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Genetic Testing and Molecular Biomarkers|July 21, 2010
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutationsSarah E Flanagan, Ann-Marie Patch, Sian EllardDiabetes 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.Methods in Molecular Biology (Clifton, N.J.)|November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channelSarah E Flanagan, Sian EllardIndian Pediatrics|July 17, 2012
Permanent neonatal diabetes caused by a novel mutationVandana Jain, Sarah E Flanagan, Sian EllardReviews in Endocrine & Metabolic Disorders|October 6, 2010
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11Emma L Edghill, Sarah E Flanagan, Sian EllardMethods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation surveyor: software for DNA sequence analysisJayne A L Minton, Sarah E Flanagan, Sian EllardThe Journal of Clinical Endocrinology and Metabolism|January 22, 2011
Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigreesSarah E Flanagan, Ann-Marie Patch, Jonathan M Locke, et al.Indian Pediatrics|October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two SiblingsAmit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital HyperinsulinismAyla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.Pageof 54