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You searched for subject:(Congenital). Showing records 1 – 30 of 1100 total matches.

[1] [2] [3] [4] [5] … [37]

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University of Manchester

1. Buhamad, Zahrah. Cytomegalovirus Glycoprotein Types and Disease Causation.

Degree: 2018, University of Manchester

 Human Cytomegalovirus (HCMV) is the most common cause of viral congenital infection in the world. Around 5-10% of HCMV infected children are symptomatic at birth,… (more)

Subjects/Keywords: Cytomegalovirus; Glycoproteins; Congenital

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

APA (6th Edition):

Buhamad, Z. (2018). Cytomegalovirus Glycoprotein Types and Disease Causation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313589

Chicago Manual of Style (16th Edition):

Buhamad, Zahrah. “Cytomegalovirus Glycoprotein Types and Disease Causation.” 2018. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313589.

MLA Handbook (7th Edition):

Buhamad, Zahrah. “Cytomegalovirus Glycoprotein Types and Disease Causation.” 2018. Web. 19 Sep 2020.

Vancouver:

Buhamad Z. Cytomegalovirus Glycoprotein Types and Disease Causation. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313589.

Council of Science Editors:

Buhamad Z. Cytomegalovirus Glycoprotein Types and Disease Causation. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313589

2. Zukosky, Kristen. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.

Degree: PhD, Neuroscience, 2015, Brown University

 The aim of this thesis research is to identify and model neuromuscular diseases. I focused on two particular congenital neuromuscular diseases. Among the many genes… (more)

Subjects/Keywords: congenital muscular diseases

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APA (6th Edition):

Zukosky, K. (2015). Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419380/

Chicago Manual of Style (16th Edition):

Zukosky, Kristen. “Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.” 2015. Doctoral Dissertation, Brown University. Accessed September 19, 2020. https://repository.library.brown.edu/studio/item/bdr:419380/.

MLA Handbook (7th Edition):

Zukosky, Kristen. “Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.” 2015. Web. 19 Sep 2020.

Vancouver:

Zukosky K. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2020 Sep 19]. Available from: https://repository.library.brown.edu/studio/item/bdr:419380/.

Council of Science Editors:

Zukosky K. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419380/

3. Onduru, Gervas Onduru. Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District.

Degree: 2016, University of Zimbabwe

 Toxoplasmosis is a zoonotic disease caused by an intracellular obligate coccidian protozoan called Toxoplasma gondii. The parasite infects all warm blooded animals and usually develops… (more)

Subjects/Keywords: Congenital toxoplasmosis; Toxoplasmosis

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APA (6th Edition):

Onduru, G. O. (2016). Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District. (Thesis). University of Zimbabwe. Retrieved from http://dspace.unza.zm/handle/123456789/4887

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):

Onduru, Gervas Onduru. “Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District.” 2016. Thesis, University of Zimbabwe. Accessed September 19, 2020. http://dspace.unza.zm/handle/123456789/4887.

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

MLA Handbook (7th Edition):

Onduru, Gervas Onduru. “Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District.” 2016. Web. 19 Sep 2020.

Vancouver:

Onduru GO. Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District. [Internet] [Thesis]. University of Zimbabwe; 2016. [cited 2020 Sep 19]. Available from: http://dspace.unza.zm/handle/123456789/4887.

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

Council of Science Editors:

Onduru GO. Evaluation of the level of awareness of congenital toxoplasmosis and associated practices among pregnant women and health workers in Tanzania's Temeke District. [Thesis]. University of Zimbabwe; 2016. Available from: http://dspace.unza.zm/handle/123456789/4887

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


University of Illinois – Chicago

4. Blaisdell, Julie Anne. Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies.

Degree: 2018, University of Illinois – Chicago

 Background: Nitrate is a common water contaminant that has been associated with adverse birth outcomes, including certain birth defects, although evidence is limited. The purpose… (more)

Subjects/Keywords: nitrate; congenital anomalies

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APA (6th Edition):

Blaisdell, J. A. (2018). Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22951

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):

Blaisdell, Julie Anne. “Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies.” 2018. Thesis, University of Illinois – Chicago. Accessed September 19, 2020. http://hdl.handle.net/10027/22951.

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

MLA Handbook (7th Edition):

Blaisdell, Julie Anne. “Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies.” 2018. Web. 19 Sep 2020.

Vancouver:

Blaisdell JA. Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10027/22951.

