PINK1 mutation in Taiwanese early-onset parkinsonism-Reference-Cited by-同舟云学术

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PINK1 mutation in Taiwanese early-onset parkinsonism

Published:2007-10 Issue:10 Volume:254 Page:1347-1355
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Weng Yi-Hsin,Chou Yah-Huei Wu,Wu Wen-Shiang,Lin Kun-Ju,Chang Hsiu-Chen,Yen Tzu-Chen,Chen Rou-Shayn,Wey Shiaw-Pyng,Lu Chin-Song

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-007-0534-7.pdf

Reference33 articles.

1. Tanner CM, Ottman R, Goldman SM, Ellenberg J, Chan P, Mayeux R, Langston JW (1999) Parkinson Disease in Twins: An Etiologic Study. JAMA 281:341-46

2. Bonifati V, Rizzu P, Squitieri F, Krieger E, Vanacore N, van Swieten JC, Brice A, van Duijn CM, Oostra B, Meco G, Heutink P (2003) DJ-1(PARK7), a novel gene for autosomal recessive, early onset parkinsonism. Neurol Sci 24:159-60

3. Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL (1997) Mutation in the alpha-Synuclein Gene Identified in Families with Parkinson's Disease. Science 276:2045-047

4. Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, van der Brug M, Lopez de Munain A, Aparicio S, Gil AM, Khan N, Johnson J, Martinez JR, Nicholl D, Carrera IM, Pena AS, de Silva R, Lees A, Marti-Masso JF, Perez-Tur J, Wood NW, Singleton AB. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 44:595-00

5. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N (1998) Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:605-08

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1. Dopaminergic molecular imaging in familial and idiopathic Parkinson's disease;Neuroimaging in Parkinson�s Disease and Related Disorders;2023

2. Disruption of Mitochondrial Homeostasis: The Role of PINK1 in Parkinson’s Disease;Cells;2021-11-04

3. The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1;Neurobiology of Aging;2021-01

4. Novel ATP13A2 and PINK1 variants identified in Chinese patients with Parkinson’s disease by whole-exome sequencing;Neuroscience Letters;2020-08

5. Genetic perspective on the synergistic connection between vesicular transport, lysosomal and mitochondrial pathways associated with Parkinson’s disease pathogenesis;Acta Neuropathologica Communications;2020-05-06

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