Results 111 to 120 of about 34,604,755 (154)

Familial hemiplegic migraine type 2 with cerebral vasospasm and acute encephalopathy caused by an <i>ATP1A2</i> gene variant: a case report. [PDF]

Transl Pediatr
Liu M, Song Z, Ding C.
europepmc   +1 more source

An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation. [PDF]

BBA Clin, 2014
Kono S, Terada T, Ouchi Y, Miyajima H.
europepmc   +1 more source

When Hemiplegic Migraine Defies Expectations: Diagnostic Complexity in a Rare Genetic Disorder. [PDF]

Case Rep Neurol
Goossens A, Delabie AL, Demaret T, Karadurmus D, Pignato V.   +4 more
europepmc   +1 more source

From Stroke Suspicion to Genetic Confirmation: Familial Hemiplegic Migraine Type 2 as a Rare Stroke Mimic With Persistent Hemiplegia. [PDF]

Cureus
Haggag M, Hussaini S, Shehabeldein A, Muhammad S.   +3 more
europepmc   +1 more source

Familial hemiplegic migraine, epilepsy, and a suspicion of intracranial hypertension in a patient with a positive family history. [PDF]

Arch Med Sci
Grodzka O, Chądzyński P, Makulec A, Domitrz I.   +3 more
europepmc   +1 more source

CACNA1A Genetic Variants and Their Potential Involvement in Migraine Pathogenesis. [PDF]

Int J Mol Sci
Szymanowicz O, Słowikowski B, Poszwa J, Goutor U, Wiszniewska M, Jagodziński PP, Kozubski W, Dorszewska J.   +7 more
europepmc   +1 more source

Adams-Oliver Syndrome Type 3: A Case Report of Concurrent RBPJ, CACNA1A, and Double-Heterozygous MTHFR Variants. [PDF]

Diagnostics (Basel)
Damian GC, Belengeanu V, Popescu C, Marian D, Popovici RA, Cojocariu C.   +5 more
europepmc   +1 more source

Familial hemiplegic migraine due to CACNA1A and PNKD mutations in epilepsy with forced normalization: A case report. [PDF]

Medicine (Baltimore)
Arritola-Uriarte A, San-Juan D, Sandoval-Luna LV, Anschel DJ, Guechi A.   +4 more
europepmc   +1 more source

Genetic Insights into Hemiplegic Migraine: Whole Exome Sequencing Highlights Vascular Pathway Involvement via Association Analysis. [PDF]

Genes (Basel)
Molaee Z, Smith RA, Maksemous N, Griffiths LR.   +3 more
europepmc   +1 more source

Pediatric migraine: Neurodevelopmental mechanisms, clinical phenotypes, and modern therapeutics. [PDF]

World J Clin Pediatr
Al-Beltagi M.
europepmc   +1 more source