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S E Flanagan

Showing results (11-20 of 30) with videos related to

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Diabetic Medicine : a Journal of the British Diabetic Association|June 26, 2013
The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case seriesS M McGlacken-Byrne, C P Hawkes, S E Flanagan, et al.
Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.
Pediatric Diabetes|March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotoniaS E Flanagan, F Vairo, M B Johnson, et al.
Neurology|July 27, 2007
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brainK Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports|March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinismSuresh Chandran, Fabian Yap Kok Peng, Victor Samuel Rajadurai, et al.
Diabetologia|March 13, 2008
A Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complicationsP Tammaro, S E Flanagan, B Zadek, et al.
Diabetes|May 22, 2016
Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 DiabetesK A Patel, R A Oram, S E Flanagan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 19, 2016
Psychiatric morbidity in children with KCNJ11 neonatal diabetesP Bowman, E Broadbridge, B A Knight, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 8, 2017
Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetesJ O Day, S E Flanagan, M H Shepherd, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|March 1, 2008
Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutationA S Slingerland, W Hurkx, K Noordam, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Diabetic Medicine : a Journal of the British Diabetic Association|June 26, 2013
The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case seriesS M McGlacken-Byrne, C P Hawkes, S E Flanagan, et al.
Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.
Pediatric Diabetes|March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotoniaS E Flanagan, F Vairo, M B Johnson, et al.
Neurology|July 27, 2007
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brainK Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports|March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinismSuresh Chandran, Fabian Yap Kok Peng, Victor Samuel Rajadurai, et al.
Diabetologia|March 13, 2008
A Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complicationsP Tammaro, S E Flanagan, B Zadek, et al.
Diabetes|May 22, 2016
Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 DiabetesK A Patel, R A Oram, S E Flanagan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 19, 2016
Psychiatric morbidity in children with KCNJ11 neonatal diabetesP Bowman, E Broadbridge, B A Knight, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 8, 2017
Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetesJ O Day, S E Flanagan, M H Shepherd, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|March 1, 2008
Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutationA S Slingerland, W Hurkx, K Noordam, et al.
Pageof 3