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「"Stamelou M "[Author]」の検索結果

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Late-onset cerebellar ataxia: Do not forget Friedreich's.

Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients.

The clinical and genetic heterogeneity of paroxysmal dyskinesias.

From a single nucleotide polymorphism to tau pathology: Appoptosin is the missing link.

Interventions in progressive supranuclear palsy.

The role of cerebellum in patients with late onset cervical/segmental dystonia?--evidence from the clinic.

Multiple system atrophy-mimicking conditions: Diagnostic challenges.

The frontal assessment battery is not useful to discriminate progressive supranuclear palsy from frontotemporal dementias.

Reward Pays the Cost of Noise Reduction in Motor and Cognitive Control.

ADCY5 mutations are another cause of benign hereditary chorea.

What do patients with scans without evidence of dopaminergic deficit (SWEDD) have? New evidence and continuing controversies.

Brain energy metabolism in early MSA-P: A phosphorus and proton magnetic resonance spectroscopy study.

Mutations in HPCA cause autosomal-recessive primary isolated dystonia.

H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?

Atypical parkinsonism: diagnosis and treatment.

The phenotypic spectrum of progressive supranuclear palsy: A retrospective multicenter study of 100 definite cases.

Patients with scans without evidence of dopaminergic deficit: a long-term follow-up study.

The entity of parkinsonism and associated lipomatosis.

Clinical relevance of serum antibodies to extracellular N-methyl-d-aspartate receptor epitopes.

All in the blink of an eye: new insight into cerebellar and brainstem function in DYT1 and DYT6 dystonia.

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