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Diabetic Medicine : a Journal of the British Diabetic Association
|
June 3, 2008
Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)
S A Eide, H Raeder, S Johansson, et al.
Hepatology (Baltimore, Md.)
|
April 1, 1997
Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes
K E Fladmark, B T Gjertsen, A Molven, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
July 23, 2008
Lack of pancreatic body and tail in HNF1B mutation carriers
I S Haldorsen, M Vesterhus, H Raeder, et al.
Diabetologia
|
April 26, 2008
Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)
J K Hertel, S Johansson, H Raeder, et al.
Clinical Genetics
|
May 29, 2009
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy
T Sandal, L B Laborie, K Brusgaard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
April 23, 2013
Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas
E Tjora, G Wathle, F Erchinger, et al.
Diabetologia
|
April 30, 2013
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
H U Irgens, J Molnes, B B Johansson, et al.
Diabetes Research and Clinical Practice
|
September 22, 2017
The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes
J V Sagen, L Bjørkhaug, B I Haukanes, et al.
The New England Journal of Medicine
|
May 24, 2001
Neonatal diabetes mellitus due to complete glucokinase deficiency
P R Njølstad, O Søvik, A Cuesta-Muñoz, et al.
Molecular Psychiatry
|
December 31, 2003
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder
G Sjøholt, R P Ebstein, R T Lie, et al.
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of 5
Search research articles
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Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 3, 2008
Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)
S A Eide, H Raeder, S Johansson, et al.
Hepatology (Baltimore, Md.)
|
April 1, 1997
Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes
K E Fladmark, B T Gjertsen, A Molven, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
July 23, 2008
Lack of pancreatic body and tail in HNF1B mutation carriers
I S Haldorsen, M Vesterhus, H Raeder, et al.
Diabetologia
|
April 26, 2008
Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)
J K Hertel, S Johansson, H Raeder, et al.
Clinical Genetics
|
May 29, 2009
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy
T Sandal, L B Laborie, K Brusgaard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
April 23, 2013
Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas
E Tjora, G Wathle, F Erchinger, et al.
Diabetologia
|
April 30, 2013
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
H U Irgens, J Molnes, B B Johansson, et al.
Diabetes Research and Clinical Practice
|
September 22, 2017
The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes
J V Sagen, L Bjørkhaug, B I Haukanes, et al.
The New England Journal of Medicine
|
May 24, 2001
Neonatal diabetes mellitus due to complete glucokinase deficiency
P R Njølstad, O Søvik, A Cuesta-Muñoz, et al.
Molecular Psychiatry
|
December 31, 2003
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder
G Sjøholt, R P Ebstein, R T Lie, et al.
Page
of 5