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

Council of Science Editors:

Blaisdell JA. Maternal Exposure to Nitrate through Drinking Water as a Risk Factor for Congenital Anomalies. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22951

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


Freie Universität Berlin

5. Patino Mayer, Jan. Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease.

Degree: 2013, Freie Universität Berlin

 Little is known about the immune responses of newborns with congenital Chagas disease (CCD) or congenital toxoplasmosis (CT) but they probably differ to those seen… (more)

Subjects/Keywords: congenital Chagas; congenital toxoplasmosis; congenital transmission; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Patino Mayer, J. (2013). Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10561

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):

Patino Mayer, Jan. “Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease.” 2013. Thesis, Freie Universität Berlin. Accessed September 19, 2020. http://dx.doi.org/10.17169/refubium-10561.

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

MLA Handbook (7th Edition):

Patino Mayer, Jan. “Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease.” 2013. Web. 19 Sep 2020.

Vancouver:

Patino Mayer J. Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Sep 19]. Available from: http://dx.doi.org/10.17169/refubium-10561.

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

Council of Science Editors:

Patino Mayer J. Cytokine behaviour of pro- inflammatory IL-18, IFN-γ and counter- regulatory IL-10 in newborns with congenital Chagas disease. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-10561

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


Queensland University of Technology

6. Connor, Liam. Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences.

Degree: 2009, Queensland University of Technology

 The last twenty years has seen a significant improvement in the physical health of sufferers of Congenital Heart Disease (CHD) due to advances in medical… (more)

Subjects/Keywords: Congenital heart disease; thesis; doctoral

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APA (6th Edition):

Connor, L. (2009). Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/35794/

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):

Connor, Liam. “Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences.” 2009. Thesis, Queensland University of Technology. Accessed September 19, 2020. https://eprints.qut.edu.au/35794/.

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

MLA Handbook (7th Edition):

Connor, Liam. “Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences.” 2009. Web. 19 Sep 2020.

Vancouver:

Connor L. Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences. [Internet] [Thesis]. Queensland University of Technology; 2009. [cited 2020 Sep 19]. Available from: https://eprints.qut.edu.au/35794/.

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

Council of Science Editors:

Connor L. Adolescents with congenital heart disease: an exploration of psychosocial development, intra-hospital and familial experiences. [Thesis]. Queensland University of Technology; 2009. Available from: https://eprints.qut.edu.au/35794/

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


University of Alberta

7. Shearer, Kathleen. Quality of life in adolescents with congenital heart disease.

Degree: Master of Nursing, 2011, University of Alberta

 Technological advances for treatment of congenital heart disease (CHD) have led to decreases in mortality over the past thirty years. Persistent morbidity into adolescence and… (more)

Subjects/Keywords: Congenital; Adolescents; Disease; Heart

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APA (6th Edition):

Shearer, K. (2011). Quality of life in adolescents with congenital heart disease. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1j92g8593

Chicago Manual of Style (16th Edition):

Shearer, Kathleen. “Quality of life in adolescents with congenital heart disease.” 2011. Masters Thesis, University of Alberta. Accessed September 19, 2020. https://era.library.ualberta.ca/files/1j92g8593.

MLA Handbook (7th Edition):

Shearer, Kathleen. “Quality of life in adolescents with congenital heart disease.” 2011. Web. 19 Sep 2020.

Vancouver:

Shearer K. Quality of life in adolescents with congenital heart disease. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2020 Sep 19]. Available from: https://era.library.ualberta.ca/files/1j92g8593.

Council of Science Editors:

Shearer K. Quality of life in adolescents with congenital heart disease. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/1j92g8593


University of Alberta

8. Islam, Sunjidatul. Hospitalization and Readmission among Congenital Heart Disease Patients in Canada.

Degree: MS, Department of Public Health Sciences, 2014, University of Alberta

 The prevalence of congenital heart disease (CHD) is rising, particularly among adults. The rise is particularly prominent for CHD with complex lesions. The impact of… (more)

Subjects/Keywords: hospitalization; readmission; Congenital heart disease

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APA (6th Edition):

Islam, S. (2014). Hospitalization and Readmission among Congenital Heart Disease Patients in Canada. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1v53jx55m

Chicago Manual of Style (16th Edition):

Islam, Sunjidatul. “Hospitalization and Readmission among Congenital Heart Disease Patients in Canada.” 2014. Masters Thesis, University of Alberta. Accessed September 19, 2020. https://era.library.ualberta.ca/files/1v53jx55m.

