Neuroimaging study in autosomal dominant cerebellar ataxia, deafness, and narcolepsy.

Melberg, A; Dahl, N; Hetta, J; Valind, S; Nennesmo, I; Lundberg, P O; Raininko, R

Melberg, A; Dahl, N; Hetta, J; Valind, S; Nennesmo, I; Lundberg, P O; Raininko, R.

Affiliation

Melberg A; Department of Neuroscience, Uppsala University Hospital, Sweden. atle.melberg@neurologi.uu.se

Neurology ; 53(9): 2190-2, 1999 Dec 10.

Article in En | MEDLINE | ID: mdl-10599806

Subject(s)

Chromosome Aberrations/genetics; Deafness/genetics; Genes, Dominant/genetics; Narcolepsy/genetics; Spinocerebellar Degenerations/genetics; Adolescent; Adult; Atrophy; Brain/pathology; Chromosome Disorders; DNA Mutational Analysis; Deafness/diagnosis; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Narcolepsy/diagnosis; Pedigree; Spinocerebellar Degenerations/diagnosis; Tomography, X-Ray Computed

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Collection: 01-internacional Database: MEDLINE Main subject: Spinocerebellar Degenerations / Chromosome Aberrations / Deafness / Genes, Dominant / Narcolepsy Type of study: Diagnostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 1999 Document type: Article

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