Three families with Perry syndrome from distinct parts of the world-Reference-Cited by-同舟云学术

Three families with Perry syndrome from distinct parts of the world

Published:2014-08 Issue:8 Volume:20 Page:884-888
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Tacik Pawel,Fiesel Fabienne C.,Fujioka Shinsuke^ORCID,Ross Owen A.,Pretelt Felipe,Castañeda Cardona Camilo,Kidd Alexa,Hlavac Michael,Raizis Anthony,Okun Michael S.,Traynor Sharleen,Strongosky Audrey J.,Springer Wolfdieter,Wszolek Zbigniew K.

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference13 articles.

1. Hereditary mental depression and Parkinsonism with taurine deficiency;Perry;Arch Neurol,1975

2. Elucidating the genetics and pathology of Perry syndrome;Wider;J Neurol Sci,2010

3. Perry syndrome: a disorder to consider in the differential diagnosis of Parkinsonism;Aji;J Neurol Sci,2013

4. DCTN1 mutations in Perry syndrome;Farrer;Nat Genet,2009

5. Latin America's first case of Perry syndrome and a new treatment option for respiratory insufficiency;Pretelt;J Neurol,2014

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1. First family with Perry syndrome from Mexico;Biomedical Reports;2024-06-19

2. Wild-Type DCTN1 Suppresses the Aggregation of DCTN1 Mutants Associated with Perry Disease;Biological and Pharmaceutical Bulletin;2024-01-24

3. Perry Disease: Bench to Bedside Circulation and a Team Approach;Biomedicines;2024-01-05

4. Frequency of Hereditary and GBA1‐Related Parkinsonism in Latin America: A Systematic Review and Meta‐Analysis;Movement Disorders;2023-11-03

5. Perry syndrome with a novel mutation and a rare presentation: First report from India;Annals of Indian Academy of Neurology;2022