MLA Handbook (7th Edition):

Islam, Sunjidatul. “Hospitalization and Readmission among Congenital Heart Disease Patients in Canada.” 2014. Web. 19 Sep 2020.

Vancouver:

Islam S. Hospitalization and Readmission among Congenital Heart Disease Patients in Canada. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2020 Sep 19]. Available from: https://era.library.ualberta.ca/files/1v53jx55m.

Council of Science Editors:

Islam S. Hospitalization and Readmission among Congenital Heart Disease Patients in Canada. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/1v53jx55m

9. 安達, 裕行. 日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism.

Degree: 博士(医学), 2017, Akita University / 秋田大学

 Objective: The prevalence of genetic mutations in congenital hypothyroidism (CH) remains undetermined. The objective of this study was to determine the prevalence of mutations in… (more)

Subjects/Keywords: congenital hypothyroidism; genes; mutation; prevalence

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APA (6th Edition):

安達, . (2017). 日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism. (Thesis). Akita University / 秋田大学. Retrieved from http://hdl.handle.net/10295/2513

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):

安達, 裕行. “日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism.” 2017. Thesis, Akita University / 秋田大学. Accessed September 19, 2020. http://hdl.handle.net/10295/2513.

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

MLA Handbook (7th Edition):

安達, 裕行. “日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism.” 2017. Web. 19 Sep 2020.

Vancouver:

安達 . 日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism. [Internet] [Thesis]. Akita University / 秋田大学; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10295/2513.

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

Council of Science Editors:

安達 . 日本人重症先天性甲状腺機能低下症患者における新規遺伝子異変の同定 : Identification of novel genetic mutations in Japanese patients with severe congenital hypothyroidism. [Thesis]. Akita University / 秋田大学; 2017. Available from: http://hdl.handle.net/10295/2513

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


University of Manchester

10. Han, Bing. Islet Pathobiology in Congenital Hyperinsulinism in Infancy.

Degree: 2017, University of Manchester

Congenital Hyperinsulinism of Infancy (CHI) is a potentially lethal condition caused by excessive, unregulated insulin release from pancreatic β-cells. It is a complex clinical condition… (more)

Subjects/Keywords: Congenital Hyperinsulinism; Islet Pathobiology

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APA (6th Edition):

Han, B. (2017). Islet Pathobiology in Congenital Hyperinsulinism in Infancy. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308829

Chicago Manual of Style (16th Edition):

Han, Bing. “Islet Pathobiology in Congenital Hyperinsulinism in Infancy.” 2017. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308829.

MLA Handbook (7th Edition):

Han, Bing. “Islet Pathobiology in Congenital Hyperinsulinism in Infancy.” 2017. Web. 19 Sep 2020.

Vancouver:

Han B. Islet Pathobiology in Congenital Hyperinsulinism in Infancy. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308829.

Council of Science Editors:

Han B. Islet Pathobiology in Congenital Hyperinsulinism in Infancy. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308829


University of Saskatchewan

11. Keir, Michelle 1981-. Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan.

Degree: 2019, University of Saskatchewan

 Background: The majority of patients born with congenital heart disease (CHD) now live to adulthood due to advanced surgical techniques and pediatric cardiology expertise. Facilitating… (more)

Subjects/Keywords: Adult Congenital Heart Disease; Transition

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APA (6th Edition):

Keir, M. 1. (2019). Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12052

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):

Keir, Michelle 1981-. “Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan.” 2019. Thesis, University of Saskatchewan. Accessed September 19, 2020. http://hdl.handle.net/10388/12052.

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

MLA Handbook (7th Edition):

Keir, Michelle 1981-. “Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan.” 2019. Web. 19 Sep 2020.

Vancouver:

Keir M1. Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10388/12052.

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

Council of Science Editors:

Keir M1. Adult Congenital Heart Disease: Assessing Barriers to Care in Saskatchewan. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12052

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


Leiden University

12. Joyce, Rhiannon Louise. Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research.

Degree: 2016, Leiden University

Congenital syphilis is a disease which still affects thousands of people throughout the world in a modern society. If untreated, congenital syphilis can be extremely… (more)

Subjects/Keywords: Congenital syphilis; Palaeopathology; Osteoarchaeology; Disease

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APA (6th Edition):

Joyce, R. L. (2016). Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research. (Masters Thesis). Leiden University. Retrieved from http://hdl.handle.net/1887/42385

Chicago Manual of Style (16th Edition):

Joyce, Rhiannon Louise. “Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research.” 2016. Masters Thesis, Leiden University. Accessed September 19, 2020. http://hdl.handle.net/1887/42385.

