Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sarah E Flanagan

Showing results (61-70 of 231) with videos related to

Pageof 24
Sort By:
Diabetes Care|November 21, 2007
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutationsMeena Rafiq, Sarah E Flanagan, Ann-Marie Patch, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 9, 2017
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic HypoglycemiaBelma Haliloğlu, Heybet Tüzün, Sarah E. Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2009
An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1Tim J Craig, Kenju Shimomura, Reinhard W Holl, et al.
Diabetologia|August 15, 2014
Neurogenin 3 is important but not essential for pancreatic islet development in humansOscar Rubio-Cabezas, Ethel Codner, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2014
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutationPratik Shah, Ved Bhushan Arya, Sarah E Flanagan, et al.
Journal of Diabetes Investigation|March 10, 2025
Two cases of neonatal hyperglycemia caused by a homozygous COQ9 stop-gain variantRussell Donis, Maryam Al Badi, Nadia Alhashmi, et al.
Hormone Research in Paediatrics|May 14, 2016
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and HemihypertrophyPınar Kocaay, Zeynep Şiklar, Sian Ellard, et al.
BMC Research Notes|August 14, 2015
Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemiaSenthil Senniappan, Atefeh Sadeghizadeh, Sarah E Flanagan, et al.
European Journal of Endocrinology|June 1, 2012
Amino acid properties may be useful in predicting clinical outcome in patients with Kir6.2 neonatal diabetesClementine S Fraser, Oscar Rubio-Cabezas, Jennifer A Littlechild, et al.
Pediatric Diabetes|January 8, 2013
Thiamine responsive megaloblastic anemia: a novel SLC19A2 compound heterozygous mutation in two siblingsEnza Mozzillo, Daniela Melis, Mariateresa Falco, et al.
Pageof 24

Showing results (61-70 of 231) with videos related to

Sort By:
Pageof 24
Diabetes Care|November 21, 2007
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutationsMeena Rafiq, Sarah E Flanagan, Ann-Marie Patch, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 9, 2017
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic HypoglycemiaBelma Haliloğlu, Heybet Tüzün, Sarah E. Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2009
An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1Tim J Craig, Kenju Shimomura, Reinhard W Holl, et al.
Diabetologia|August 15, 2014
Neurogenin 3 is important but not essential for pancreatic islet development in humansOscar Rubio-Cabezas, Ethel Codner, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2014
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutationPratik Shah, Ved Bhushan Arya, Sarah E Flanagan, et al.
Journal of Diabetes Investigation|March 10, 2025
Two cases of neonatal hyperglycemia caused by a homozygous COQ9 stop-gain variantRussell Donis, Maryam Al Badi, Nadia Alhashmi, et al.
Hormone Research in Paediatrics|May 14, 2016
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and HemihypertrophyPınar Kocaay, Zeynep Şiklar, Sian Ellard, et al.
BMC Research Notes|August 14, 2015
Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemiaSenthil Senniappan, Atefeh Sadeghizadeh, Sarah E Flanagan, et al.
European Journal of Endocrinology|June 1, 2012
Amino acid properties may be useful in predicting clinical outcome in patients with Kir6.2 neonatal diabetesClementine S Fraser, Oscar Rubio-Cabezas, Jennifer A Littlechild, et al.
Pediatric Diabetes|January 8, 2013
Thiamine responsive megaloblastic anemia: a novel SLC19A2 compound heterozygous mutation in two siblingsEnza Mozzillo, Daniela Melis, Mariateresa Falco, et al.
Pageof 24