Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

Author:

Viollet Louis,Glusman Gustavo,Murphy Kelley J.,Newcomb Tara M.,Reyna Sandra P.,Sweney Matthew,Nelson Benjamin,Andermann Frederick,Andermann Eva,Acsadi Gyula,Barbano Richard L.,Brown Candida,Brunkow Mary E.,Chugani Harry T.,Cheyette Sarah R.,Collins Abigail,DeBrosse Suzanne D.,Galas David,Friedman Jennifer,Hood Lee,Huff Chad,Jorde Lynn B.,King Mary D.,LaSalle Bernie,Leventer Richard J.,Lewelt Aga J.,Massart Mylynda B.,Mérida Mario R.,Ptáček Louis J.,Roach Jared C.,Rust Robert S.,Renault Francis,Sanger Terry D.,Sotero de Menezes Marcio A.,Tennyson Rachel,Uldall Peter,Zhang Yue,Zupanc Mary,Xin Winnie,Silver Kenneth,Swoboda Kathryn J.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference55 articles.

1. Alternating hemiplegia in childhood: a report of eight patients with complicated migraine beginning in infancy;S Verret;Pediatrics,1971

2. Alternating hemiplegia of childhood;M Bourgeois;J Pediatr,1993

3. A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiological investigations;MA Mikati;Neurology,1992

4. Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait;E Kanavakis;Dev Med Child Neurol,2003

5. A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood;MT Bassi;J Med Genet,2004

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