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Filter Applied: paroxysmal neurologic deficits (Click to remove)

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation
Brain 121:127-133, Lugaresi,E.,et al, 1998



Showing articles 0 to 3 of 3