Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene)-Reference-Cited by-同舟云学术

Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene)

Published:2001-04 Issue:2 Volume:7 Page:81-88
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Pal P.K,Wszolek Z.K,Kishore A,de la Fuente-Fernandez R,Sossi V,Uitti R.J,Dobko T,Stoessl A.J

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference48 articles.

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2. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21;Wijker;Human Mol Genet,1996

3. Familial parkinsonism: our experience and review;Denson;Parkinson Rel Disord,1995

4. Rapidly progressive autosomal dominant Parkinsonism and dementia with pallido-ponto-nigral degeneration (PPND) and Disinhibition–dementia–parkinsonism–amyotrophy complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22;Wszolek;Parkinson Rel Disord,1997

5. Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration;Wszolek,1993

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