Results 131 to 140 of about 5,459 (165)

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

EEG patterns in each phase of hemiplegic migraine: a systematic review and pooled prevalence meta-analysis. [PDF]

J Headache Pain
Kedgan P, Anukoolwittaya P, Surawattanawong T, Thanprasertsuk S, Rattanawong W, Limotai C.   +5 more
europepmc   +1 more source

Migraine in children and adolescents. [PDF]

Dev Med Child Neurol
Abu-Arafeh I.
europepmc   +1 more source

Molecular and clinical heterogeneity in an Iranian case series of Joubert syndrome. [PDF]

Mol Genet Metab Rep
Khalilian S, Fathi M, Farbood Z, Dehghanian F, Masoudi M, Ghafouri-Fard S, Dastgheib SA, Miryounesi M.   +7 more
europepmc   +1 more source

Neuro-Ophthalmological Manifestations of Episodic Ataxia Type 2 Due to a Novel CACNA1A Mutation. [PDF]

Mov Disord Clin Pract
Asad M, Murphy O, Healy DG, Fearon C.
europepmc   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia. [PDF]

Ann Clin Transl Neurol
Cameron D, Clifton NE, de la Fuente DC, Holmans P, Bray NJ, Peall KJ.   +5 more
europepmc   +1 more source

Artificial intelligence-assisted clinical exome sequencing: Insights and outcomes from 822 pediatric diagnoses. [PDF]

Genet Med Open
Pan Y, Danley P, Kramer T, Noruzinia M, Buser K, Yatsenko AN, Bellissimo D, Guo F.   +7 more
europepmc   +1 more source

Polymorphisms in CACNA1A, CACNA1C, and CACNA1H Genes in Korean Pediatric Patients with Developmental Delay and Intellectual Disability: A Focus on Epilepsy Comorbidity. [PDF]

Genes (Basel)
Han JY.
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

Increased Prevalence of Rare Copy Number Variants in Australian Children With Fetal Alcohol Spectrum Disorder: Experience in a State-Wide Diagnostic Service. [PDF]

Alcohol Clin Exp Res (Hoboken)
Byrnes S, Collins F, Elliott E.
europepmc   +1 more source