Perry syndrome: A disorder to consider in the differential diagnosis of Parkinsonism
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference18 articles.
1. Hereditary mental depression and Parkinsonism with taurine deficiency;Perry;Arch Neurol,1975
2. Rapidly progressive familial Parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome) — a literature review;Wider;Parkinsonism Relat Disord,2008
3. DCTN1 mutations in Perry syndrome;Farrer;Nat Genet,2009
4. Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioural syndrome, vertical gaze palsy, and respiratory failure;Newsway;Mov Disord,2010
5. Autonomic failures in Perry syndrome with DCTN1 mutation;Ohshima;Parkinsonism Relat Disord,2010
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1. Perry disease in an Argentine family due to the DCTN1 p.G67D variant;Parkinsonism & Related Disorders;2022-04
2. Perry Disease: Concept of a New Disease and Clinical Diagnostic Criteria;Journal of Movement Disorders;2021-01-31
3. Cognitive and behavioral profile of Perry syndrome in two families;Parkinsonism & Related Disorders;2020-08
4. Perry disease: recent advances and perspectives;Expert Opinion on Orphan Drugs;2019-05-04
5. Diagnosis (2): Disorders Causing Dementia and Cognitive Impairment;Dementia in Clinical Practice: A Neurological Perspective;2018
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