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Results 1 - 7 of 7 for "Migraine," familial "hemiplegic," 2
  1. ... NORD) ClinicalTrials.gov MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1 MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3 PubMed Black ...
  2. ... 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 ...
  3. ... ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by migraine headaches ... 0000127310.11526.fd. Citation on PubMed Pietrobon D. Familial hemiplegic migraine. Neurotherapeutics. 2007 Apr;4(2):274-84. doi: 10.1016/j.nurt.2007. ...
  4. ... Luvisetto S, Striessnig J, Fletcher C, Pietrobon D. Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and ...
  5. ... 1002/humu.20178. Citation on PubMed Pietrobon D. Familial hemiplegic migraine. Neurotherapeutics. 2007 Apr;4(2):274-84. doi: 10.1016/j.nurt.2007. ...
  6. ... begin in infancy and usually disappear by age 2. ICCA is characterized by both ... hemiplegic migraine (described above) can also cause BFIS and ICCA. ...
  7. ... usually include additional signs and symptoms. For example, familial hemiplegic migraine and sporadic hemiplegic migraine are characterized by migraine ...