MLA Handbook (7th Edition):

Joyce, Rhiannon Louise. “Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research.” 2016. Web. 19 Sep 2020.

Vancouver:

Joyce RL. Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research. [Internet] [Masters thesis]. Leiden University; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1887/42385.

Council of Science Editors:

Joyce RL. Congenital syphilis in the past: Improving diagnostic criteria using clinical and palaeopathological research. [Masters Thesis]. Leiden University; 2016. Available from: http://hdl.handle.net/1887/42385

13. 서, 승조. Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?.

Degree: 2012, Ajou University

Although craniofacial asymmetry is frequently involved in the congenital muscular torticollis (CMT) patients who require surgical release, it has not been evaluated appropriately. Therefore, little… (more)

Subjects/Keywords: Congenital muscular torticollis; Craniofacial asymmetry

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APA (6th Edition):

서, . (2012). Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/7601 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012967

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):

서, 승조. “Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?.” 2012. Thesis, Ajou University. Accessed September 19, 2020. http://repository.ajou.ac.kr/handle/201003/7601 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012967.

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

MLA Handbook (7th Edition):

서, 승조. “Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?.” 2012. Web. 19 Sep 2020.

Vancouver:

서 . Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?. [Internet] [Thesis]. Ajou University; 2012. [cited 2020 Sep 19]. Available from: http://repository.ajou.ac.kr/handle/201003/7601 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012967.

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

Council of Science Editors:

서 . Is craniofacial asymmetry progressive in the untreated congenital muscular torticollis?. [Thesis]. Ajou University; 2012. Available from: http://repository.ajou.ac.kr/handle/201003/7601 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012967

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


Boston University

14. Leisner, Michelle. Pregnancy among women with congenital heart defects: outcomes for mother and child.

Degree: MS, Medical Sciences, 2019, Boston University

Congenital Heart Defects (CHDs), structural heart defects that are present at birth, are prevalent in approximately 1% of live births. While, historically, the presence of… (more)

Subjects/Keywords: Medicine; Congenital heart defects

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APA (6th Edition):

Leisner, M. (2019). Pregnancy among women with congenital heart defects: outcomes for mother and child. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/36600

Chicago Manual of Style (16th Edition):

Leisner, Michelle. “Pregnancy among women with congenital heart defects: outcomes for mother and child.” 2019. Masters Thesis, Boston University. Accessed September 19, 2020. http://hdl.handle.net/2144/36600.

MLA Handbook (7th Edition):

Leisner, Michelle. “Pregnancy among women with congenital heart defects: outcomes for mother and child.” 2019. Web. 19 Sep 2020.

Vancouver:

Leisner M. Pregnancy among women with congenital heart defects: outcomes for mother and child. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2144/36600.

Council of Science Editors:

Leisner M. Pregnancy among women with congenital heart defects: outcomes for mother and child. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/36600


University of Manchester

15. Eastwood, Lauren Elizabeth. Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism.

Degree: PhD, 2013, University of Manchester

 Islet transplantation has proved to be a useful treatment for Type 1 diabetes mellitus, but inadequate supplies of transplantable donor tissue have intensified the need… (more)

Subjects/Keywords: 616.4; Pancreatic Progenitors; Congenital Hyperinsulinism

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

APA (6th Edition):

Eastwood, L. E. (2013). Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/pancreatic-progenitor-cell-lines-derived-from-patients-with-congenital-hyperinsulinism(2f82b912-0a83-4bda-9086-355ae01330fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734197

Chicago Manual of Style (16th Edition):

Eastwood, Lauren Elizabeth. “Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism.” 2013. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. https://www.research.manchester.ac.uk/portal/en/theses/pancreatic-progenitor-cell-lines-derived-from-patients-with-congenital-hyperinsulinism(2f82b912-0a83-4bda-9086-355ae01330fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734197.

MLA Handbook (7th Edition):

Eastwood, Lauren Elizabeth. “Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism.” 2013. Web. 19 Sep 2020.

Vancouver:

Eastwood LE. Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Sep 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/pancreatic-progenitor-cell-lines-derived-from-patients-with-congenital-hyperinsulinism(2f82b912-0a83-4bda-9086-355ae01330fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734197.

