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

S E Flanagan

Showing results (1-10 of 30) with videos related to

Pageof 3
Sort By:
Journal of Diabetes Research|January 2, 2019
Future Roadmaps for Precision Medicine Applied to Diabetes: Rising to the Challenge of HeterogeneityP Bowman, S E Flanagan, A T Hattersley
Diabetes, Obesity & Metabolism|October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal periodA M Patch, S E Flanagan, C Boustred, et al.
Frontiers in Endocrinology|June 2, 2012
Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic HypoglycemiaS E Flanagan, R R Kapoor, V V Smith, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|July 31, 2012
Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a novel missense mutation, p.P1199L, in the ABCC8 geneO Oztekin, E Durmaz, S Kalay, et al.
Archives of Disease in Childhood|February 6, 2009
Hyperinsulinaemic hypoglycaemiaR R Kapoor, S E Flanagan, C James, et al.
Diabetologia|April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotypeS E Flanagan, E L Edghill, A L Gloyn, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Clinical Genetics|June 25, 2010
Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemiaS E Flanagan, R R Kapoor, I Banerjee, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Diabetes & Metabolism|May 4, 2013
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case reportG Catli, A Abaci, S E Flanagan, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Journal of Diabetes Research|January 2, 2019
Future Roadmaps for Precision Medicine Applied to Diabetes: Rising to the Challenge of HeterogeneityP Bowman, S E Flanagan, A T Hattersley
Diabetes, Obesity & Metabolism|October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal periodA M Patch, S E Flanagan, C Boustred, et al.
Frontiers in Endocrinology|June 2, 2012
Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic HypoglycemiaS E Flanagan, R R Kapoor, V V Smith, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|July 31, 2012
Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a novel missense mutation, p.P1199L, in the ABCC8 geneO Oztekin, E Durmaz, S Kalay, et al.
Archives of Disease in Childhood|February 6, 2009
Hyperinsulinaemic hypoglycaemiaR R Kapoor, S E Flanagan, C James, et al.
Diabetologia|April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotypeS E Flanagan, E L Edghill, A L Gloyn, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Clinical Genetics|June 25, 2010
Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemiaS E Flanagan, R R Kapoor, I Banerjee, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Diabetes & Metabolism|May 4, 2013
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case reportG Catli, A Abaci, S E Flanagan, et al.
Pageof 3