilson SM. Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease. [Doctoral Dissertation]. Kent State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1473596375016865


UCLA

25. Jones, Jenna. Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease.

Degree: Health Services, 2014, UCLA

 Introduction: Due to advances in medical knowledge and technology, life expectancy has increased for many child-onset complex chronic conditions including sickle cell disease (SCD). As… (more)

Subjects/Keywords: Health care management; Emergency Care; Hospitalizations; Sickle Cell Disease; Utilization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jones, J. (2014). Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/94f618vq

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jones, Jenna. “Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease.” 2014. Thesis, UCLA. Accessed September 23, 2020. http://www.escholarship.org/uc/item/94f618vq.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jones, Jenna. “Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease.” 2014. Web. 23 Sep 2020.

Vancouver:

Jones J. Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/94f618vq.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jones J. Hospitalization patterns and emergency department use for youth and young adults growing older with sickle cell disease. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/94f618vq

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

26. Santos, Elen Gonçalves dos. Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme.

Degree: PhD, Tecnologia Nuclear - Materiais, 2014, University of São Paulo

Segundo estimativas da Organização Mundial de Saúde (OMS) no Brasil nascem 3.500 crianças com anemia falciforme a cada ano e 20% delas não conseguem atingir… (more)

Subjects/Keywords: anemia falciforme; diagnosis; diagnóstico; hemoglobin S; hemoglobina S; sickle cell disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Santos, E. G. d. (2014). Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85134/tde-23072015-140021/ ;

Chicago Manual of Style (16th Edition):

Santos, Elen Gonçalves dos. “Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme.” 2014. Doctoral Dissertation, University of São Paulo. Accessed September 23, 2020. http://www.teses.usp.br/teses/disponiveis/85/85134/tde-23072015-140021/ ;.

MLA Handbook (7th Edition):

Santos, Elen Gonçalves dos. “Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme.” 2014. Web. 23 Sep 2020.

Vancouver:

Santos EGd. Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Sep 23]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85134/tde-23072015-140021/ ;.

Council of Science Editors:

Santos EGd. Desenvolvimento de uma metodologia rápida e de baixo custo para diagnóstico da Anemia Falciforme. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/85/85134/tde-23072015-140021/ ;


Temple University

27. Iampietro, Mary Catherine. An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease.

Degree: PhD, 2014, Temple University

Psychology

It is now well established that children with sickle cell disease (SCD) demonstrate cognitive deficits even in the absence of clinical stroke, but studies… (more)

Subjects/Keywords: Psychology;

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Iampietro, M. C. (2014). An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,301993

Chicago Manual of Style (16th Edition):

Iampietro, Mary Catherine. “An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease.” 2014. Doctoral Dissertation, Temple University. Accessed September 23, 2020. http://digital.library.temple.edu/u?/p245801coll10,301993.

MLA Handbook (7th Edition):

Iampietro, Mary Catherine. “An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease.” 2014. Web. 23 Sep 2020.

Vancouver:

Iampietro MC. An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Sep 23]. Available from: http://digital.library.temple.edu/u?/p245801coll10,301993.

Council of Science Editors:

Iampietro MC. An Investigation of Episodic Memory Performance in Relation to Inflammation in Children with Sickle Cell Disease. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,301993

28. Ocansey, Prince. Priapism Among Male Adolescents with Sickle Cell Disease.

Degree: PhD, Nursing, 2018, University of San Diego

  The purpose of this qualitative phenomenological study was to describe the lived experience of priapism among male adolescents with sickle cell disease (SCD). A… (more)

Subjects/Keywords: Priapism; Sickle Cell Disease; Adolescents; Southern California; Nursing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ocansey, P. (2018). Priapism Among Male Adolescents with Sickle Cell Disease. (Doctoral Dissertation). University of San Diego. Retrieved from https://digital.sandiego.edu/dissertations/115

Chicago Manual of Style (16th Edition):

Ocansey, Prince. “Priapism Among Male Adolescents with Sickle Cell Disease.” 2018. Doctoral Dissertation, University of San Diego. Accessed September 23, 2020. https://digital.sandiego.edu/dissertations/115.

MLA Handbook (7th Edition):

Ocansey, Prince. “Priapism Among Male Adolescents with Sickle Cell Disease.” 2018. Web. 23 Sep 2020.

Vancouver:

Ocansey P. Priapism Among Male Adolescents with Sickle Cell Disease. [Internet] [Doctoral dissertation]. University of San Diego; 2018. [cited 2020 Sep 23]. Available from: https://digital.sandiego.edu/dissertations/115.

Council of Science Editors:

Ocansey P. Priapism Among Male Adolescents with Sickle Cell Disease. [Doctoral Dissertation]. University of San Diego; 2018. Available from: https://digital.sandiego.edu/dissertations/115


University of Michigan

29. Reeves, Sarah Erin Leasure. Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease.

Degree: PhD, Epidemiological Science, 2013, University of Michigan

 Children with sickle cell disease (SCD) are at an increased risk of stroke. Transcranial Doppler (TCD) screening assesses the risk of stroke in children with… (more)

Subjects/Keywords: Pediatric Stroke; Sickle Cell Disease; Public Health; Health Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Reeves, S. E. L. (2013). Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102487

Chicago Manual of Style (16th Edition):

Reeves, Sarah Erin Leasure. “Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease.” 2013. Doctoral Dissertation, University of Michigan. Accessed September 23, 2020. http://hdl.handle.net/2027.42/102487.

MLA Handbook (7th Edition):

Reeves, Sarah Erin Leasure. “Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease.” 2013. Web. 23 Sep 2020.

Vancouver:

Reeves SEL. Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2027.42/102487.

Council of Science Editors:

Reeves SEL. Opportunities to Improve Transcranial Doppler Screening Among Children With Sickle Cell Disease. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102487


Vanderbilt University

30. Yarboi, Janet M. The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease.

Degree: MS, Psychology, 2014, Vanderbilt University

Sickle cell disease is a chronic, life-threatening condition that affects more than one in every 400 African-American newborns. In addition to being at greater risk… (more)

Subjects/Keywords: social-environmental stress; cognitive function; parenting; sickle cell disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Yarboi, J. M. (2014). The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yarboi, Janet M. “The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease.” 2014. Thesis, Vanderbilt University. Accessed September 23, 2020. http://hdl.handle.net/1803/12153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yarboi, Janet M. “The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease.” 2014. Web. 23 Sep 2020.

Vancouver:

Yarboi JM. The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease. [Internet] [Thesis]. Vanderbilt University; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1803/12153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yarboi JM. The Association of Social-Environmental Factors with Cognitive Function in Children with Sickle Cell Disease. [Thesis]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3] [4] [5] [6] [7] [8]

.