Commentary: Juvenile Dystonia‐Parkinsonism due to DNAJC6 Mutation
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Published in: | Movement disorders clinical practice (Hoboken, N.J.) Vol. 8; no. Suppl 1; pp. S29 - S31 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken, USA
John Wiley & Sons, Inc
01-08-2021
Wiley Subscription Services, Inc |
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Author | Martinez‐Ramirez, Daniel Garza‐Brambila, David Fasano, Alfonso Esparza‐Hernández, Claudia Nallely Ramirez‐Zenteno, Jorge Barsottini, Orlando |
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AuthorAffiliation | 1 Division of General Neurology and Ataxia Unit, Department of Neurology Federal University of São Paulo São Paulo Brazil 3 Centro de Rehabilitacion e Inclusión Infantil Teleton Chihuahua Mexico 4 Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital Toronto Ontario Canada 5 Division of Neurology UHN Toronto Ontario Canada 6 Division of Neurology University of Toronto Toronto Ontario Canada 2 Tecnologico de Monterrey, Escuela de Medicina y Ciencias da la Salud Monterrey Mexico 7 Krembil Brain Institute Toronto Ontario Canada |
AuthorAffiliation_xml | – name: 3 Centro de Rehabilitacion e Inclusión Infantil Teleton Chihuahua Mexico – name: 1 Division of General Neurology and Ataxia Unit, Department of Neurology Federal University of São Paulo São Paulo Brazil – name: 7 Krembil Brain Institute Toronto Ontario Canada – name: 2 Tecnologico de Monterrey, Escuela de Medicina y Ciencias da la Salud Monterrey Mexico – name: 5 Division of Neurology UHN Toronto Ontario Canada – name: 4 Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital Toronto Ontario Canada – name: 6 Division of Neurology University of Toronto Toronto Ontario Canada |
Author_xml | – sequence: 1 givenname: Orlando orcidid: 0000-0002-0107-0831 surname: Barsottini fullname: Barsottini, Orlando email: orlandobarsottini@gmail.com organization: Federal University of São Paulo – sequence: 2 givenname: David orcidid: 0000-0002-1196-7140 surname: Garza‐Brambila fullname: Garza‐Brambila, David organization: Tecnologico de Monterrey, Escuela de Medicina y Ciencias da la Salud – sequence: 3 givenname: Claudia Nallely surname: Esparza‐Hernández fullname: Esparza‐Hernández, Claudia Nallely organization: Tecnologico de Monterrey, Escuela de Medicina y Ciencias da la Salud – sequence: 4 givenname: Jorge orcidid: 0000-0001-5481-6230 surname: Ramirez‐Zenteno fullname: Ramirez‐Zenteno, Jorge organization: Centro de Rehabilitacion e Inclusión Infantil Teleton – sequence: 5 givenname: Daniel surname: Martinez‐Ramirez fullname: Martinez‐Ramirez, Daniel organization: Tecnologico de Monterrey, Escuela de Medicina y Ciencias da la Salud – sequence: 6 givenname: Alfonso orcidid: 0000-0001-5346-0180 surname: Fasano fullname: Fasano, Alfonso organization: Krembil Brain Institute |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34514043$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1002/mds.28063 10.1093/brain/awz345 10.1002/ana.24553 |
ContentType | Journal Article |
Copyright | 2021 International Parkinson and Movement Disorder Society |
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DocumentTitleAlternate | DNAJC6 MUTATION |
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Keywords | dystonia‐parkinsonism syndrome DNAJC6 mutation juvenile parkinsonism |
Language | English |
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Notes | Relevant disclosures and conflicts of interest are listed at the end of this article. SourceType-Other Sources-1 content type line 63 ObjectType-Editorial-2 ObjectType-Commentary-1 |
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PublicationDate | August 2021 |
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PublicationPlace | Hoboken, USA |
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PublicationTitle | Movement disorders clinical practice (Hoboken, N.J.) |
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PublicationYear | 2021 |
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References | 2021; 8 2020; 25 2020; 143 2016; 79 Garza‐Brambila D (e_1_2_4_2_1) 2021; 8 e_1_2_4_3_1 e_1_2_4_5_1 e_1_2_4_4_1 |
References_xml | – volume: 143 start-page: 751 issue: 3 year: 2020 end-page: 770 article-title: Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence publication-title: Brain – volume: 8 start-page: S26 issue: S1 year: 2021 end-page: S28 article-title: Juvenile dystonia‐parkinsonism due to DNAJC6 mutation publication-title: Mov Disord Clin Pract – volume: 25 start-page: 1357 issue: 8 year: 2020 end-page: 1368 article-title: DNAJC6 mutations disrupt dopamine homeostasis in juvenile parkinsonism‐dystonia publication-title: Mov Disord – volume: 79 start-page: 244 year: 2016 end-page: 256 article-title: DNAJC6 mutations associated with early‐onset Parkinson's disease publication-title: Ann Neurol – ident: e_1_2_4_4_1 doi: 10.1002/mds.28063 – ident: e_1_2_4_3_1 doi: 10.1093/brain/awz345 – volume: 8 start-page: S26 issue: 1 year: 2021 ident: e_1_2_4_2_1 article-title: Juvenile dystonia‐parkinsonism due to DNAJC6 mutation publication-title: Mov Disord Clin Pract contributor: fullname: Garza‐Brambila D – ident: e_1_2_4_5_1 doi: 10.1002/ana.24553 |
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SubjectTerms | Brain diseases Case Reports and Commentaries DNAJC6 mutation dystonia‐parkinsonism syndrome juvenile parkinsonism |
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Title | Commentary: Juvenile Dystonia‐Parkinsonism due to DNAJC6 Mutation |
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