Council of Science Editors:

Eastwood LE. Pancreatic progenitor cell lines derived from patients with congenital hyperinsulinism. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/pancreatic-progenitor-cell-lines-derived-from-patients-with-congenital-hyperinsulinism(2f82b912-0a83-4bda-9086-355ae01330fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734197


University of Sydney

16. White, Peter. Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds .

Degree: 2010, University of Sydney

 A form of congenital chondrodystrophy of unknown origin (CCUO), often referred to in Australia as acorn calf disease, was reported irregularly in beef cattle in… (more)

Subjects/Keywords: beef cattle; congenital; chondrodystrophy

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

APA (6th Edition):

White, P. (2010). Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/7009

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):

White, Peter. “Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds .” 2010. Thesis, University of Sydney. Accessed September 19, 2020. http://hdl.handle.net/2123/7009.

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

MLA Handbook (7th Edition):

White, Peter. “Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds .” 2010. Web. 19 Sep 2020.

Vancouver:

White P. Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds . [Internet] [Thesis]. University of Sydney; 2010. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2123/7009.

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

Council of Science Editors:

White P. Studies of the epidemiology and risk factors involved in the pathogenesis of congenital chondrodystrophy of unknown origin in Australian beef herds . [Thesis]. University of Sydney; 2010. Available from: http://hdl.handle.net/2123/7009

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


University of Melbourne

17. Jackling, Felicity Claire. A genetic investigation of congenital defects in alpacas.

Degree: 2013, University of Melbourne

 The aim of this PhD project was to understand the genetic mechanisms contributing to congenital defects in alpacas. Alpaca veterinarians report a prevalence of congenital(more)

Subjects/Keywords: genetics; congenital defects; alpacas; mapping

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APA (6th Edition):

Jackling, F. C. (2013). A genetic investigation of congenital defects in alpacas. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39780

Chicago Manual of Style (16th Edition):

Jackling, Felicity Claire. “A genetic investigation of congenital defects in alpacas.” 2013. Doctoral Dissertation, University of Melbourne. Accessed September 19, 2020. http://hdl.handle.net/11343/39780.

MLA Handbook (7th Edition):

Jackling, Felicity Claire. “A genetic investigation of congenital defects in alpacas.” 2013. Web. 19 Sep 2020.

Vancouver:

Jackling FC. A genetic investigation of congenital defects in alpacas. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11343/39780.

Council of Science Editors:

Jackling FC. A genetic investigation of congenital defects in alpacas. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/39780


University of Manchester

18. Eastwood, Lauren. Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism.

Degree: 2012, University of Manchester

 Islet transplantation has proved to be a useful treatment for Type 1 diabetes mellitus, but inadequate supplies of transplantable donor tissue have intensified the need… (more)

Subjects/Keywords: Pancreatic Progenitors; Congenital Hyperinsulinism

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

APA (6th Edition):

Eastwood, L. (2012). Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183653

Chicago Manual of Style (16th Edition):

Eastwood, Lauren. “Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism.” 2012. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183653.

MLA Handbook (7th Edition):

Eastwood, Lauren. “Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism.” 2012. Web. 19 Sep 2020.

Vancouver:

Eastwood L. Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183653.

Council of Science Editors:

Eastwood L. Pancreatic Progenitor Cell Lines Derived from Patients with Congenital Hyperinsulinism. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:183653

19. Halling, Veronica. Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie.

Degree: Health and Culture, 2012, University West

  Introduction : Structural cardiac malformations affects 0.8-1% of children born worldwide, in Sweden 800-1000 children per year. Most children with congenital heart disease and… (more)

Subjects/Keywords: experience; heart defects congenital; heart disease congenital; parents and parenting.

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

APA (6th Edition):

Halling, V. (2012). Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie. (Thesis). University West. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-4783

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):

Halling, Veronica. “Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie.” 2012. Thesis, University West. Accessed September 19, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-4783.

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

MLA Handbook (7th Edition):

Halling, Veronica. “Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie.” 2012. Web. 19 Sep 2020.

Vancouver:

Halling V. Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie. [Internet] [Thesis]. University West; 2012. [cited 2020 Sep 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-4783.

