|1.||Lykke-Hartmann, Karin: 2 articles (12/2013 - 02/2012)|
|2.||Nishiyama, Kazutoshi: 1 article (03/2015)|
|3.||Kaneko, Juntaro: 1 article (03/2015)|
|4.||Hamada, Junichi: 1 article (03/2015)|
|5.||Tominaga, Naomi: 1 article (03/2015)|
|6.||Iizuka, Takahiro: 1 article (03/2015)|
|7.||Sato, Mayumi: 1 article (03/2015)|
|8.||Akutsu, Tsugio: 1 article (03/2015)|
|9.||Sakai, Fumihiko: 1 article (03/2015)|
|10.||Russel, Frans G M: 1 article (07/2014)|
|1.||Migraine with Aura (Familial Hemiplegic Migraine)
06/01/2011 - "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 exclusively expressed in astrocytes in the adult brain. "
01/01/2004 - "Familial hemiplegic migraine type 2, an autosomal dominant form of migraine with aura, has been associated with four distinct mutations in the alpha2-subunit of the Na+,K+-ATPase. "
06/01/2004 - "Studies on the genetics of familial hemiplegic migraine revealed, in addition to the previously identified familial hemiplegic migraine type 1 gene CACNA1A on chromosome 19, the familial hemiplegic migraine type 2 gene ATP1A2, encoding the alpha2-subunit of sodium/potassium pumps. "
08/01/2012 - "Familial forms are dominantly inherited, and are attributable to mutations in genes encoding proteins involved in ion transportation, including ATP1A2, which codes for the α-2 isoform of the sodium-potassium adenosine triphosphatase, a P-type cation transport adenosine triphosphatase, and responsible for the so-called familial hemiplegic migraine type 2. We describe a 9-year-old boy affected by familial hemiplegic migraine, with a novel ATP1A2 gene mutation (c.1799T>C p.V600A) in exon 13. "
|2.||Migraine Disorders (Migraine)
04/01/2008 - "Familial hemiplegic migraine type 2 (FHM-2) and common types of migraine show phenotypic similarities which may indicate a common neurobiological background. "
03/01/2015 - "Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2."
10/01/2011 - "We describe a child with Familial Hemiplegic Migraine type 2 who showed a transient neuropsychological impairment featuring a nonverbal learning disorder during and after a Hemiplegic migraine attack. "
07/01/2014 - "Sporadic hemiplegic migraine type 2 (SHM2) and familial hemiplegic migraine type 2 (FHM2) are rare forms of hemiplegic migraine caused by mutations in the Na(+),K(+)-ATPase α2 gene. "
01/01/2008 - "Mutations in the ATP1A2 gene, encoding the alpha2-subunit of the Na+,K+-ATPase, are associated with familial hemiplegic migraine type 2. The majority of ATP1A2 mutations were reported in patients with hemiplegic migraine without any additional neurological findings. "
|3.||Nervous System Diseases (Neurological Disorders)
12/01/2013 - "Na(+)/K(+)-ATPase mutations are associated with neurological disorders, where mutations in the Na(+)/K(+)-ATPase α2 and α3 isoforms cause Familial hemiplegic migraine type 2 (FHM2) and Rapid-onset dystonia-parkinsonism (RDP)/Alternating hemiplegic childhood (AHC), respectively. "
02/07/2014 - "The neurological disorders familial hemiplegic migraine type 2 (FHM2), alternating hemiplegia of childhood (AHC), and rapid-onset dystonia parkinsonism (RDP) are caused by mutations of Na(+),K(+)-ATPase α2 and α3 isoforms, expressed in glial and neuronal cells, respectively. "
|5.||Parkinsonian Disorders (Parkinsonism)
|3.||Adenosine Triphosphatases (ATPase)
|4.||Protein Isoforms (Isoforms)
|6.||Sodium-Potassium-Exchanging ATPase (Sodium, Potassium ATPase)
|7.||Proteins (Proteins, Gene)
|8.||Nitric Oxide (Nitrogen Monoxide)
|9.||Alternating hemiplegia of childhood