Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review. [electronic resource]
- Neuropediatrics 06 2020
- 215-220 p. digital
Publication Type: Case Reports; Journal Article; Review
1439-1899
10.1055/s-0039-3400986 doi
Acute Disease Adolescent Brain Diseases--diagnosis Female Humans Intellectual Disability--diagnosis Migraine with Aura--complications Mutation Seizures--diagnosis Severity of Illness Index Sodium-Potassium-Exchanging ATPase--genetics