Search research articles
Contact Us
Filters
Showing results (11-20 of 30) with videos related to
Page
of 3
Sort By:
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 26, 2013
The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case series
S M McGlacken-Byrne, C P Hawkes, S E Flanagan, et al.
Diabetologia
|
October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODY
P 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 hypotonia
S 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 brain
K Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism
Suresh 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 complications
P 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 Diabetes
K 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 diabetes
P 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 diabetes
J 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 mutation
A S Slingerland, W Hurkx, K Noordam, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 26, 2013
The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case series
S M McGlacken-Byrne, C P Hawkes, S E Flanagan, et al.
Diabetologia
|
October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODY
P 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 hypotonia
S 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 brain
K Shimomura, F Hörster, H de Wet, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
March 12, 2014
Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism
Suresh 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 complications
P 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 Diabetes
K 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 diabetes
P 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 diabetes
J 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 mutation
A S Slingerland, W Hurkx, K Noordam, et al.
Page
of 3