Disease: Hemiplegic migraine ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		0.050 Biomarker disease BEFREE Involvement of CACNA1A, ATP1A2 and SCN1A was studied using whole exome sequencing data from 293 patients with hemiplegic migraine. 29486580 2018
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		0.050 GeneticVariation disease BEFREE Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine. 23398611 2013
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		0.050 GeneticVariation disease BEFREE Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy. 19220312 2009
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		0.050 GeneticVariation disease BEFREE Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		0.050 GeneticVariation disease BEFREE Here, we report the genetic analysis of four families and one sporadic case with hemiplegic migraine (HM) in whom we searched for mutations in the three genes associated with the disease CACNA1A, ATP1A2 and SCN1A. 17877748 2007