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Sarah E Flanagan

Showing results (11-20 of 230) with videos related to

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Clinical Endocrinology|August 20, 2011
Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 geneRitika R Kapoor, Sarah E Flanagan, Sian Ellard, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 19, 2015
Anemia in a Child with Deafness: Be Vigilant for a Rare Cause!Mohammed Ramzan, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital HyperinsulinismAyla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.
Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.
Diabetes Research and Clinical Practice|July 4, 2012
Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian childrenCresio Alves, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 29, 2015
Nifedipine in Congenital Hyperinsulinism - A Case ReportPapiya Khawash, Khalid Hussain, Sarah E Flanagan, et al.
Diabetes Care|January 26, 2013
Comment on: Khurana et al. The diagnosis of neonatal diabetes in a mother at 25 years of age. Diabetes Care 2012;35:e59Ali J Chakera, Sarah E Flanagan, Sian Ellard, et al.
Current Diabetes Reports|March 20, 2019
Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune DiabetesMatthew B Johnson, Karen Cerosaletti, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 30, 2018
Diazoxide toxicity in a child with persistent hyperinsulinemic hypoglycemia of infancy: mixed hyperglycemic hyperosmolar coma and ketoacidosisPragya Mangla, Khalid Hussain, Sian Ellard, et al.
Hormone Research in Paediatrics|March 11, 2010
Congenital hyperinsulinism due to a compound heterozygous ABCC8 mutation with spontaneous resolution at eight weeksAnitha Kumaran, Ritika R Kapoor, Sarah E Flanagan, et al.
Pageof 23

Showing results (11-20 of 230) with videos related to

Sort By:
Pageof 23
Clinical Endocrinology|August 20, 2011
Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 geneRitika R Kapoor, Sarah E Flanagan, Sian Ellard, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 19, 2015
Anemia in a Child with Deafness: Be Vigilant for a Rare Cause!Mohammed Ramzan, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital HyperinsulinismAyla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.
Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.
Diabetes Research and Clinical Practice|July 4, 2012
Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian childrenCresio Alves, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 29, 2015
Nifedipine in Congenital Hyperinsulinism - A Case ReportPapiya Khawash, Khalid Hussain, Sarah E Flanagan, et al.
Diabetes Care|January 26, 2013
Comment on: Khurana et al. The diagnosis of neonatal diabetes in a mother at 25 years of age. Diabetes Care 2012;35:e59Ali J Chakera, Sarah E Flanagan, Sian Ellard, et al.
Current Diabetes Reports|March 20, 2019
Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune DiabetesMatthew B Johnson, Karen Cerosaletti, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 30, 2018
Diazoxide toxicity in a child with persistent hyperinsulinemic hypoglycemia of infancy: mixed hyperglycemic hyperosmolar coma and ketoacidosisPragya Mangla, Khalid Hussain, Sian Ellard, et al.
Hormone Research in Paediatrics|March 11, 2010
Congenital hyperinsulinism due to a compound heterozygous ABCC8 mutation with spontaneous resolution at eight weeksAnitha Kumaran, Ritika R Kapoor, Sarah E Flanagan, et al.
Pageof 23