Literature DB >> 8505637

Familial progressive supranuclear palsy.

J Brown1, P Lantos, M Stratton, P Roques, M Rossor.   

Abstract

A progressive extrapyramidal syndrome and dementia occurred in three members of one family. The age of onset was in the seventh decade and the affected individuals showed many of the clinical features of progressive supranuclear palsy (PSP). Necropsy of one individual revealed the neuropathological features of PSP. We propose that this family has a familial form of PSP and review the evidence in the literature that a familial form exists.

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Year:  1993        PMID: 8505637      PMCID: PMC1015003          DOI: 10.1136/jnnp.56.5.473

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  22 in total

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  13 in total

Review 1.  Progressive supranuclear palsy.

Authors:  H U Rehman
Journal:  Postgrad Med J       Date:  2000-06       Impact factor: 2.401

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Review 3.  Clinical aspects of familial forms of frontotemporal dementia associated with parkinsonism.

Authors:  Shinsuke Fujioka; Zbigniew K Wszolek
Journal:  J Mol Neurosci       Date:  2011-06-08       Impact factor: 3.444

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Journal:  Drugs Aging       Date:  2001       Impact factor: 3.923

5.  Psychogenic axial myoclonus: report on two cases.

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Journal:  Neurol Sci       Date:  2010-02-05       Impact factor: 3.307

6.  Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.

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8.  Characterization of dopaminergic dysfunction in familial progressive supranuclear palsy: an 18F-dopa PET study.

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9.  Parkinsonism and tremor disorders. A clinical approach.

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Review 10.  Genetics of Progressive Supranuclear Palsy.

Authors:  Sun Young Im; Young Eun Kim; Yun Joong Kim
Journal:  J Mov Disord       Date:  2015-09-10
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