Fatal familial insomnia: Clinical features and early identification. - Wikidata - awgldk - TriplyDB

Fatal familial insomnia: Clinical features and early identification.

Fatal familial insomnia: Clinical features and early identification.

http://www.wikidata.org/entity/Q48439556

about

A proposal of new diagnostic pathway for fatal familial insomnia Characteristic CSF prion seeding efficiency in humans with prion diseases Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.Requirements for mutant and wild-type prion protein misfolding in vitro.Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.Clinical, histopathological and genetic studies in a case of fatal familial insomnia with review of the literature Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.Neuropathology of sleep disorders: a review.Hereditary Human Prion Diseases: an Update.Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Neuroimaging in human prion disease: Searching in the mist.Clinical findings and diagnosis in genetic prion diseases in Germany.An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia.Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus.Identification of new molecular alterations in fatal familial insomnia.Metabolic patterns in prion diseases: an FDG PET voxel-based analysis.Neuroimaging in Dementia.

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P2860

Fatal familial insomnia: Clinical features and early identification.

http://www.wikidata.org/entity/Q48439556

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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name

Fatal familial insomnia: Clinical features and early identification.

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Fatal familial insomnia: Clinical features and early identification.

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type

label

Fatal familial insomnia: Clinical features and early identification.

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Fatal familial insomnia: Clinical features and early identification.

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prefLabel

Fatal familial insomnia: Clinical features and early identification.

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Fatal familial insomnia: Clinical features and early identification.

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Annals of Neurology

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Fatal familial insomnia: Clinical features and early identification.

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Anna Krasnianski

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Bettina Meissner

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Daniela Varges

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Haus A Kretzschmar

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Inga Zerr

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Mario Bartl

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Pascual J Sanchez Juan

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Ulf Schulze-Sturm

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Uta Heinemann

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Walter J Schulz-Schaeffer

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P2860

Fatal familial insomnia: clinical and pathologic study of five new cases.

The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.

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658-661

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scholarly article

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10.1002/ANA.21358

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5

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63

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2008-05-01T00:00:00Z

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5491200

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18360821

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