The expanding clinical and genetic spectrum of ATP1A3-related disorders-Reference-Cited by-同舟云学术

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The expanding clinical and genetic spectrum of ATP1A3-related disorders

Published:2014-02-12 Issue:11 Volume:82 Page:945-955
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Rosewich H.,Ohlenbusch A.,Huppke P.,Schlotawa L.,Baethmann M.,Carrilho I.,Fiori S.,Lourenco C. M.,Sawyer S.,Steinfeld R.,Gartner J.,Brockmann K.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 102 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Childhood fever and hearing loss associated with CAPOS syndrome;Auris Nasus Larynx;2024-08

2. In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism;Frontiers in Neuroscience;2024-07-31

3. ATP1A3-alternating hemiplegia;Russian neurological journal;2024-03-11

4. Alternating hemiplegia of childhood misdiagnosed as hysteria: a case report;Acta Epileptologica;2024-02-01

5. Dystonia;Movement Disorders Phenomenology;2024

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