Role of SCA2 mutations in early‐ and late‐onset dopa‐responsive parkinsonism
2002; Wiley; Volume: 52; Issue: 2 Linguagem: Inglês
10.1002/ana.10270
ISSN1531-8249
AutoresNorman Kock, B. Müller, P. Vieregge, Peter P. Pramstaller, Karen Marder, Giovanni Abbruzzese, Paolo Martinelli, Anthony E. Lang, Helfried Jacobs, Johann Hagenah, Juliette Harris, Helen Meija‐Santana, Stanley Fahn, Katja Hedrich, Martin Kann, Ulrike Gehlken, Biljana Čuljković, E. Schwinger, Zbigniew K. Wszołek, Christine Zühlke, Christine Klein,
Tópico(s)Neurological disorders and treatments
ResumoAnnals of NeurologyVolume 52, Issue 2 p. 257-258 Letters Role of SCA2 mutations in early- and late-onset dopa-responsive parkinsonism Norman Kock MD, Norman Kock MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorBirgitt Müller MD, Birgitt Müller MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorPeter Vieregge MD, Peter Vieregge MD Department of Neurology, Hospital Lippe-Lemgo, Lemgo, GermanySearch for more papers by this authorPeter P. Pramstaller MD, Peter P. Pramstaller MD Department of Neurology, General Regional Hospital Bolzano, Bolzano, ItalySearch for more papers by this authorKaren Marder MD, MPH, Karen Marder MD, MPH Department of Neurology, Columbia University, New York Gertrude H. Sergievsky Center, New York Taub Institute for Research on Alzheimer's Disease and the Aging Brain, New York, NYSearch for more papers by this authorGiovanni Abbruzzese MD, Giovanni Abbruzzese MD Department of Neurological Sciences and Vision, University of Genova, Genova, ItalySearch for more papers by this authorPaolo Martinelli MD, Paolo Martinelli MD Department of Neurological Sciences, University of Bologna, Bologna, ItalySearch for more papers by this authorAnthony E. Lang MD, Anthony E. Lang MD Division of Neurology, Department of Medicine, University of Toronto and Toronto Western Hospital, Toronto, CanadaSearch for more papers by this authorHelfried Jacobs MD, Helfried Jacobs MD Department of Neurology, Hospital Rotenburg/Wümme, Rotenburg, GermanySearch for more papers by this authorJohann Hagenah MD, Johann Hagenah MD Departments of Neurology andSearch for more papers by this authorJuliette Harris MS, PhD, Juliette Harris MS, PhD Department of Neurology, Columbia University, New YorkSearch for more papers by this authorHelen Meija-Santana MS, Helen Meija-Santana MS Department of Neurology, Columbia University, New York Gertrude H. Sergievsky Center, New YorkSearch for more papers by this authorStanley Fahn MD, Stanley Fahn MD Department of Neurology, Columbia University, New YorkSearch for more papers by this authorKatja Hedrich MS, Katja Hedrich MS Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorMartin Kann BS, Martin Kann BS Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorUlrike Gehlken BS, Ulrike Gehlken BS Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorBiljana Culjkovic PhD, Biljana Culjkovic PhD Departments of Neurology and Human Genetics, University of Lübeck, Lübeck Faculty of Biology, Belgrade University, Belgrade, YugoslaviaSearch for more papers by this authorEberhard Schwinger MD, Eberhard Schwinger MD Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorZbigniew K. Wszolek MD, Zbigniew K. Wszolek MD Department of Neurology, Mayo Clinic, Jacksonville, FLSearch for more papers by this authorChristine Zühlke PhD, Christine Zühlke PhD Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorChristine Klein MD, Christine Klein MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this author Norman Kock MD, Norman Kock MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorBirgitt Müller MD, Birgitt Müller MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorPeter Vieregge MD, Peter Vieregge MD Department of Neurology, Hospital Lippe-Lemgo, Lemgo, GermanySearch for more papers by this authorPeter P. Pramstaller MD, Peter P. Pramstaller MD Department of Neurology, General Regional Hospital Bolzano, Bolzano, ItalySearch for more papers by this authorKaren Marder MD, MPH, Karen Marder MD, MPH Department of Neurology, Columbia University, New York Gertrude H. Sergievsky Center, New York Taub Institute for Research on Alzheimer's Disease and the Aging Brain, New York, NYSearch for more papers by this authorGiovanni Abbruzzese MD, Giovanni Abbruzzese MD Department of Neurological Sciences and Vision, University of Genova, Genova, ItalySearch for more papers by this authorPaolo Martinelli MD, Paolo Martinelli MD Department of Neurological Sciences, University of Bologna, Bologna, ItalySearch for more papers by this authorAnthony E. Lang MD, Anthony E. Lang MD Division of Neurology, Department of Medicine, University of Toronto and Toronto Western Hospital, Toronto, CanadaSearch for more papers by this authorHelfried Jacobs MD, Helfried Jacobs MD Department of Neurology, Hospital Rotenburg/Wümme, Rotenburg, GermanySearch for more papers by this authorJohann Hagenah MD, Johann Hagenah MD Departments of Neurology andSearch for more papers by this authorJuliette Harris MS, PhD, Juliette Harris MS, PhD Department of Neurology, Columbia University, New YorkSearch for more papers by this authorHelen Meija-Santana MS, Helen Meija-Santana MS Department of Neurology, Columbia University, New York Gertrude H. Sergievsky Center, New YorkSearch for more papers by this authorStanley Fahn MD, Stanley Fahn MD Department of Neurology, Columbia University, New YorkSearch for more papers by this authorKatja Hedrich MS, Katja Hedrich MS Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorMartin Kann BS, Martin Kann BS Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorUlrike Gehlken BS, Ulrike Gehlken BS Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorBiljana Culjkovic PhD, Biljana Culjkovic PhD Departments of Neurology and Human Genetics, University of Lübeck, Lübeck Faculty of Biology, Belgrade University, Belgrade, YugoslaviaSearch for more papers by this authorEberhard Schwinger MD, Eberhard Schwinger MD Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorZbigniew K. Wszolek MD, Zbigniew K. Wszolek MD Department of Neurology, Mayo Clinic, Jacksonville, FLSearch for more papers by this authorChristine Zühlke PhD, Christine Zühlke PhD Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorChristine Klein MD, Christine Klein MD Departments of Neurology and Human Genetics, University of Lübeck, LübeckSearch for more papers by this author First published: 23 July 2002 https://doi.org/10.1002/ana.10270Citations: 13Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 Shan DE, Soong BW, Sun CM, et al. Spinocerebellar ataxia type 2 presenting as familial levodopa responsive parkinsonism. Ann Neurol 2001; 50: 812-815. 2 Gwinn-Hardy K, Chen JY, Liu H, et al. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology 2000; 55: 800-805. 3 Vaughan JR, Davis MB, Wood NW. Genetics of parkinsonism: a review. Ann Hum Genet 2001; 65: 111-126. 4 Pulst SM, Nechiporuk A, Nechiporuk T, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet 1996; 14: 269-276. 5 Hedrich K, Kann M, Lanthaler AJ, et al. The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism. Hum Mol Genet 2001; 10: 1649-1656. Citing Literature Volume52, Issue2August 2002Pages 257-258 ReferencesRelatedInformation
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