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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
January 15, 2003
Use of positron emission tomography in pharmacokinetic studies to investigate therapeutic advantage in a phase I study of 120-hour intravenous infusion XR5000
D J Propper, J de Bono, A Saleem, et al.
Diabetologia
|
June 5, 2012
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion
F H Sansbury, S E Flanagan, J A L Houghton, et al.
European Journal of Endocrinology
|
February 19, 2010
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations
S E Flanagan, R R Kapoor, G Mali, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2000
No evidence for linkage at candidate type 2 diabetes susceptibility loci on chromosomes 12 and 20 in United Kingdom Caucasians
T M Frayling, M I McCarthy, M Walker, et al.
Kidney International
|
March 18, 2000
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta
C Bingham, S Ellard, L Allen, et al.
Diabetologia
|
February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patients
L E Docherty, S Kabwama, A Lehmann, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delay
M Balasubramanian, J P H Shield, C L Acerini, et al.
European Journal of Human Genetics : EJHG
|
March 8, 2018
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy
K J Low, K Stals, R Caswell, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 24, 2006
Asian MODY: are we missing an important diagnosis?
J R Porter, J J Rangasami, S Ellard, et al.
Diabetes
|
April 1, 1997
Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K
T M Frayling, M P Bulamn, S Ellard, et al.
Page
of 15
Search research articles
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Showing results (121-130 of 144) with videos related to
Sort By:
Page
of 15
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
January 15, 2003
Use of positron emission tomography in pharmacokinetic studies to investigate therapeutic advantage in a phase I study of 120-hour intravenous infusion XR5000
D J Propper, J de Bono, A Saleem, et al.
Diabetologia
|
June 5, 2012
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion
F H Sansbury, S E Flanagan, J A L Houghton, et al.
European Journal of Endocrinology
|
February 19, 2010
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations
S E Flanagan, R R Kapoor, G Mali, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2000
No evidence for linkage at candidate type 2 diabetes susceptibility loci on chromosomes 12 and 20 in United Kingdom Caucasians
T M Frayling, M I McCarthy, M Walker, et al.
Kidney International
|
March 18, 2000
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta
C Bingham, S Ellard, L Allen, et al.
Diabetologia
|
February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patients
L E Docherty, S Kabwama, A Lehmann, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delay
M Balasubramanian, J P H Shield, C L Acerini, et al.
European Journal of Human Genetics : EJHG
|
March 8, 2018
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy
K J Low, K Stals, R Caswell, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 24, 2006
Asian MODY: are we missing an important diagnosis?
J R Porter, J J Rangasami, S Ellard, et al.
Diabetes
|
April 1, 1997
Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K
T M Frayling, M P Bulamn, S Ellard, et al.
Page
of 15