Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2). - Wikidata - awgldk - TriplyDB

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

http://www.wikidata.org/entity/Q30938617

about

Parkinson's disease: from monogenic forms to genetic susceptibility factors Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes The genetics and neuropathology of Parkinson's disease Genetics of Parkinson's disease - a clinical perspective Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review Parkinsonism in spinocerebellar ataxia Repetitive finger movement performance differs among Parkinson's disease, Progressive Supranuclear Palsy, and spinocerebellar ataxia.Dissociated fear and spatial learning in mice with deficiency of ataxin-2 Ataxin-2 repeat-length variation and neurodegeneration Clinical analysis of adult-onset spinocerebellar ataxias in Thailand.Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2.Cervical dystonia in spinocerebellar ataxia type 2: clinical and polymyographic findings Coexistence of Huntington's disease and amyotrophic lateral sclerosis: a clinicopathologic study.Roles of trinucleotide-repeat RNA in neurological disease and degeneration.An autopsy case of an aged patient with spinocerebellar ataxia type 2.Milestones in neuroimaging.Vertical supranuclear gaze palsy in Niemann-Pick type C disease.Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives.Advances in the genetics of Parkinson disease.Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology.Spinocerebellar ataxia: relationship between phenotype and genotype - a review.The Multiple Faces of Spinocerebellar Ataxia type 2.C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism.Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family.FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion

P2860

Q22242870-FD97E68D-D815-439F-9F4E-31A948F8E0E2 Q24296835-7912D51C-87E2-461B-B0B4-F0854325E8F5 Q26859945-84F80C20-A952-49F2-BEA5-600AAAB1DD4A Q27022109-E915544C-71AB-4AF5-BBF2-1CFEA35519F3 Q28076174-A7820491-D78F-422D-9631-BF335CC12A16 Q28080641-BD4B2BEA-4FFA-49F2-9CDA-3224E28630C3 Q30393518-A3422067-65BA-4756-96D6-9DEAF2948726 Q33484172-7F9D57F5-6211-4EE8-BF6E-0C4043D89A9D Q35119694-F89A5561-D1AC-4025-99DC-941F41735333 Q35141117-3FA16B27-9C0A-4692-8C24-B0C1289B42CB Q35863545-2947369B-5801-4BC7-839D-B6F6C8AFDE13 Q36227397-70B7F623-1AD1-4DFE-8B7D-D50DE4F68475 Q36534978-EA714F17-7E63-44C8-AB20-9D4433727406 Q37732635-FBB5920A-4E07-45E3-B2B3-7DE7124CE4BC Q37816490-12BF637E-C850-478A-8EE3-0367B0CDDD28 Q37882576-197FC543-6B3F-4020-A46A-6D95C2661B95 Q38027335-FC4AAF61-035C-4B7F-BC3F-048C4920692A Q38045212-7CF958D2-CC8C-45D1-8304-1ED190311829 Q38121773-02B8C0EB-B6E4-442E-B45F-815CBFB69F33 Q38412906-4A510638-F627-4B51-A2FF-7E8503133786 Q38843338-D8046C12-151C-4407-AA17-FF468DEA2676 Q41510206-CB8BE8E1-3C58-4D0A-A063-35EDECD3032F Q48706455-A1620A79-31CA-4473-8AF3-4BC40323DD66 Q50265751-F4E0D0C6-64A1-445E-B57F-D40495659D32 Q57921365-479D3FAE-E558-4C84-B555-6E56E24A5D63

