Related references
Note: Only part of the references are listed.Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation
Takahiro Iizuka et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline
T. Freilinger et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2011)
Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management
Michael Bjorn Russell et al.
LANCET NEUROLOGY (2011)
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutation identified in sporadic or familial hemiplegic migraine
Neslihan N. Tavraz et al.
CHANNELS (2009)
Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation
T. Freilinger et al.
CEPHALALGIA (2008)
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine
B. de Vries et al.
NEUROLOGY (2007)
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation
KRJ Vanmolkot et al.
ANNALS OF NEUROLOGY (2006)
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
K Jurkat-Rott et al.
NEUROLOGY (2004)
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
M De Fusco et al.
NATURE GENETICS (2003)