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Familial hemiplegic migraine type 2
- ... ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by migraine headaches ...
- ... 1002/humu.20178. Citation on PubMed Pietrobon D. Familial hemiplegic ... epilepsy with febrile seizures plus type 2. J Neurosci. 2001 Oct 1;21(19): ...
- ... CACNA1A gene have been identified in people with familial hemiplegic migraine type 1 (FHM1). This condition is characterized by migraines ... Luvisetto S, Striessnig J, Fletcher C, Pietrobon D. Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and ...
- ... ClinicalTrials.gov MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1 MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3 PubMed Black DF. Sporadic ...
- ... hemiplegic migraine National Organization for Rare Disorders (NORD) MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 PubMed de Vries B, Freilinger T, Vanmolkot ... The genetic features of 24 patients affected by familial and sporadic ... Sci. 2011 May;32 Suppl 1:S141-2. doi: 10.1007/s10072-011-0517-4. Citation ...
- ... begin in infancy and usually disappear by age 2. ICCA is characterized by both ... hemiplegic migraine (described above) can also cause BFIS and ICCA. ...
- ... head.People with migraine, particularly women who have migraine with aura, have an increased risk of a type of stroke that is caused by a lack of blood flow to the brain (ischemic stroke), but this is a rare ... hemiplegic migraine and sporadic hemiplegic migraine are characterized by ...