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Archives of Disease in Childhood
|
August 24, 2004
Weight differences in Plymouth toddlers compared to the British Growth Reference Population
E Stenhouse, D E Wright, A T Hattersley, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 11, 2009
Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes
O Rubio-Cabezas, E L Edghill, J Argente, et al.
Diabetologia
|
January 12, 2007
The long-term impact on offspring of exposure to hyperglycaemia in utero due to maternal glucokinase gene mutations
R Singh, E R Pearson, P M Clark, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 8, 2009
Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation
G Spyer, K M Macleod, M Shepherd, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
April 25, 2009
A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients
M Shepherd, B Shields, S Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 5, 2002
Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics
K R Owen, M Shepherd, A Stride, et al.
Journal of Hepatology
|
July 1, 1992
A survey of cytomegalovirus (CMV) DNA in primary sclerosing cholangitis (PSC) liver tissues using a sensitive polymerase chain reaction (PCR) based assay
W Z Mehal, A T Hattersley, R W Chapman, et al.
Diabetes
|
January 1, 1995
Type II diabetes: clinical aspects of molecular biological studies
R C Turner, A T Hattersley, J T Shaw, et al.
Nature Genetics
|
July 14, 1998
Mutations in the glucokinase gene of the fetus result in reduced birth weight
A T Hattersley, F Beards, E Ballantyne, et al.
Human Mutation
|
September 12, 2000
Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY)
S Ellard, M P Bulman, T M Frayling, et al.
Page
of 18
Search research articles
Search
Showing results (31-40 of 175) with videos related to
Sort By:
Page
of 18
Archives of Disease in Childhood
|
August 24, 2004
Weight differences in Plymouth toddlers compared to the British Growth Reference Population
E Stenhouse, D E Wright, A T Hattersley, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 11, 2009
Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes
O Rubio-Cabezas, E L Edghill, J Argente, et al.
Diabetologia
|
January 12, 2007
The long-term impact on offspring of exposure to hyperglycaemia in utero due to maternal glucokinase gene mutations
R Singh, E R Pearson, P M Clark, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 8, 2009
Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation
G Spyer, K M Macleod, M Shepherd, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
April 25, 2009
A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients
M Shepherd, B Shields, S Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 5, 2002
Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics
K R Owen, M Shepherd, A Stride, et al.
Journal of Hepatology
|
July 1, 1992
A survey of cytomegalovirus (CMV) DNA in primary sclerosing cholangitis (PSC) liver tissues using a sensitive polymerase chain reaction (PCR) based assay
W Z Mehal, A T Hattersley, R W Chapman, et al.
Diabetes
|
January 1, 1995
Type II diabetes: clinical aspects of molecular biological studies
R C Turner, A T Hattersley, J T Shaw, et al.
Nature Genetics
|
July 14, 1998
Mutations in the glucokinase gene of the fetus result in reduced birth weight
A T Hattersley, F Beards, E Ballantyne, et al.
Human Mutation
|
September 12, 2000
Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY)
S Ellard, M P Bulman, T M Frayling, et al.
Page
of 18