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Sian Ellard

Showing results (111-120 of 439) with videos related to

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European Journal of Endocrinology|March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinismSo Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care|March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick daysEthel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Diabetes|October 19, 2007
An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinismKhalid Hussain, Sarah E Flanagan, Virpi V Smith, et al.
European Journal of Endocrinology|January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinismRitika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2014
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapyHuseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, et al.
Clinical Endocrinology|June 4, 2016
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in TurkeyBelma Haliloglu, Gerald Hysenaj, Zeynep Atay, 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|March 29, 2018
p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid CancerChey Loveday, Katherine Josephs, Daniel Chubb, 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.
Diabetes|June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalitiesOscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
Pageof 44

Showing results (111-120 of 439) with videos related to

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Pageof 44
European Journal of Endocrinology|March 23, 2011
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinismSo Eun Park, Sarah E Flanagan, Khalid Hussain, et al.
Diabetes Care|March 6, 2007
Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick daysEthel Codner, Sarah E Flanagan, Francisca Ugarte, et al.
Diabetes|October 19, 2007
An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinismKhalid Hussain, Sarah E Flanagan, Virpi V Smith, et al.
European Journal of Endocrinology|January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinismRitika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2014
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapyHuseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, et al.
Clinical Endocrinology|June 4, 2016
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in TurkeyBelma Haliloglu, Gerald Hysenaj, Zeynep Atay, 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|March 29, 2018
p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid CancerChey Loveday, Katherine Josephs, Daniel Chubb, 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.
Diabetes|June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalitiesOscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
Pageof 44