论文信息 - Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrum. - 字舞流文

Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrum.

E. Bertini | Massimiliano Valeriani | A. Capuano | N. Nardocci | F. Vigevano | B. Garavaglia | F. Nicita | L. Travaglini | C. Panteghini | S. Sabatini

[1] E. Veneselli,et al. Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism , 2014, Neurology.

[2] A. Brashear,et al. ATP1A3 mutations , 2014, Neurology.

[3] Allison Brashear,et al. ATP1A3 mutations in infants: a new rapid‐onset dystonia–Parkinsonism phenotype characterized by motor delay and ataxia , 2012, Developmental medicine and child neurology.

[4] M. Stacy,et al. Psychiatric disorders in rapid-onset dystonia-parkinsonism , 2012, Neurology.

[5] Matthew T. Sweney,et al. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond. , 2015, Pediatric neurology.