SPG15 : A Rare Correlation with Atypical Juvenile Parkinsonism Responsive to Levodopa-Reference-Cited by-同舟云学术

SPG15 : A Rare Correlation with Atypical Juvenile Parkinsonism Responsive to Levodopa

Published:2020-08-26 Issue:7 Volume:7 Page:842-844
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Araujo Filipe Miranda Milagres¹^ORCID,Junior Wilson Marques²,Tomaselli Pedro José²,Pimentel Ângela V.¹,Macruz Brito Manuelina C.¹,Tumas Vitor¹

Affiliation:

1. Movement Disorders and Behavioral Neurology Section University of São Paulo Ribeirão Preto Brazil

2. Neurogenetics Section, Department of Neurosciences and Behavioral Sciences Ribeirão Preto Medical School Hospital, University of São Paulo (USP) Ribeirão Preto Brazil

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13027

Reference10 articles.

1. Clinical and molecular characterization of hereditary spastic paraplegias: A next-generation sequencing panel approach

2. Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48

3. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms

4. Complicated Hereditary Spastic Paraplegia with Thin Corpus Callosum (HSP‐TCC) and Childhood Onset

5. Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

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4. A Practical Approach to Early-Onset Parkinsonism;Journal of Parkinson's Disease;2022-01-21

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