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Sarah E Flanagan

Showing results (31-40 of 230) with videos related to

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Diabetes Research and Clinical Practice|October 31, 2012
Permanent neonatal diabetes caused by a novel mutation in the INS geneGonul Catli, Ayhan Abaci, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 17, 2014
A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infantErdem Durmaz, Sarah E Flanagan, Mesut Parlak, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Extremely rare cause of congenital diarrhea: enteric anendocrinosisErsin Sayar, Ali Islek, Aygen Yilmaz, et al.
European Journal of Pediatrics|June 13, 2008
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapyVerena M Wagner, Britta Kremke, Olaf Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism|May 7, 2009
3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivityRitika R Kapoor, Chela James, Sarah E Flanagan, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 3, 2013
Chromogranin-A staining reveals enteric anendocrinosis in unexplained congenital diarrheaErsin Sayar, Aygen Yilmaz, Ali Islek, et al.
Diabetes Research and Clinical Practice|October 14, 2014
Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosisYotsapon Thewjitcharoen, Ekgaluck Wanothayaroj, Thep Himathongkam, et al.
Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 10, 2018
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F <i>ABCC8</i> MutationEmregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 28, 2015
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi familyOmer Babiker, Sarah E Flanagan, Sian Ellard, et al.
Pageof 23

Showing results (31-40 of 230) with videos related to

Sort By:
Pageof 23
Diabetes Research and Clinical Practice|October 31, 2012
Permanent neonatal diabetes caused by a novel mutation in the INS geneGonul Catli, Ayhan Abaci, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 17, 2014
A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infantErdem Durmaz, Sarah E Flanagan, Mesut Parlak, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 19, 2013
Extremely rare cause of congenital diarrhea: enteric anendocrinosisErsin Sayar, Ali Islek, Aygen Yilmaz, et al.
European Journal of Pediatrics|June 13, 2008
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapyVerena M Wagner, Britta Kremke, Olaf Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism|May 7, 2009
3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivityRitika R Kapoor, Chela James, Sarah E Flanagan, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 3, 2013
Chromogranin-A staining reveals enteric anendocrinosis in unexplained congenital diarrheaErsin Sayar, Aygen Yilmaz, Ali Islek, et al.
Diabetes Research and Clinical Practice|October 14, 2014
Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosisYotsapon Thewjitcharoen, Ekgaluck Wanothayaroj, Thep Himathongkam, et al.
Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 10, 2018
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F <i>ABCC8</i> MutationEmregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 28, 2015
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi familyOmer Babiker, Sarah E Flanagan, Sian Ellard, et al.
Pageof 23