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

Council of Science Editors:

Halling V. Att vara förälder till ett barn med medfött hjärtfel : en litteraturstudie. [Thesis]. University West; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-4783

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

20. Boer, Lonneke de. Characteristics of Sotos syndrome.

Degree: 2005, Leiden University, Leiden University Medical Center, Dept. of Pediatrics

Subjects/Keywords: Congenital defects; Congenital defects

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

APA (6th Edition):

Boer, L. d. (2005). Characteristics of Sotos syndrome. (Doctoral Dissertation). Leiden University, Leiden University Medical Center, Dept. of Pediatrics. Retrieved from http://hdl.handle.net/1887/4565

Chicago Manual of Style (16th Edition):

Boer, Lonneke de. “Characteristics of Sotos syndrome.” 2005. Doctoral Dissertation, Leiden University, Leiden University Medical Center, Dept. of Pediatrics. Accessed September 19, 2020. http://hdl.handle.net/1887/4565.

MLA Handbook (7th Edition):

Boer, Lonneke de. “Characteristics of Sotos syndrome.” 2005. Web. 19 Sep 2020.

Vancouver:

Boer Ld. Characteristics of Sotos syndrome. [Internet] [Doctoral dissertation]. Leiden University, Leiden University Medical Center, Dept. of Pediatrics; 2005. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1887/4565.

Council of Science Editors:

Boer Ld. Characteristics of Sotos syndrome. [Doctoral Dissertation]. Leiden University, Leiden University Medical Center, Dept. of Pediatrics; 2005. Available from: http://hdl.handle.net/1887/4565


University of Manchester

21. Mal, Walaa Abdulsamad. The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy.

Degree: 2019, University of Manchester

Congenital Hyperinsulinism in Infancy (CHI) is a potentially lethal disease that leads to severe hypoglycaemia in children due to the impaired insulin release by β-cells.… (more)

Subjects/Keywords: Islets; Congenital Hyperinsulinism; Islet organization; Diffuse Congenital Hyperinsulinism; Focal Congenital Hyperinsulinism; Islet basement membranes; Collagen IV; laminin 511; Blood vessels

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

APA (6th Edition):

Mal, W. A. (2019). The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318505

Chicago Manual of Style (16th Edition):

Mal, Walaa Abdulsamad. “The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy.” 2019. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318505.

MLA Handbook (7th Edition):

Mal, Walaa Abdulsamad. “The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy.” 2019. Web. 19 Sep 2020.

Vancouver:

Mal WA. The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318505.

Council of Science Editors:

Mal WA. The Organization and Structure of Islets of Langerhans in Congenital Hyperinsulinism in Infancy. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318505


University of Helsinki

22. Karstunen, Emma. Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland.

Degree: Medicinska fakulteten, 2017, University of Helsinki

 Major extracardiac malformations are more common than previously 67 reported and found in 2/3 of cases with CDH and heart defect. Prenatal detection rates 68… (more)

Subjects/Keywords: congenital diaphragmatic hernia; CDH; congenital heart defect; congenital heart anomaly; extracardiac anomaly; prenatal diagnosis; survival; Paediatrics; Lastentaudit; Barnsjukdomar

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

APA (6th Edition):

Karstunen, E. (2017). Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/225986

Chicago Manual of Style (16th Edition):

Karstunen, Emma. “Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland.” 2017. Masters Thesis, University of Helsinki. Accessed September 19, 2020. http://hdl.handle.net/10138/225986.

MLA Handbook (7th Edition):

Karstunen, Emma. “Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland.” 2017. Web. 19 Sep 2020.

Vancouver:

Karstunen E. Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10138/225986.

Council of Science Editors:

Karstunen E. Congenital diaphragmatic hernia with 1 heart defect has a higher risk of major extracardiac malformations than expected : 10-year national cohort from Finland. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/225986


University of Manchester

23. Mal, Walaa. The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy.

Degree: PhD, 2019, University of Manchester

Congenital Hyperinsulinism in Infancy (CHI) is a potentially lethal disease that leads to severe hypoglycaemia in children due to the impaired insulin release by β-cells.… (more)

Subjects/Keywords: Collagen IV; Blood vessels; laminin 511; Islet basement membranes; Focal Congenital Hyperinsulinism; Diffuse Congenital Hyperinsulinism; Islet organization; Congenital Hyperinsulinism; Islets

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

APA (6th Edition):

Mal, W. (2019). The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-organization-and-structure-of-islets-of-langerhans-in-congenital-hyperinsulinism-in-infancy(ae13a9d1-7a40-4fe2-a128-0d929a67e74f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799450

Chicago Manual of Style (16th Edition):

Mal, Walaa. “The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy.” 2019. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. https://www.research.manchester.ac.uk/portal/en/theses/the-organization-and-structure-of-islets-of-langerhans-in-congenital-hyperinsulinism-in-infancy(ae13a9d1-7a40-4fe2-a128-0d929a67e74f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799450.

