Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

Author:

Panagiotakaki Eleni, ,De Grandis Elisa,Stagnaro Michela,Heinzen Erin L.,Fons Carmen,Sisodiya Sanjay,de Vries Boukje,Goubau Christophe,Weckhuysen Sarah,Kemlink David,Scheffer Ingrid,Lesca Gaëtan,Rabilloud Muriel,Klich Amna,Ramirez-Camacho Alia,Ulate-Campos Adriana,Campistol Jaume,Giannotta Melania,Moutard Marie-Laure,Doummar Diane,Hubsch-Bonneaud Cecile,Jaffer Fatima,Cross Helen,Gurrieri Fiorella,Tiziano Danilo,Nevsimalova Sona,Nicole Sophie,Neville Brian,van den Maagdenberg Arn M. J. M.,Mikati Mohamad,Goldstein David B.,Vavassori Rosaria,Arzimanoglou Alexis, ,

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference48 articles.

1. Verret S, Steele JC. Alternating hemiplegia in childhood: a report of eight patients with complicated migraine beginning in infancy. Pediatrics. 1971;47:675–80.

2. Dittrich J, Havlová M, Nevsímalová S. Paroxysmal hemipareses in childhood. Dev Med Child Neurol. 1979;21:800–7.

3. Krägeloh I, Aicardi J. Alternating hemiplegia in infants: report of five cases. Dev Med Child Neurol. 1980;22:784–91.

4. Aicardi J, Bourgeois M, Goutières F. Alternating hemiplegia of childhood: clinical findings and diagnostic criteria. In: Andermann F, Aicardi J, Vigevano F, editors. Alternating hemiplegia of childhood. New York: Raven; 1995. p. 3–18.

5. Sweney MT, Silver K, Gerard-Blanluet M, Pedespan JM, Renault F, Arzimanoglou A, et al. Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome. Pediatrics. 2009;123:e534–41.

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