Literature DB >> 9726605

Hereditary haemochromatosis mutations (HFE) in patients with Type II diabetes mellitus.

J Braun, H Donner, K Plock, H Rau, K H Usadel, K Badenhoop.   

Abstract

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Year:  1998        PMID： 9726605     DOI： 10.1007/s001250051019

Source DB:  PubMed          Journal:  Diabetologia        ISSN： 0012-186X            Impact factor:   10.122


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  4 in total

1.  Diabetes and HFE mutations: cause or coincidence?

Authors:  Linda E Pinsky; Giuseppina Imperatore; Wylie Burke
Journal:  West J Med       Date:  2002-03

2.  High prevalence of abnormal glucose homeostasis secondary to decreased insulin secretion in individuals with hereditary haemochromatosis.

Authors:  D A McClain; D Abraham; J Rogers; R Brady; P Gault; R Ajioka; J P Kushner
Journal:  Diabetologia       Date:  2006-03-15       Impact factor: 10.122

3.  The HFE gene is associated to an earlier age of onset and to the presence of diabetic nephropathy in diabetes mellitus type 2.

Authors:  Rafael Oliva; Anna Novials; Mayka Sánchez; Marga Villa; Mercedes Ingelmo; Mónica Recasens; Carlos Ascaso; Miquel Bruguera; Ramón Gomis
Journal:  Endocrine       Date:  2004-07       Impact factor: 3.633

4.  The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic.

Authors:  Kathleen M Heath; Jacob H Axton; John M McCullough; Nathan Harris
Journal:  Am J Phys Anthropol       Date:  2016-01-22       Impact factor: 2.868
  4 in total

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