Sage Journals: Discover world-class research

Retricted access

Review article

First published 2025-10

Unusual Phenotypic Variability in Paroxysmal Dystonia Associated with Rare ATP1A3 Mutation: A Case Report and Review

Martyna A. Czylok, Milena Prokopiuk, Katarzyna Meller [...]

Journal of Child Neurology

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Research article

First published 2021-04

Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool,Atp1a3 Mashl/+,Mouse Model of Alternating Hemiplegia of Childhood

Arsen S. Hunanyan, Boris Kantor, Ram S. Puranam [...]

Human Gene Therapy

Open access

Research article

First published 2025

The involvement of spinal lncRNA RT1-CE10 in chronic functional visceral pain

Ying Tang, Zihan Liu, Xianhe Wu [...]

Molecular Pain

Open access

Research article

First published 2024

A novel mutation in the ATP1A2 gene associated with a sporadic hemiplegic migraine and multiple supraventricular arrhythmias: A case report

Sarvnaz Shalchian Tehran, Pierre Maquet

Cephalalgia Reports

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Research article

First published 2014-2

A Wide Clinical Phenotype Spectrum in Patients With ATP1A2 Mutations

Bashaer Al-Bulushi, Amal Al-Hashem, Brahim Tabarki

Journal of Child Neurology

Free access

Research article

First published 2008-9

Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients

LL Thomsen, E Oestergaard, A Bjornsson [...]

Cephalalgia

Free access

Research article

First published 2006-3

A Novel ATP1A2 Mutation in a Family with FHM Type II

F Pierelli, GS Grieco, F Pauri [...]

Cephalalgia

Free access

Brief report

First published 2014-1

A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy

Cinzia Costa, Paolo Prontera, Paola Sarchielli [...]

Cephalalgia

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Research article

First published 2015-11

CAOS—Episodic Cerebellar Ataxia,Areflexia,Optic Atrophy,and Sensorineural Hearing Loss

Gali Heimer, Yair Sadaka, Lori Israelian [...]

Journal of Child Neurology

Free access

Brief report

First published 2008-7

Severe Attacks of Familial Hemiplegic Migraine,Childhood Epilepsy and ATP1A2 Mutation

A Lebas, L Guyant-Maréchal, D Hannequin [...]

Cephalalgia

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