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You searched for subject:(Sickle cell disease). Showing records 1 – 30 of 187 total matches.

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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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


Universidade Estadual de Campinas

2. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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 Southern California

3. Gonsalves, Caryn Suzanne. A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease.

Degree: PhD, Biochemistry & Molecular Biology, 2009, University of Southern California

 In sickle cell disease (SCD), low oxygen tension results in sickle cell hemoglobin polymerization, causing the sickling of red blood cells, with subsequent vaso-occlusions (137).… (more)

Subjects/Keywords: leukotrienes; sickle cell disease

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APA (6th Edition):

Gonsalves, C. S. (2009). A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/252837/rec/288

Chicago Manual of Style (16th Edition):

Gonsalves, Caryn Suzanne. “A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease.” 2009. Doctoral Dissertation, University of Southern California. Accessed October 22, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/252837/rec/288.

MLA Handbook (7th Edition):

Gonsalves, Caryn Suzanne. “A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease.” 2009. Web. 22 Oct 2019.

Vancouver:

Gonsalves CS. A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Oct 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/252837/rec/288.

Council of Science Editors:

Gonsalves CS. A novel role for hypoxia-inducible factor-1alpha (HIF-1alpha) in the regulation of inflammatory chemokines and leukotriene expression in sickle cell disease. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/252837/rec/288


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)

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Wilson WE. The Psychosocial Impact of Sickle Cell Disease (SCD) on Partners of SCD Patients . [Internet] [Masters thesis]. University of Ghana; 2018. [cited 2019 Oct 22]. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Osbourne C. Sickle cell disease awareness amongst college students. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Oct 22]. 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

6. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


Case Western Reserve University

7. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


Georgia State University

8. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Martin SR. Peer Support in Adolescents Hospitalized for Sickle Cell Pain Crises. [Internet] [Doctoral dissertation]. Georgia State University; 2015. [cited 2019 Oct 22]. 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 Tech

9. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


Boston University

10. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Kittredge J. A retrospective assessment of routine renal function screening in patients with sickle cell disease. [Internet] [Masters thesis]. Boston University; 2014. [cited 2019 Oct 22]. 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


Georgia Tech

11. Selma, Jada M. The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2019, Georgia Tech

Sickle cell disease (SCD) is the most common inherited blood disorder in the United States. SCD affects approximately 100,000 people domestically and an additional 300,000… (more)

Subjects/Keywords: Sickle cell disease; Sphingolipids; Bone loss

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APA (6th Edition):

Selma, J. M. (2019). The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61242

Chicago Manual of Style (16th Edition):

Selma, Jada M. “The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells.” 2019. Doctoral Dissertation, Georgia Tech. Accessed October 22, 2019. http://hdl.handle.net/1853/61242.

MLA Handbook (7th Edition):

Selma, Jada M. “The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells.” 2019. Web. 22 Oct 2019.

Vancouver:

Selma JM. The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1853/61242.

Council of Science Editors:

Selma JM. The Role of Sphingolipid Metabolism in Sickle Bone Disease and Bone Stem Cells. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61242


University of Bridgeport

12. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Holloway R. The Efficacy of Butyric Acid in Ameliorating Clinical Symptoms of Sickle Cell Disease . [Internet] [Thesis]. University of Bridgeport; 2013. [cited 2019 Oct 22]. 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 Ghana

13. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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 Bath

14. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Al-Kitani M. Physiological responses to exercise in Omani children with sickle cell disease. [Internet] [Doctoral dissertation]. University of Bath; 2013. [cited 2019 Oct 22]. 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 Texas – Austin

15. -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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


University of Florida

16. Bermudez, Dayana. Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti.

Degree: 2011, University of Florida

 There is limited information on socio-behavioral factors influencing the perceptions and knowledge about sickle cell anemia (SCA) and malaria at the individual and community level… (more)

Subjects/Keywords: Blood; Diseases; Hemoglobins; Infections; Malaria; Questionnaires; Sickle cell anemia; Sickle cell disease; Sickles; Socioeconomic status; Haiti; Malaria; Sickle cell anemia

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APA (6th Edition):

Bermudez, D. (2011). Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060388

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):

Bermudez, Dayana. “Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti.” 2011. Thesis, University of Florida. Accessed October 22, 2019. http://ufdc.ufl.edu/AA00060388.

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

MLA Handbook (7th Edition):

Bermudez, Dayana. “Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti.” 2011. Web. 22 Oct 2019.

Vancouver:

Bermudez D. Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti. [Internet] [Thesis]. University of Florida; 2011. [cited 2019 Oct 22]. Available from: http://ufdc.ufl.edu/AA00060388.

