(Q36421763)

14 August 2017

title

High prevalence of abnormal glucose homeostasis secondary to decreased insulin secretion in individuals with hereditary haemochromatosis (English)

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14 August 2017

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McClain DA

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14 August 2017

Abraham D

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14 August 2017

Rogers J

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14 August 2017

Brady R

4

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14 August 2017

Gault P

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Ajioka R

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14 August 2017

Kushner JP

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14 August 2017

language of work or name

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15 March 2006

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14 August 2017

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14 August 2017

volume

49

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14 August 2017

issue

7

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14 August 2017

page(s)

1661-1669

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https://scigraph.springernature.com/pub.10.1007/s00125-006-0200-0

14 August 2017

exact match

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cites work

C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes

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Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study

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Assessing the predictive accuracy of QUICKI as a surrogate index for insulin sensitivity using a calibration model

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Effects of experimental hemosiderosis on pancreatic tissue iron content and structure.

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Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation

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Further evidence for an association between non-insulin-dependent diabetes mellitus and chronic hepatitis C virus infection

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Hepcidin is decreased in TFR2 hemochromatosis

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Method of insulin administration has no effect on insulin sensitivity estimates from the insulin-modified minimal model protocol

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12 December 2020

Prevalence of HFE (hemochromatosis gene) mutations in unselected male patients with type 2 diabetes

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Clinical aspects of diabetes secondary to idiopathic haemochromatosis in French-speaking Belgium

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12 December 2020

Factors affecting glucose tolerance in hereditary hemochromatosis

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The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

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12 December 2020

Quantification of the relationship between insulin sensitivity and beta-cell function in human subjects. Evidence for a hyperbolic function.

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12 December 2020

Hereditary hemochromatosis

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12 December 2020

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12 December 2020

The iron transporter DMT1.

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12 December 2020

Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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12 December 2020

MINMOD Millennium: a computer program to calculate glucose effectiveness and insulin sensitivity from the frequently sampled intravenous glucose tolerance test.

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Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study

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Potential role of increased iron stores in diabetes

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12 December 2020

Insulin resistance-associated hepatic iron overload.

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12 December 2020

Glucose tolerance and beta-cell secretion in patients with thalassaemia major.

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12 December 2020

Relative contribution of iron burden, HFE mutations, and insulin resistance to fibrosis in nonalcoholic fatty liver

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12 December 2020

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

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12 December 2020

Patients with type 2 diabetes have a high frequency of the C282Y mutation of the hemochromatosis gene

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12 December 2020

Clinical characteristics of type 2 diabetes in patients with mutations of HFE

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12 December 2020

Body iron stores in relation to risk of type 2 diabetes in apparently healthy women

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12 December 2020

Oxidative stress, beta-cell apoptosis, and decreased insulin secretory capacity in mouse models of hemochromatosis.

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12 December 2020

Hemochromatosis and iron-overload screening in a racially diverse population.

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Histologic features of the liver in insulin resistance-associated iron overload. A study of 139 patients

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Insulin sensitivity and beta-cell secretion in thalassaemia major with secondary haemochromatosis: assessment by oral glucose tolerance test

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Role of hemochromatosis C282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy

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Large amount of (apo)ferritin in the pancreatic insulin cell and its stimulation by glucose.

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12 December 2020

Clinical features of genetic hemochromatosis in women compared with men.

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12 December 2020

Rapid detection of genetic mutations associated with haemochromatosis

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Body iron stores are associated with serum insulin and blood glucose concentrations. Population study in 1,013 eastern Finnish men.

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The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis.

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12 December 2020

Insulin resistance and hyperinsulinemia in patients with thalassemia major treated by hypertransfusion.

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12 December 2020

Clinical expression and insulin sensitivity in type 2 diabetic patients with heterozygous mutations for haemochromatosis

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12 December 2020

Cross-talk between iron metabolism and diabetes

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12 December 2020

Hereditary haemochromatosis.

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12 December 2020

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

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Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

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12 December 2020

Prevalence of genetic hemochromatosis in a cohort of Italian patients with diabetes mellitus

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12 December 2020

10.1007/S00125-006-0200-0

Identifiers

DOI

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14 August 2017

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