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I Banerjee

Showing results (51-60 of 57) with videos related to

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Clinical Endocrinology|February 20, 2009
Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary glandP G Murray, C Hague, O Fafoula, et al.
European Journal of Endocrinology|March 8, 2011
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinismI Banerjee, M Skae, S E Flanagan, et al.
Journal of Molecular Endocrinology|October 3, 2013
Network analysis: a new approach to study endocrine disordersA Stevens, C De Leonibus, D Hanson, 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.
Diabetic Medicine : a Journal of the British Diabetic Association|December 16, 2014
Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communicationM Makov, G Chodick, K Mohnike, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
The Journal of Infection|December 3, 2025
Reactogenicity and immunogenicity following heterologous and homologous third dose COVID-19 vaccination in UK adolescents (Com-COV3): A randomised controlled non-inferiority trialE Kelly, M Greenland, P de Whalley, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Clinical Endocrinology|February 20, 2009
Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary glandP G Murray, C Hague, O Fafoula, et al.
European Journal of Endocrinology|March 8, 2011
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinismI Banerjee, M Skae, S E Flanagan, et al.
Journal of Molecular Endocrinology|October 3, 2013
Network analysis: a new approach to study endocrine disordersA Stevens, C De Leonibus, D Hanson, 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.
Diabetic Medicine : a Journal of the British Diabetic Association|December 16, 2014
Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communicationM Makov, G Chodick, K Mohnike, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
The Journal of Infection|December 3, 2025
Reactogenicity and immunogenicity following heterologous and homologous third dose COVID-19 vaccination in UK adolescents (Com-COV3): A randomised controlled non-inferiority trialE Kelly, M Greenland, P de Whalley, et al.
Pageof 6