Disease: Headache ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018681
Disease: Headache
Headache 		0.060 Biomarker phenotype BEFREE The clinical notes of the remaining 11 patients (4 with familial hemiplegic migraine [FHM] and 7 with sporadic hemiplegic migraine [SHM]) were reviewed, and the frequency and description of their headaches and aura before and after receiving onabotulinumtoxinA were recorded. 29762872 2018
CUI: C0018681
Disease: Headache
Headache 		0.060 Biomarker phenotype BEFREE Case description We report on the emergency personalized treatment protocol used in an 11 year-old girl with CACNA1A-related encephalopathy for the management of acute attacks of headache, hemiconvulsions and hemiplegia with coma. 27651281 2017
CUI: C0018681
Disease: Headache
Headache 		0.060 Biomarker phenotype BEFREE Channeling headache: novel findings in the study of Ca(2+)-channels and FHM-1. 22991044 2013
CUI: C0018681
Disease: Headache
Headache 		0.060 GeneticVariation phenotype BEFREE A novel CACNA1A mutation results in episodic ataxia with migrainous features without headache. 22942164 2012
CUI: C0018681
Disease: Headache
Headache 		0.060 Biomarker phenotype BEFREE Sporadic and familial hemiplegic migraines (SHM and FHM) are rare paroxysmal disorders characterized by motor aura and headache. 20187861 2010
CUI: C0018681
Disease: Headache
Headache 		0.060 GeneticVariation phenotype LHGDN Stepwise developmental regression associated with novel CACNA1A mutation. 18940563 2008