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「"Stamelou M "[Author]」の検索結果

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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.

The expanding universe of disorders of the basal ganglia.

Facial tremor in dystonia.

Commentary.

Susceptibility-weighted imaging changes suggesting brain iron accumulation in Huntington's disease: an epiphenomenon which causes diagnostic difficulty.

ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.

The phenotypic spectrum of DYT24 due to ANO3 mutations.

Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.

Psychogenic paroxysmal movement disorders - Clinical features and diagnostic clues.

Ataxia telangiectasia presenting as dopa-responsive cervical dystonia.

Atypical parkinsonism: an update.

[MSA-QoL: disease-specific questionnaire to assess health-related quality of life in multiple system atrophy : Validation of the German translation].

Markedly asymmetric presentation in multiple system atrophy.

Dystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes?

"Atypical" atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-A diagnostic guide.

Familial psychogenic movement disorders.

Tremulous cervical dystonia is likely to be familial: clinical characteristics of a large cohort.

Functional movement disorders are not uncommon in the elderly.

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