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Reviews in Endocrine & Metabolic Disorders|September 30, 2010
Pancreatic β-cell KATP channels: Hypoglycaemia and hyperglycaemiaKate Bennett, Chela James, Khalid Hussain
Nature Clinical Practice. Endocrinology & Metabolism|January 24, 2009
Advances in the diagnosis and management of hyperinsulinemic hypoglycemiaRitika R Kapoor, Chela James, Khalid Hussain
Endocrine Development|March 19, 2009
Hyperinsulinism in developmental syndromesRitika R Kapoor, Chela James, Khalid Hussain
Journal of Inherited Metabolic Disease|January 11, 2012
Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and managementSenthil Senniappan, Balasubramaniam Shanti, Chela James, et al.
Development (Cambridge, England)|August 6, 2003
Role of Islet1 in the patterning of murine dentitionThimios A Mitsiadis, Irene Angeli, Chela James, et al.
Pediatric Diabetes|April 27, 2011
Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase geneKate Bennett, Chela James, Angham Mutair, 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 Endocrinology & Metabolism : JPEM|August 10, 2011
A single base-pair deletion in the WFS1 gene causes Wolfram syndromeKatherine Pitt, Chela James, Inderpal S Kochar, et al.
Cell Stem Cell|October 21, 2020
Mitochondrial Potentiation Ameliorates Age-Related Heterogeneity in Hematopoietic Stem Cell FunctionEls Mansell, Valgardur Sigurdsson, Elitza Deltcheva, et al.
Developmental Biology|August 20, 2005
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1Sarah Ivins, Kelly Lammerts van Beuren, Catherine Roberts, et al.
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