نتایج جستجو برای: wolfram mine
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Wolfram syndrome is a relatively unexplored entity in clinical psychiatry. Historically, the discovery of a specific WFS1 gene had generated huge fanfare regarding specific genetic causations of psychiatric disorders. While the initial enthusiasm has faded now, association of Wolfram syndrome with psychiatric illnesses like schizophrenia, psychosis and suicidal behavior still remain important f...
Wolfram syndrome presenting marked brain MR imaging abnormalities with few neurologic abnormalities.
Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabetes mellitus, optic atrophy, and deafness; DIDMOAD is a commonly accepted anonym for this disorder. We describe a 35-year-old man with Wolfram syndrome, who had marked atrophy of the brain stem, middle cerebellar peduncle, and cerebellum. Despite these MR imaging findings involving the pontocerebellar tra...
EDITOR—Wolfram syndrome (OMIM 222300) is a progressive neurodegenerative disorder characterised by the association of juvenile, non-autoimmune, insulin dependent diabetes mellitus and optic atrophy. The physician D J Wolfram, who reported four cases in 1938, is credited with the first description. With the identification of other clinical features, Wolfram syndrome was also referred to as DIDMO...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed when insulin-dependent diabetes of non-auto-immune origin and optic atrophy are concomitantly present. Wolfram syndrome is also designated by DIDMOAD that stands for its most frequent manifestations: diabetes insipidus, diabetes mellitus, optic atrophy and deafness. With disease progression, pat...
German Ott, Marita Ziepert, Wolfram Klapper, Heike Horn, Monika Szczepanowski, Heinz-Wolfram Bernd, Christoph Thorns, Alfred C. Feller, Dido Lenze, Michael Hummel, Harald Stein, Hans-Konrad Müller-Hermelink, Matthias Frank, Martin-Leo Hansmann, Thomas F. E. Barth, Peter Möller, Sergio Cogliatti, Michael Pfreundschuh, Norbert Schmitz, Lorenz Trümper, Markus Loeffler, Andreas Rosenwald for the DS...
wolfram یا didmoad syndrome یک بیماری نادر ژنتیکی است که همراه با بیماری هایی نظیر دیابت، دیابت بیمزه، آتروفی عصب اپتیک و بعضی اختلالات نورولوژیک دیگر می باشد. بیمار حاضر، دختر 23 ساله ای است که با این تشخیص معرفی می گردد.
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