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Archives of Disease in Childhood|February 6, 2009
Hyperinsulinaemic hypoglycaemiaR R Kapoor, S E Flanagan, C James, 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.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.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.Diabetologia|June 16, 2011
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutationsR R Kapoor, S E Flanagan, C T James, et al.Journal of Medical Genetics|March 4, 2009
The genetic basis of congenital hyperinsulinismC James, R R Kapoor, D Ismail, et al.Indian Journal of Pediatrics|April 20, 2010
KCNJ11 activating mutation in an Indian family with remitting and relapsing diabetesV V Khadilkar, A V Khadilkar, R R Kapoor, et al.European Journal of Endocrinology|February 19, 2010
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutationsS E Flanagan, R R Kapoor, G Mali, et al.Pediatric Diabetes|March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotoniaS E Flanagan, F Vairo, M B Johnson, et al.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.Pageof 220