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「"Roeber S "[Author]」の検索結果

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Copathology in Progressive Supranuclear Palsy: Does It Matter?

Validation of the movement disorder society criteria for the diagnosis of 4-repeat tauopathies.

C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy.

How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.

Publisher Correction: ApoE attenuates unresolvable inflammation by complex formation with activated C1q.

ApoE attenuates unresolvable inflammation by complex formation with activated C1q.

DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex.

The USP8 mutational status may predict long-term remission in patients with Cushing's disease.

Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression.

Transient Vestibulopathy in Wallenberg's Syndrome: Pathologic Analysis.

Altered Expression of Growth Associated Protein-43 and Rho Kinase in Human Patients with Parkinson's Disease.

Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.

[A Pair of Siblings with a rare R5H-Mutation in Exon 1 of the MAPT-Gene].

Saccadic Palsy following Cardiac Surgery: Possible Role of Perineuronal Nets.

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

Saccadic palsy following cardiac surgery: a review and new hypothesis.

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

White matter pathology and disconnection in the frontal lobe in CADASIL.

Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.

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