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Article

Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation.

Orphanet journal of rare diseases - 4 May 2016

Ju Jun, Hirose Shinichi, Shi Xiu-Yu, Ishii Atsushi, Hu Lin-Yan, Zou Li-Ping

Abstract excerpt

BACKGROUND: Alternating hemiplegia of childhood is an intractable neurological disorder characterized by recurrent episodes of alternating hemiplegia accompanied by other paroxysmal symptoms. Recent research has identified mutations in the ATP1A3 gene as the underlying cause. Adenosine-5'-triphosphate has a vasodilatory effect, can enhance muscle strength and physical performance, and was hypothesized to improve...

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Identifiers

PMID: 27146299
DOI: 10.1186/s13023-016-0438-7
PMCID: PMC4855770

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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