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

Council of Science Editors:

Bermudez D. Socio-Behavioral Perceptions of Sickle Cell Anemia and Malaria in Haiti. [Thesis]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/AA00060388

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


Northeastern University

17. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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

18. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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

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

Degree: 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

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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. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/1798

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):

Exum, Kayzandra L. “The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease.” 2013. Thesis, East Carolina University. Accessed October 22, 2019. http://hdl.handle.net/10342/1798.

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

MLA Handbook (7th Edition):

Exum, Kayzandra L. “The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease.” 2013. Web. 22 Oct 2019.

Vancouver:

Exum KL. The Effects of Family Functioning on Academic Achievement in Children with Sickle Cell Disease. [Internet] [Thesis]. East Carolina University; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10342/1798.

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

Council of Science Editors:

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

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

20. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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

21. 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;

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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

22. Karen Simone Romanello. Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme.

Degree: 2013, Universidade Federal de São Carlos

Reactive Oxygen Species (ROS) are generated by the incomplete reduction of oxygen during metabolic processes, exposure to external agents and as a secondary response to… (more)

Subjects/Keywords: Peroxirredoxinas; Genética; Anemia falciforme; Peroxiredoxins; Sickle cell disease; Thalassemia; Talassemia; GENETICA

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APA (6th Edition):

Romanello, K. S. (2013). Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme. (Thesis). Universidade Federal de São Carlos. Retrieved from http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=6883

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):

Romanello, Karen Simone. “Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme.” 2013. Thesis, Universidade Federal de São Carlos. Accessed October 22, 2019. http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=6883.

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

MLA Handbook (7th Edition):

Romanello, Karen Simone. “Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme.” 2013. Web. 22 Oct 2019.

Vancouver:

Romanello KS. Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme. [Internet] [Thesis]. Universidade Federal de São Carlos; 2013. [cited 2019 Oct 22]. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=6883.

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

Council of Science Editors:

Romanello KS. Análise da expressão gênica das peroxirredoxinas em pacientes talassêmicos e com anemia falciforme. [Thesis]. Universidade Federal de São Carlos; 2013. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=6883

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


University of Cincinnati

23. Barber, Latorya Arnold. The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells.

Degree: PhD, Medicine : Pathobiology and Molecular Medicine, 2009, University of Cincinnati

  Phosphatidylserine (PS) externalization occurs in sickle red blood cells (RBC) and is thought to contribute to (1) increased sickle RBC-endothelial cell adhesion, (2) increased… (more)

Subjects/Keywords: Molecular Biology; Sickle Cell Disease; Red Blood Cells; Phosphatidylserine

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APA (6th Edition):

Barber, L. A. (2009). The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243353188

Chicago Manual of Style (16th Edition):

Barber, Latorya Arnold. “The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243353188.

MLA Handbook (7th Edition):

Barber, Latorya Arnold. “The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells.” 2009. Web. 22 Oct 2019.

Vancouver:

Barber LA. The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243353188.

Council of Science Editors:

Barber LA. The Activity of Lipid Transport Proteins in Normal and Sickle Red Blood Cells. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243353188

24. Darcielle Bruna Dias Elias. AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia.

Degree: Master, 2009, Universidade Federal do Ceará

 A anemia falciforme (AF) se caracteriza por anemia hemolÃtica crÃnica e com fenÃmenos vaso-oclusivos, seguidos de lesÃes a ÃrgÃos alvos, responsÃveis pela mortalidade associada a… (more)

Subjects/Keywords: FARMACIA; Anemia Falciforme; MalonaldeÃdo; HidroxiurÃia; Sickle-Cell Disease; Malonaldehyde; Hydroxyurea

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APA (6th Edition):

Elias, D. B. D. (2009). AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=3798 ;

Chicago Manual of Style (16th Edition):

Elias, Darcielle Bruna Dias. “AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia.” 2009. Masters Thesis, Universidade Federal do Ceará. Accessed October 22, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=3798 ;.

MLA Handbook (7th Edition):

Elias, Darcielle Bruna Dias. “AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia.” 2009. Web. 22 Oct 2019.

Vancouver:

Elias DBD. AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia. [Internet] [Masters thesis]. Universidade Federal do Ceará 2009. [cited 2019 Oct 22]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=3798 ;.