MLA Handbook (7th Edition):

Mal, Walaa. “The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy.” 2019. Web. 19 Sep 2020.

Vancouver:

Mal W. The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Sep 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-organization-and-structure-of-islets-of-langerhans-in-congenital-hyperinsulinism-in-infancy(ae13a9d1-7a40-4fe2-a128-0d929a67e74f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799450.

Council of Science Editors:

Mal W. The organization and structure of islets of Langerhans in Congenital Hyperinsulinism in Infancy. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-organization-and-structure-of-islets-of-langerhans-in-congenital-hyperinsulinism-in-infancy(ae13a9d1-7a40-4fe2-a128-0d929a67e74f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799450


UCLA

24. Yourshaw, Michael. Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain.

Degree: Human Genetics, 2013, UCLA

 High throughput, massively parallel DNA sequencing provides a powerful technology to study the human genome and to identify variations in DNA that cause disease. Sequencing… (more)

Subjects/Keywords: Genetics; congenital diarrheal disorders; exome; pontocerebellar hypoplasia

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APA (6th Edition):

Yourshaw, M. (2013). Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6cf2z4cq

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):

Yourshaw, Michael. “Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain.” 2013. Thesis, UCLA. Accessed September 19, 2020. http://www.escholarship.org/uc/item/6cf2z4cq.

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

MLA Handbook (7th Edition):

Yourshaw, Michael. “Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain.” 2013. Web. 19 Sep 2020.

Vancouver:

Yourshaw M. Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain. [Internet] [Thesis]. UCLA; 2013. [cited 2020 Sep 19]. Available from: http://www.escholarship.org/uc/item/6cf2z4cq.

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

Council of Science Editors:

Yourshaw M. Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/6cf2z4cq

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


Drexel University

25. Tse, Tiffany K. Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults.

Degree: 2016, Drexel University

 Single ventricular defects of the heart occur in 5 out of 100,000 live births. This type of congenital heart defect does not provide a sustainable… (more)

Subjects/Keywords: Biomedical engineering; Electrocardiography; Congenital heart disease

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APA (6th Edition):

Tse, T. K. (2016). Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7114

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):

Tse, Tiffany K. “Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults.” 2016. Thesis, Drexel University. Accessed September 19, 2020. http://hdl.handle.net/1860/idea:7114.

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

MLA Handbook (7th Edition):

Tse, Tiffany K. “Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults.” 2016. Web. 19 Sep 2020.

Vancouver:

Tse TK. Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults. [Internet] [Thesis]. Drexel University; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1860/idea:7114.

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

Council of Science Editors:

Tse TK. Externally Applied Pneumatic Compression as a Therapy for Fontan Patients: A Comfort Level Assessment on Adults. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7114

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


Drexel University

26. Pastor, Steven. Analysis of Genomic Structures Involved in 22q Deletion Syndrome.

Degree: 2018, Drexel University

 The 22q11.2 Deletion Syndrome (22q11DS) is a congenital malformation disorder and the most frequent microdeletion syndrome in humans [1]. It has a prevalence of 1… (more)

Subjects/Keywords: Medical sciences; Bioinformatics; Congenital heart disease

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APA (6th Edition):

Pastor, S. (2018). Analysis of Genomic Structures Involved in 22q Deletion Syndrome. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A9333

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):

Pastor, Steven. “Analysis of Genomic Structures Involved in 22q Deletion Syndrome.” 2018. Thesis, Drexel University. Accessed September 19, 2020. https://idea.library.drexel.edu/islandora/object/idea%3A9333.

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

MLA Handbook (7th Edition):

Pastor, Steven. “Analysis of Genomic Structures Involved in 22q Deletion Syndrome.” 2018. Web. 19 Sep 2020.

Vancouver:

Pastor S. Analysis of Genomic Structures Involved in 22q Deletion Syndrome. [Internet] [Thesis]. Drexel University; 2018. [cited 2020 Sep 19]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9333.

