Neurology

Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging.

Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging.

Evidence of genetic heterogeneity among the nondystrophic myotonias.

Evidence of genetic heterogeneity among the nondystrophic myotonias.

Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.

Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.

Linkage of atypical myotonia congenita to a sodium channel locus.

Linkage of atypical myotonia congenita to a sodium channel locus.

Glucose and infarct size.

Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity.

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