Age‐Related Parkinsonian Signs in Microdeletion 22q11.2-Reference-Cited by-同舟云学术

Age‐Related Parkinsonian Signs in Microdeletion 22q11.2

Published:2020-05-09 Issue:7 Volume:35 Page:1239-1245
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Boot Erik¹²³^ORCID,Mentzel Thierry Q.⁴,Palmer Lisa D.¹,Harten Peter N.³⁴,Marras Connie⁵⁶,Lang Anthony E.⁵⁶,Bassett Anne S.¹⁷⁸⁹^ORCID

Affiliation:

1. The Dalglish Family 22q ClinicUniversity Health Network Toronto Ontario Canada

2. Advisium,'s Heeren Loo Zorggroep Amersfoort The Netherlands

3. Department of Psychiatry & NeuropsychologyMaastricht University Maastricht The Netherlands

4. Innova, Psychiatric Centre GGz Centraal Amersfoort The Netherlands

5. The Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders ClinicToronto Western Hospital and University of Toronto Toronto Ontario Canada

6. Division of Neurology, Department of MedicineUniversity of Toronto Toronto Ontario Canada

7. Clinical Genetics Research Program, and Campbell Family Mental Health Research InstituteCentre for Addiction and Mental Health Toronto Ontario Canada

8. Department of Psychiatry, Division of Cardiology, Department of Medicine, and Toronto General Research InstituteUniversity Health Network Toronto Ontario Canada

9. Department of PsychiatryUniversity of Toronto Toronto Ontario Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28080

Reference28 articles.

1. Association Between Early-Onset Parkinson Disease and 22q11.2 Deletion Syndrome

2. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

3. Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2

4. 22q11.2 Deletion Syndrome-Associated Parkinson's Disease

5. Hyposmia, symptoms of rapid eye movement sleep behavior disorder, and parkinsonian motor signs suggest prodromal neurodegeneration in 22q11 deletion syndrome

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1. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

2. Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults;European Journal of Human Genetics;2022-08-25

3. Mental health in adults with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022