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Journal article
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Panagiotakaki, Eleni
De Grandis, Elisa
Stagnaro, Michela
Heinzen, Erin L
Fons, Carmen
Sisodiya, Sanjay
de Vries, Boukje
Goubau, Christophe
[UCL]
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
Italian IBAHC Consortium
French AHC Consortium
International AHC Consortium
(2015)
Orphanet Journal of Rare Diseases — Vol. 10, no. 1, p. 123 [1-13] (2015)