“Alternating” the Diagnosis after 40 Years of Disease: The Thousand Faces of <scp>ATP1A3</scp> Mutation-Reference-Cited by-同舟云学术

“Alternating” the Diagnosis after 40 Years of Disease: The Thousand Faces of ATP1A3 Mutation

Published:2024-01-22 Issue:S2 Volume:11 Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Gallo Silvia¹²^ORCID,Ory‐Magne Fabienne¹^ORCID,Leung Clémence¹,Fabbri Margherita¹³^ORCID,Estublier Bastien⁴,Cheuret Emmanuel⁴,Patat Olivier⁵,Pinheiro Barbosa Raquel¹

Affiliation:

1. Department of Neurology University Hospital of Toulouse Toulouse France

2. Neurology Unit, Department of Translational Medicine University of Piemonte Orientale Novara Italy

3. French Reference Center for MSA, Centre d'Investigation Clinique de Toulouse CIC1436, Department of Neurosciences and Clinical Pharmacology, NS‐Park/FCRIN Network, NeuroToul COEN Center University Hospital of Toulouse, INSERM, University of Toulouse 3 Toulouse France

4. Neuropediatric Department Toulouse‐Purpan University Hospital Toulouse France

5. Department of Medical Genetics Toulouse University Hospital Toulouse France

Publisher

Wiley

Reference8 articles.

1. The Phenotypic Continuum of ATP1A3-Related Disorders

3. Effect of Flunarizine on Alternating Hemiplegia of Childhood in a Patient with the p.E815K Mutation in ATP1A3: A Case Report

4. Alternating hemiplegia

5. Alternating hemiplegia of childhood

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