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Sarah E Flanagan

Showing results (71-80 of 231) with videos related to

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Diabetes|December 11, 2012
GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiencyElisa De Franco, Charles Shaw-Smith, Sarah E Flanagan, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 22, 2018
Focal Congenital Hyperinsulinism as a Cause for Sudden Infant DeathAmish Chinoy, Indraneel Banerjee, Sarah E Flanagan, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 5, 2021
Octreotide-LAR is a Useful Alternative for the Management of Diazoxide-Responsive Congenital HyperinsulinismManjiri Pramod Karlekar, Vijaya Sarathi, Sneha Arya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Permanent neonatal diabetes mellitus in JordanMousa A Abujbara, Mohammed I Liswi, Mohammed S El-Khateeb, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 31, 2013
Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational ageVed Bhushan Arya, Sarah E Flanagan, Anitha Kumaran, et al.
Clinical Chemistry|September 10, 2016
Low IgE Is a Useful Tool to Identify STAT3 Gain-of-Function MutationsMatthew B Johnson, Sarah E Flanagan, Thomas B Martins, et al.
Diabetes|May 28, 2011
Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetesRoope Männikkö, Sarah E Flanagan, Xiuli Sim, et al.
Human Mutation|September 4, 2008
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinismSarah E Flanagan, Séverine Clauin, Christine Bellanné-Chantelot, et al.
JIMD Reports|February 23, 2013
Galactokinase deficiency in a patient with congenital hyperinsulinismMashbat Bayarchimeg, Dunia Ismail, Amanda Lam, et al.
Diabetologia|April 28, 2016
Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes riskNatascia Vedovato, Edward Cliff, Peter Proks, et al.
Pageof 24

Showing results (71-80 of 231) with videos related to

Sort By:
Pageof 24
Diabetes|December 11, 2012
GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiencyElisa De Franco, Charles Shaw-Smith, Sarah E Flanagan, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 22, 2018
Focal Congenital Hyperinsulinism as a Cause for Sudden Infant DeathAmish Chinoy, Indraneel Banerjee, Sarah E Flanagan, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 5, 2021
Octreotide-LAR is a Useful Alternative for the Management of Diazoxide-Responsive Congenital HyperinsulinismManjiri Pramod Karlekar, Vijaya Sarathi, Sneha Arya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Permanent neonatal diabetes mellitus in JordanMousa A Abujbara, Mohammed I Liswi, Mohammed S El-Khateeb, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 31, 2013
Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational ageVed Bhushan Arya, Sarah E Flanagan, Anitha Kumaran, et al.
Clinical Chemistry|September 10, 2016
Low IgE Is a Useful Tool to Identify STAT3 Gain-of-Function MutationsMatthew B Johnson, Sarah E Flanagan, Thomas B Martins, et al.
Diabetes|May 28, 2011
Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetesRoope Männikkö, Sarah E Flanagan, Xiuli Sim, et al.
Human Mutation|September 4, 2008
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinismSarah E Flanagan, Séverine Clauin, Christine Bellanné-Chantelot, et al.
JIMD Reports|February 23, 2013
Galactokinase deficiency in a patient with congenital hyperinsulinismMashbat Bayarchimeg, Dunia Ismail, Amanda Lam, et al.
Diabetologia|April 28, 2016
Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes riskNatascia Vedovato, Edward Cliff, Peter Proks, et al.
Pageof 24