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Sian Ellard

Showing results (121-130 of 439) with videos related to

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Nature Reviews. Endocrinology|September 16, 2010
Focal congenital hyperinsulinism in a patient with septo-optic dysplasiaRaja Padidela, Ritika R Kapoor, Yuva Moyo, et al.
Hormone Research in Paediatrics|July 18, 2015
Variable Phenotype of Diabetes Mellitus in Siblings with a Homozygous PTF1A Enhancer MutationE Nazlı Gonc, Alev Ozon, Ayfer Alikasifoglu, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|December 20, 2021
Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 geneAtul Gupta, Chaithanya Reddy, Lokesh Saini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2006
Renal cysts and diabetes due to a heterozygous HNF-1beta gene deletionPhilipp Eller, Susanne Kaser, Karl Lhotta, et al.
Plos One|May 21, 2014
Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinismVed Bhushan Arya, Senthil Senniappan, Huseyin Demirbilek, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 22, 2020
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in TurkeyYasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, et al.
Diabetes 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.
Diabetologia|August 15, 2014
Neurogenin 3 is important but not essential for pancreatic islet development in humansOscar Rubio-Cabezas, Ethel Codner, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2014
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutationPratik Shah, Ved Bhushan Arya, Sarah E Flanagan, et al.
Clinical Endocrinology|December 19, 2020
Diagnostic RET genetic testing in 1,058 index patients: A UK centre perspectiveJonathan Mark Fussey, Joel Anthony Smith, Ruth Cleaver, et al.
Pageof 44

Showing results (121-130 of 439) with videos related to

Sort By:
Pageof 44
Nature Reviews. Endocrinology|September 16, 2010
Focal congenital hyperinsulinism in a patient with septo-optic dysplasiaRaja Padidela, Ritika R Kapoor, Yuva Moyo, et al.
Hormone Research in Paediatrics|July 18, 2015
Variable Phenotype of Diabetes Mellitus in Siblings with a Homozygous PTF1A Enhancer MutationE Nazlı Gonc, Alev Ozon, Ayfer Alikasifoglu, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|December 20, 2021
Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 geneAtul Gupta, Chaithanya Reddy, Lokesh Saini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2006
Renal cysts and diabetes due to a heterozygous HNF-1beta gene deletionPhilipp Eller, Susanne Kaser, Karl Lhotta, et al.
Plos One|May 21, 2014
Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinismVed Bhushan Arya, Senthil Senniappan, Huseyin Demirbilek, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 22, 2020
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in TurkeyYasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, et al.
Diabetes 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.
Diabetologia|August 15, 2014
Neurogenin 3 is important but not essential for pancreatic islet development in humansOscar Rubio-Cabezas, Ethel Codner, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2014
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutationPratik Shah, Ved Bhushan Arya, Sarah E Flanagan, et al.
Clinical Endocrinology|December 19, 2020
Diagnostic RET genetic testing in 1,058 index patients: A UK centre perspectiveJonathan Mark Fussey, Joel Anthony Smith, Ruth Cleaver, et al.
Pageof 44