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Scholar Results 1 - 10 of about 101 related to Ræder: Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations.... (0.11 sec) 

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in …

- shouxi.net
H Ræder, IS Haldorsen, L Ersland, R Grüner, T … - Diabetes, 2007 - Am Diabetes Assoc
Both pancreatic volume reduction and lipomatosis have been observed in subjects
with diabetes. The underlying molecular and pathological mechanisms are,
however, poorly known, and it has been speculated that both features are ...
Cited by 20 - Related articles - BL Direct - All 6 versions

Pancreatic exocrine dysfunction in maturity-onset diabetes of the young type 3

- Free from Publisher
M Vesterhus, H Ræder, S Johansson, A Molven … - Diabetes Care, 2008 - Am Diabetes Assoc
RESULTS—We found a prevalence of fecal elastase deficiency of 12.7% in adult
patients with MODY3, compared with 18.6% in patients with type 1 diabetes and
3.8% in nondiabetic control subjects. The six patients with MODY3 with ...
Cited by 14 - Related articles - BL Direct - All 7 versions

Lack of pancreatic body and tail in HNF1B mutation carriers


IS Haldorsen, M Vesterhus, H Raeder, DK … - Diabetic Medicine, 2008 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ...
Cited by 10 - Related articles - All 4 versions

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine …


H Ræder, S Johansson, PI Holm, IS Haldorsen, … - Nature genetics, 2005 - nature.com
Cited by 67 - Related articles - BL Direct - All 7 versions

Pancreatic fat content and β-cell function in men with and without type 2 diabetes

- diabetesjournals.org
ME Tushuizen, MC Bunck, PJ Pouwels, S … - Diabetes Care, 2007 - Am Diabetes Assoc
RESULTS—Patients versus control subjects had higher A1C, fasting plasma
glucose, and insulin and triglyceride levels and lower HDL cholesterol, but
similar waist circumference. Median (interquartile range) pancreatic fat ...
Cited by 17 - Related articles - BL Direct - All 5 versions

Obesity and fat quantification in lean tissues using three-point Dixon MR imaging


A Kovanlikaya, SD Mittelman, A Ward, ME … - Pediatric radiology, 2005 - Springer
Worldwide, obesity has reached epidemic proportions. More than 30% of children
in the United States are overweight or obese, and there is no evidence that the
rise in obesity incidence will plateau or decline in the coming years [1, ...
Cited by 20 - Related articles - All 4 versions

[CITATION] Effect of common polymorphisms in the HNF4a promoter on type 2 diabetes susceptibility in …


M Vaxillaire, C Dina, S Lobbens, A Dechaume … - Diabetologia, 2005
Cited by 4 - Related articles

Pancreas volumes in humans from birth to age one hundred taking into account sex, obesity …


Y Saisho, AE Butler, JJ Meier, T Monchamp, M … - Clinical Anatomy (New York, Ny), 2007 - pubmedcentral.nih.gov
Our aims were (1) by computed tomography (CT) to establish a population database
for pancreas volume (parenchyma and fat) from birth to age 100 years, (2) in
adults, to establish the impact of gender, obesity, and the presence or ...
Cited by 14 - Related articles - BL Direct - All 5 versions

Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative …


E Domenech, M Gomez-Zaera, V Nunes - Pediatric endocrinology reviews: PER, 2006 - ncbi.nlm.nih.gov
Wolfram syndrome (WS, OMIM 22233), is a rare, autosomal recessive, and
neurodegenerative disease. The syndrome is also known as DIDMOAD, the acronym
for diabetes insipidus diabetes mellitus, optic atrophy and deafness, which ...
Cited by 16 - Related articles - BL Direct

A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of …


L Liu, H Furuta, A Minami, T Zheng, W Jia, K … - Molecular and Cellular Biochemistry, 2007 - Springer
Abstract Objectives During examining the prevalence of mutations in
NeuroD1/BETA2 gene in Chinese early-onset type 2 diabetic probands, a novel
missense mutation, Ser159Pro in a potential MODY family was identified. To ...
Cited by 7 - Related articles - BL Direct - All 4 versions


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