Results 1 -
7
of
7
for
"Migraine," familial "hemiplegic," 3
- ... Registry: Migraine, familial hemiplegic, 2 Genetic Testing Registry: Migraine, familial hemiplegic, 3 Familial hemiplegic migraine National Organization for Rare Disorders ( ...
- ... SCN1A gene have been identified in people with familial hemiplegic migraine type 3 (FHM3), a form of migraine headache that runs in families. Each of these mutations changes a single protein ...
- ... Lasserve E. ATP1A2 mutations in 11 families with familial hemiplegic migraine. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Citation on ... by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine. Channels (Austin). 2009 Mar-Apr;3(2):82-7. doi: 10.4161/chan.3. ...
- ... Russel FG, Koenderink JB. Biochemical characterization of sporadic/familial hemiplegic migraine mutations. Biochim Biophys Acta. 2014 Jul;1838(7):1693-700. doi: 10.1016/j.bbamem.2014.03.022. Epub 2014 Apr 3. Citation on PubMed
- ... Complex Assembly. Cell Rep. 2018 Jan 16;22(3):820-831. doi: ... torticollis and hemiplegic migraine. Dev Med Child Neurol. 2012 Oct;54(10): ...
- ... CACNA1A gene have been identified in people with familial hemiplegic migraine type 1 (FHM1). This condition is characterized by ... a dozen families. The CACNA1A variants that cause familial hemiplegic migraine are called gain-of-function variants, because they ...
- ... usually include additional signs and symptoms. For example, familial hemiplegic migraine and sporadic hemiplegic migraine are characterized by migraine ...