P2860

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

http://www.wikidata.org/entity/Q30938617

description

2004 nî lūn-bûn

@nan

2004 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2004年の論文

@ja

2004年論文

@yue

2004年論文

@zh-hant

2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

@zh-tw

2004年论文

@wuu

name

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@ast

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@en

type

label

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@ast

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@en

prefLabel

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@ast

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@en

P1433

Q30938617-005A2AA5-D9A7-4A4E-A7C5-C5DAC0F93332

P1476

Q30938617-3008C4E4-F0E7-4878-A0FE-B134DE57E8BF

P2093

Q30938617-16522A7C-0495-4F5D-9747-DEC2D98D0487

Q30938617-80DA7AD4-CDCE-44BE-BBED-F2DB09A64DAA

Q30938617-82068DAF-AC2E-4D2A-8446-5591B40AF7C5

Q30938617-85F21D08-07EF-4000-B33A-62664E35E14F

Q30938617-913D3062-CFA1-47D6-9A91-F7573E46ECFE

Q30938617-92C362E1-418E-4E12-BB8B-6E3D762B86DC

Q30938617-99EFD42A-A922-47F2-B63A-A74760971C6F

Q30938617-9DD349E3-6EB6-4427-BD62-B969775571D5

Q30938617-A3562700-75F1-4A06-8E68-B30533441998

Q30938617-DC98D06D-A75D-4685-AB20-20DCDE32E121

P2860

Q30938617-0A8D2774-C80B-4B6B-A49E-C215F8D72816

Q30938617-C18595F0-03B4-4F0A-AC39-02427CF09D37

Q30938617-F0C45426-2272-4E2B-8EF8-27BB9B9ECA38

P304

Q30938617-78D2E2C0-E828-42E3-B46A-FC399AA8B3D7

P31

Q30938617-03388146-BD44-4C7C-AC09-68AA4AF3CC38

P356

Q30938617-9C96DE7C-8668-4743-8016-2DB20D322F59

P407

Q30938617-A6257277-52B4-46A9-B483-AA77493D07F3

P433

Q30938617-A98C2015-6E96-4F41-AA63-CF8FDE5B7B0A

P478

Q30938617-4D45F0AE-B723-4067-B800-E1969381309A

P50

Q30938617-114BC631-EBA0-4468-B4DB-E415419AA4A4

Q30938617-19DF890B-802E-4034-BFDD-28E0D9A960E4

Q30938617-6B84D5F1-2D91-43B1-84CF-408462698964

Q30938617-7F688D66-D76D-4A43-BA8D-8DC0BCDD0F87

Q30938617-89D6D82B-945B-40E0-990A-4B6749E3C894

Q30938617-93A4A50C-450E-43ED-9F46-671A6ECDE394

Q30938617-9D05D0DC-61DB-4BDC-B160-1C28E788E1A7

Q30938617-B97FFE3D-8DC7-4866-9218-080E0E1B0627

Q30938617-F97F21B5-48C9-40BE-9F9D-7F42E82824F4

P577

Q30938617-70F8567C-9DC0-4ABA-8661-7D32138303F5

P698

Q30938617-6C9FE7B8-3DA8-4DDB-B7F7-61AE54CC58D4

P921

Q30938617-63AC04EB-E4C9-4853-8B06-EFBA679FA814

Q30938617-98AFBAF4-EEE5-4864-AB79-7CD5ED6F43F6

P356

P1433

Movement Disorders

P1476

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

@en

P2093

Andrew A Singleton

http://www.w3.org/2001/XMLSchema#string

Haydeh Payami

http://www.w3.org/2001/XMLSchema#string

Jamel Bower

http://www.w3.org/2001/XMLSchema#string

Mary L Klimek

http://www.w3.org/2001/XMLSchema#string

Melissa Hanson

http://www.w3.org/2001/XMLSchema#string

Oksana Suchowersky

http://www.w3.org/2001/XMLSchema#string

Raul de la Fuente-Fernandez

http://www.w3.org/2001/XMLSchema#string

Ryan J Utti

http://www.w3.org/2001/XMLSchema#string

Sarah Furtado

http://www.w3.org/2001/XMLSchema#string

Thomas D Bird

http://www.w3.org/2001/XMLSchema#string

P2860

Late-onset SCA2: 33 CAG repeats are sufficient to cause disease.

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.

SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.

P304

622-629

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/MDS.20074

http://www.w3.org/2001/XMLSchema#string

P407

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

19

http://www.w3.org/2001/XMLSchema#string

P50

Matthew J. Farrer

Paul J. Lockhart

Donald Brian Calne

John Anthony Hardy

Zbigniew K Wszolek

Amanda Singleton

P577

2004-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

15197699

http://www.w3.org/2001/XMLSchema#string

P921

Parkinson's disease