Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2
L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - journals.plos.org
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …
Enhanced susceptibility to cortical spreading depression in two types of Na+,K+-ATPase α2 subunit-deficient mice as a model of familial hemiplegic migraine 2
M Unekawa, K Ikeda, Y Tomita, K Kawakami… - …, 2018 - journals.sagepub.com
Background Patients with familial hemiplegic migraine type 2 (FHM2) have a mutated
ATP1A2 gene (encoding Na+, K+-ATPase α2 subunit) and show prolonged migraine aura …
ATP1A2 gene (encoding Na+, K+-ATPase α2 subunit) and show prolonged migraine aura …
Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2
C Capuani, M Melone, A Tottene, L Bragina… - EMBO Molecular …, 2016 - embopress.org
Migraine is a common disabling brain disorder. A subtype of migraine with aura (familial
hemiplegic migraine type 2: FHM 2) is caused by loss‐of‐function mutations in α2 Na+, K+ …
hemiplegic migraine type 2: FHM 2) is caused by loss‐of‐function mutations in α2 Na+, K+ …
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures
A Gallanti, A Tonelli, V Cardin, G Bussone… - Journal of the …, 2008 - Elsevier
Familial hemiplegic migraine (FHM) is a severe dominant form of migraine with aura
associated with transient hemiparesis. Several other neurological signs and symptoms can …
associated with transient hemiparesis. Several other neurological signs and symptoms can …
Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1
K Eikermann-Haerter, E Dileköz… - The Journal of …, 2009 - Am Soc Clin Investig
Familial hemiplegic migraine type 1 (FHM1) is an autosomal dominant subtype of migraine
with aura that is associated with hemiparesis. As with other types of migraine, it affects …
with aura that is associated with hemiparesis. As with other types of migraine, it affects …
Two de novo mutations in the Na, K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine
KRJ Vanmolkot, EE Kors, U Turk… - European journal of …, 2006 - nature.com
Familial hemiplegic migraine (FHM) is a rare autosomal dominantly inherited subtype of
migraine, in which hemiparesis occurs during the aura. The majority of the families carry …
migraine, in which hemiparesis occurs during the aura. The majority of the families carry …
[HTML][HTML] Familial hemiplegic migraine
D Pietrobon - Neurotherapeutics, 2007 - Elsevier
Familial hemiplegic migraine (FHM) is a rare and genetically heterogeneous autosomal
dominant subtype of migraine with aura. Mutations in the genes CACNA1A and SCNA1A …
dominant subtype of migraine with aura. Mutations in the genes CACNA1A and SCNA1A …
Role of different voltage-gated Ca2+ channels in cortical spreading depression: Specific requirement of P/Q-type Ca2+ channels
A Tottene, A Urbani, D Pietrobon - Channels, 2011 - Taylor & Francis
Gain-of-function mutations in CaV2. 1 (P/Q-type) Ca2+ channels cause familial hemiplegic
migraine type 1 (FHM1), a subtype of migraine with aura. Knockin (KI) mice carrying FHM1 …
migraine type 1 (FHM1), a subtype of migraine with aura. Knockin (KI) mice carrying FHM1 …
Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice
K Eikermann-Haerter, I Yuzawa, T Qin… - Journal of …, 2011 - Soc Neuroscience
Familial hemiplegic migraine type 1, a monogenic migraine variant with aura, is linked to
gain-of-function mutations in the CACNA1A gene encoding CaV2. 1 channels. The S218L …
gain-of-function mutations in the CACNA1A gene encoding CaV2. 1 channels. The S218L …
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
MA Kaunisto, H Harno, KRJ Vanmolkot, JJ Gargus… - Neurogenetics, 2004 - Springer
Familial hemiplegic migraine (FHM), a rare autosomal dominant subtype of migraine with
aura, has been linked to two chromosomal loci, 19p13 and 1q23. Mutations in the Na+, K+ …
aura, has been linked to two chromosomal loci, 19p13 and 1q23. Mutations in the Na+, K+ …