منابع مشابه
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...
متن کاملسندرم 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.
متن کاملWolfram Hörz 1944–2005
Fields of research are frequently cultivated by a few scientific entrepreneurs whose vision and drive inspire the rest of us. The analysis of chroma-tin structure and function has profited immensely from leaders such as Wolf-ram Hörz. The yeast PHO5 promoter model developed by Wolfram Hörz has become a paradigm for dissecting the events underlying promoter-specific chro-matin opening in respons...
متن کاملWolfram F . Richter
The working papers published in the Series constitute work in progress circulated to stimulate discussion and critical comments. Views expressed represent exclusively the authors' own opinions and do not necessarily reflect those of the editors. Die Deutsche Nationalbibliothek verzeichnet diese Publikation in der Deutschen Nationalbibliografie; detaillierte bibliografische Daten sind im Interne...
متن کاملThe 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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ژورنال
عنوان ژورنال: Journal of Applied Crystallography
سال: 2002
ISSN: 0021-8898
DOI: 10.1107/s0021889801019811