Wolfram Tantalum and Wolfram Niobium Oxides of the MnO3n-2(ReO3) Series.

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Wolfram syndrome.

Wolfram syndrome is a rare neurodegenerative and genetic disorder, which should be suspected in patients with young onset non-immune insulin dependent diabetes mellitus and optic atrophy. Patients are most likely to develop diabetes insipidus, deafness, urinary tract, and neurological abnormalities. 60% of the people with Wolfram syndrome die at age 35, usually due to central respiratory center...

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The Wolfram or DIDMOAD syndrome

Seven patients with a rare syndrome of diabetes insipidus (DI), diabetes mellitus (DM), optic atrophy (OA), neurosensory deafness (D), atony of the urinary tract, and other abnormalities (Wolfram or DIDMOAD syndrome) are reported. Of the seven patients, three siblings were followed up for 10-17 years. All seven patients had diabetes mellitus and optic atrophy; six had diabetes insipidus; and in...

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Phenotype-genotype correlations in a series of wolfram syndrome families.

OBJECTIVE Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the development of type 1 diabetes in association with progressive optic atrophy. The genetic basis of this disease has been shown to be due to mutations in the WFS1 gene. The WFS1 gene encodes a novel transmembrane protein called wolframin, which recent evidence suggests may serve as a novel endoplasm...

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سندرم Wolfram

Wolfram (DÏDMÔÂD) Synd usually presents with diabetes mellitus & following that optic atrophy usually happens. Ïn this report we present a case about 23 years old age that has presented with diabetes mellitus since age of 9 Y/Ô.

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Wolfram Hörz 1944–2005

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ژورنال

عنوان ژورنال: Acta Chemica Scandinavica

سال: 1965

ISSN: 0904-213X

DOI: 10.3891/acta.chem.scand.19-2010