Council of Science Editors:

Elias DBD. AvaliaÃÃo dos NÃveis SÃricos de MalonaldeÃdo (MDA), Ãxido NÃtrico (NO) e Lactato Desidrogenase LÃctica (LDH) na Anemia Falciforme e suas CorrelaÃÃes Com o uso de HidroxiurÃia. [Masters Thesis]. Universidade Federal do Ceará 2009. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=3798 ;


Georgia Tech

25. Keegan, Philip Michael. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.

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

Sickle cell disease is a genetic disorder that affects 100,000 Americans and millions more worldwide. Although the sickle mutation affects one protein, which is only… (more)

Subjects/Keywords: Sickle cell disease; Arterial remodeling; Cathepsins; Stroke; Hemodynamics; Shear stress

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APA (6th Edition):

Keegan, P. M. (2014). Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54289

Chicago Manual of Style (16th Edition):

Keegan, Philip Michael. “Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.” 2014. Doctoral Dissertation, Georgia Tech. Accessed October 22, 2019. http://hdl.handle.net/1853/54289.

MLA Handbook (7th Edition):

Keegan, Philip Michael. “Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.” 2014. Web. 22 Oct 2019.

Vancouver:

Keegan PM. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1853/54289.

Council of Science Editors:

Keegan PM. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54289

26. Clayton-Jones, Dora L. Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study.

Degree: 2014, Marquette University

Sickle cell disease (SCD) is a serious debilitating chronic illness and global health problem. Spirituality and religiosity have been shown to have positive correlations with… (more)

Subjects/Keywords: adolescents, pediatric, religiosity, sickle cell disease, spirituality; Nursing

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APA (6th Edition):

Clayton-Jones, D. L. (2014). Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/341

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):

Clayton-Jones, Dora L. “Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study.” 2014. Thesis, Marquette University. Accessed October 22, 2019. https://epublications.marquette.edu/dissertations_mu/341.

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

MLA Handbook (7th Edition):

Clayton-Jones, Dora L. “Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study.” 2014. Web. 22 Oct 2019.

Vancouver:

Clayton-Jones DL. Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study. [Internet] [Thesis]. Marquette University; 2014. [cited 2019 Oct 22]. Available from: https://epublications.marquette.edu/dissertations_mu/341.

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

Council of Science Editors:

Clayton-Jones DL. Spirituality And Religiosity In Adolescents With Sickle Cell Disease: A Descriptive Qualitative Study. [Thesis]. Marquette University; 2014. Available from: https://epublications.marquette.edu/dissertations_mu/341

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


Kent State University

27. 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

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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 October 22, 2019. 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. 22 Oct 2019.

Vancouver:

Wilson SM. Relationship between Executive Functioning and Adherence in Youth with Sickle Cell Disease. [Internet] [Doctoral dissertation]. Kent State University; 2016. [cited 2019 Oct 22]. 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

28. 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

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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 October 22, 2019. 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. 22 Oct 2019.

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 2019 Oct 22]. 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


University of Southern California

29. Taskar, Pranali. Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1.

Degree: MS, Molecular Microbiology and Immunology, 2013, University of Southern California

 Hemeoxygenase-1 (HO-1) is a detoxifying enzyme produced by cells in response to oxidative stress. It is up-regulated in Sickle Cell Disease patients due to RBC… (more)

Subjects/Keywords: PlGF; hemeoxygenase-1; miRNA; sickle cell disease; hypoxia; HIF-1

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

APA (6th Edition):

Taskar, P. (2013). Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249995/rec/5063

Chicago Manual of Style (16th Edition):

Taskar, Pranali. “Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1.” 2013. Masters Thesis, University of Southern California. Accessed October 22, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249995/rec/5063.

MLA Handbook (7th Edition):

Taskar, Pranali. “Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1.” 2013. Web. 22 Oct 2019.

Vancouver:

Taskar P. Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2019 Oct 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249995/rec/5063.

Council of Science Editors:

Taskar P. Placental growth factor mediated transcriptional and post-transcriptional regulation of hemeoxygenase-1. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249995/rec/5063


University of Illinois – Chicago

30. Saraf, Santosh. Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia.

Degree: 2014, University of Illinois – Chicago

 To evaluate the association between hemoglobinuria and chronic kidney disease (CKD) in sickle cell anemia (SCA), we analyzed 356 adult hemoglobin SS or Sβo thalassemia… (more)

Subjects/Keywords: 1) Sickle Cell; 2) Chronic Kidney Disease; 3) Hemoglobinuria

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

APA (6th Edition):

Saraf, S. (2014). Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18907

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):

Saraf, Santosh. “Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia.” 2014. Thesis, University of Illinois – Chicago. Accessed October 22, 2019. http://hdl.handle.net/10027/18907.

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

MLA Handbook (7th Edition):

Saraf, Santosh. “Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia.” 2014. Web. 22 Oct 2019.

Vancouver:

Saraf S. Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10027/18907.

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

Council of Science Editors:

Saraf S. Hemolysis & Hemoglobinuria Are Associated With Chronic Kidney Disease In Patients With Sickle Cell Anemia. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18907

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

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