Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.
Marzin, Pauline
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations. [electronic resource] - Brain & development Oct 2018 - 768-774 p. digital
Publication Type: Case Reports; Journal Article; Video-Audio Media
1872-7131
10.1016/j.braindev.2018.05.008 doi
Adolescent
Brain--physiopathology
Child
Child, Preschool
Epilepsy--diagnosis
Female
Hemiplegia--genetics
Humans
Male
Movement Disorders--diagnosis
Mutation
Seizures--diagnosis
Sodium-Potassium-Exchanging ATPase--genetics
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations. [electronic resource] - Brain & development Oct 2018 - 768-774 p. digital
Publication Type: Case Reports; Journal Article; Video-Audio Media
1872-7131
10.1016/j.braindev.2018.05.008 doi
Adolescent
Brain--physiopathology
Child
Child, Preschool
Epilepsy--diagnosis
Female
Hemiplegia--genetics
Humans
Male
Movement Disorders--diagnosis
Mutation
Seizures--diagnosis
Sodium-Potassium-Exchanging ATPase--genetics