<scp>PSP‐Richardson</scp>'s Syndrome as a Rare Phenotypic Expression of Very Late‐Onset Huntington's Disease: A Case Report-Reference-Cited by-同舟云学术

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PSP‐Richardson's Syndrome as a Rare Phenotypic Expression of Very Late‐Onset Huntington's Disease: A Case Report

Published:2024-01-03 Issue: Volume: Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Prange Stephane¹²³^ORCID,Laurencin Chloé¹^ORCID,Roche Pauline¹,Quadrio Isabelle⁴,Thobois Stéphane¹²³

Affiliation:

1. Hospices Civils de Lyon, Department of Neurology C, Expert Parkinson Center NS‐PARK/FCRIN Pierre Wertheimer Neurological Hospital Bron France

2. Univ Lyon, Marc Jeannerod Cognitive Neuroscience Institute, CNRS, UMR 5229 Bron France

3. Univ Lyon, Faculté de Médecine et de Maïeutique Lyon Sud Charles Mérieux Université Claude Bernard Lyon 1 Oullins France

4. Hospices Civils de Lyon, Neurobiology and Neurogenetics Department of Biochemistry and Molecular Biology Lyon France

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

1. Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities

2. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

3. Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies

4. The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease

5. CAG-repeat length and the age of onset in Huntington disease (HD): A review and validation study of statistical approaches

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