Fifty years of progressive supranuclear palsy. - Wikidata - wikimedia - TriplyDB

Fifty years of progressive supranuclear palsy.

Fifty years of progressive supranuclear palsy.

http://www.wikidata.org/entity/Q38135221

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Disrupted resting-state functional connectivity in progressive supranuclear palsy.MR parkinsonism index predicts vertical supranuclear gaze palsy in patients with PSP-parkinsonism The differentiation of progressive supranuclear palsy.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Neuropathologic features of suicide victims who presented with acute poststroke depression: significance of association with neurodegenerative disorders.La belle indifférence revisited: a case report on progressive supranuclear palsy misdiagnosed as conversion disorder.Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series.MRI gray and white matter measures in progressive supranuclear palsy and corticobasal syndrome.The association of aphasia and right-sided motor impairment in corticobasal syndrome.Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes.Neuroimaging correlates of blinking abnormalities in patients with progressive supranuclear palsy.Microtubule defects in mesenchymal stromal cells distinguish patients with Progressive Supranuclear Palsy.Neuropsychiatric disturbances in atypical parkinsonian disorders

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Fifty years of progressive supranuclear palsy.

http://www.wikidata.org/entity/Q38135221

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artikel ilmiah

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Fifty years of progressive supranuclear palsy.

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Fifty years of progressive supranuclear palsy.

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Fifty years of progressive supranuclear palsy.

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JNNP-2013-305740

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Journal of Neurology, Neurosurgery and Psychiatry

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Fifty years of progressive supranuclear palsy.

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Thomas H Bak

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P2860

Hypokinesia without decrement distinguishes progressive supranuclear palsy from Parkinson's disease

Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study

Tauopathies: classification and clinical update on neurodegenerative diseases associated with microtubule-associated protein tau

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

Prevalence of Parkinson's disease in Northwestern Italy: comparison of tracer methodology and clinical ascertainment of cases.

Donepezil in the treatment of progressive supranuclear palsy.

Accuracy of clinical diagnosis of progressive supranuclear palsy.

Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy.

Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria.

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938-944

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scholarly article

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10.1136/JNNP-2013-305740

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8

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Alfredo Berardelli

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2013-09-06T00:00:00Z

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