Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome

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Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome

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2015 nî lūn-bûn

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name

Diabetes mellitus, diabetes in ...... of Wolfram (DIDMOAD) syndrome

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Diabetes mellitus, diabetes in ...... of Wolfram (DIDMOAD) syndrome

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Diabetes mellitus, diabetes in ...... of Wolfram (DIDMOAD) syndrome

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P1476

Diabetes mellitus, diabetes in ...... of Wolfram (DIDMOAD) syndrome

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P2093

Zahra Tavosi

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P2860

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1

Evidence of widespread axonal pathology in Wolfram syndrome.

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

Morbidity and mortality in the Wolfram syndrome.

Urological manifestations of the Wolfram syndrome: observations in 14 patients.

Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study.

Molecular characterization of WFS1 in patients with Wolfram syndrome

Glycemic variability in patients with Wolfram syndrome is lower than in type 1 diabetes.

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132-135

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scholarly article

case report

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10.1016/J.JOCO.2015.11.003

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3-4

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2015-09-01T00:00:00Z

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291013863

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27239592

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4881228

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