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

Council of Science Editors:

Pastor S. Analysis of Genomic Structures Involved in 22q Deletion Syndrome. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9333

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

27. Kellaway, Sophie. Stem cells from patients with Congenital Hyperinsulinism.

Degree: 2016, University of Manchester

 Diabetes and congenital hyperinsulinism (CHI) are severe diseases affecting the pancreas. Current models for testing drugs to treat these diseases are in vivo in rodents… (more)

Subjects/Keywords: stem cells; pancreas; beta cells; congenital hyperinsulinism

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

APA (6th Edition):

Kellaway, S. (2016). Stem cells from patients with Congenital Hyperinsulinism. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305721

Chicago Manual of Style (16th Edition):

Kellaway, Sophie. “Stem cells from patients with Congenital Hyperinsulinism.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 19, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305721.

MLA Handbook (7th Edition):

Kellaway, Sophie. “Stem cells from patients with Congenital Hyperinsulinism.” 2016. Web. 19 Sep 2020.

Vancouver:

Kellaway S. Stem cells from patients with Congenital Hyperinsulinism. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305721.

Council of Science Editors:

Kellaway S. Stem cells from patients with Congenital Hyperinsulinism. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305721

28. Singh,Praveen R. Dermatoglyphic variation in congenital heart diseases;.

Degree: Anatomy, 2015, Gujarat University

Abstract Not Available

Data not available

Advisors/Committee Members: Shah,G V.

Subjects/Keywords: Congenital; Dermatoglyphic; Photographs

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

APA (6th Edition):

R, S. (2015). Dermatoglyphic variation in congenital heart diseases;. (Thesis). Gujarat University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/48698

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):

R, Singh,Praveen. “Dermatoglyphic variation in congenital heart diseases;.” 2015. Thesis, Gujarat University. Accessed September 19, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/48698.

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

MLA Handbook (7th Edition):

R, Singh,Praveen. “Dermatoglyphic variation in congenital heart diseases;.” 2015. Web. 19 Sep 2020.

Vancouver:

R S. Dermatoglyphic variation in congenital heart diseases;. [Internet] [Thesis]. Gujarat University; 2015. [cited 2020 Sep 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/48698.

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

Council of Science Editors:

R S. Dermatoglyphic variation in congenital heart diseases;. [Thesis]. Gujarat University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/48698

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


Addis Ababa University

29. WORKINEH, DIRIBA. Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives .

Degree: 2014, Addis Ababa University

 Abstract Oral contraceptives are widely used and are generally safe and effective for many women. Oral contraceptives are known also as the Pill, POP, COCPs,… (more)

Subjects/Keywords: Oral contraceptive; congenital limb reduction defects; pregnancy.

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

APA (6th Edition):

WORKINEH, D. (2014). Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/5229

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):

WORKINEH, DIRIBA. “Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives .” 2014. Thesis, Addis Ababa University. Accessed September 19, 2020. http://etd.aau.edu.et/dspace/handle/123456789/5229.

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

MLA Handbook (7th Edition):

WORKINEH, DIRIBA. “Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives .” 2014. Web. 19 Sep 2020.

Vancouver:

WORKINEH D. Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives . [Internet] [Thesis]. Addis Ababa University; 2014. [cited 2020 Sep 19]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/5229.

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

Council of Science Editors:

WORKINEH D. Project paper on risk of Congenital Limb Reduction Defects Associated with in utero exposure to Oral Contraceptives . [Thesis]. Addis Ababa University; 2014. Available from: http://etd.aau.edu.et/dspace/handle/123456789/5229

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


Harvard University

30. Simons, Emily. Systematic Review of the Manifestations of Congenital Rubella Syndrome.

Degree: Doctor of Medicine, 2017, Harvard University

Congenital rubella syndrome (CRS) continues to cause disability among unvaccinated populations, particularly in the 62 countries yet to introduce rubella vaccine and in immunized populations… (more)

Subjects/Keywords: congenital rubella syndrome; vaccination; disease burden

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

APA (6th Edition):

Simons, E. (2017). Systematic Review of the Manifestations of Congenital Rubella Syndrome. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:40621358

Chicago Manual of Style (16th Edition):

Simons, Emily. “Systematic Review of the Manifestations of Congenital Rubella Syndrome.” 2017. Doctoral Dissertation, Harvard University. Accessed September 19, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:40621358.

MLA Handbook (7th Edition):

Simons, Emily. “Systematic Review of the Manifestations of Congenital Rubella Syndrome.” 2017. Web. 19 Sep 2020.

Vancouver:

Simons E. Systematic Review of the Manifestations of Congenital Rubella Syndrome. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Sep 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:40621358.

Council of Science Editors:

Simons E. Systematic Review of the Manifestations of Congenital Rubella Syndrome. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:40621358

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