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Times Cited
Times Co-cited
Similarity
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
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Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
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Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Kaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, Gisela M Terwindt, Joost Haan, Wil A J Hoefnagels, David F Black, Lodewijk A Sandkuijl, Rune R Frants, Michel D Ferrari,[...]. Ann Neurol 2003
Kaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, Gisela M Terwindt, Joost Haan, Wil A J Hoefnagels, David F Black, Lodewijk A Sandkuijl, Rune R Frants, Michel D Ferrari,[...]. Ann Neurol 2003
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The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
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A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.
Maria Spadaro, Simona Ursu, Frank Lehmann-Horn, Liana Veneziano, Giovanni Antonini, Paola Giunti, Marina Frontali, Karin Jurkat-Rott. Neurogenetics 2004
Maria Spadaro, Simona Ursu, Frank Lehmann-Horn, Liana Veneziano, Giovanni Antonini, Paola Giunti, Marina Frontali, Karin Jurkat-Rott. Neurogenetics 2004
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ATP1A2 mutations in 11 families with familial hemiplegic migraine.
Florence Riant, Maurizio De Fusco, Paolo Aridon, Anne Ducros, Claire Ploton, Florence Marchelli, Jacqueline Maciazek, Marie Germaine Bousser, Giorgio Casari, Elisabeth Tournier-Lasserve. Hum Mutat 2005
Florence Riant, Maurizio De Fusco, Paolo Aridon, Anne Ducros, Claire Ploton, Florence Marchelli, Jacqueline Maciazek, Marie Germaine Bousser, Giorgio Casari, Elisabeth Tournier-Lasserve. Hum Mutat 2005
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Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
Kathryn J Swoboda, Emmanuel Kanavakis, Athina Xaidara, Justine E Johnson, Mark F Leppert, Mylynda B Schlesinger-Massart, Louis J Ptacek, Kenneth Silver, Sotiris Youroukos. Ann Neurol 2004
Kathryn J Swoboda, Emmanuel Kanavakis, Athina Xaidara, Justine E Johnson, Mark F Leppert, Mylynda B Schlesinger-Massart, Louis J Ptacek, Kenneth Silver, Sotiris Youroukos. Ann Neurol 2004
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Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
K R J Vanmolkot, H Stroink, J B Koenderink, E E Kors, J J M W van den Heuvel, E H van den Boogerd, A H Stam, J Haan, B B A De Vries, G M Terwindt,[...]. Ann Neurol 2006
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A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
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Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.
Jan B Koenderink, Giovanni Zifarelli, Li Yan Qiu, Wolfgang Schwarz, Jan Joep H H M De Pont, Ernst Bamberg, Thomas Friedrich. Biochim Biophys Acta 2005
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A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
M A Kaunisto, H Harno, K R J Vanmolkot, J J Gargus, G Sun, E Hämäläinen, E Liukkonen, M Kallela, A M J M van den Maagdenberg, R R Frants,[...]. Neurogenetics 2004
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Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
A Ambrosini, M D'Onofrio, G S Grieco, A Di Mambro, G Montagna, D Fortini, F Nicoletti, G Nappi, G Sances, J Schoenen,[...]. Neurology 2005
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Epilepsy as part of the phenotype associated with ATP1A2 mutations.
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Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
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The genetic spectrum of a population-based sample of familial hemiplegic migraine.
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Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2.
Laura Segall, Alessandra Mezzetti, Rosemarie Scanzano, J Jay Gargus, Enrico Purisima, Rhoda Blostein. Proc Natl Acad Sci U S A 2005
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Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.
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A novel ATP1A2 mutation in a family with FHM type II.
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A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.
L L Thomsen, M K Eriksen, S F Roemer, I Andersen, J Olesen, M B Russell. Brain 2002
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Mechanisms of migraine aura revealed by functional MRI in human visual cortex.
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Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.
B de Vries, T Freilinger, K R J Vanmolkot, J B Koenderink, A H Stam, G M Terwindt, E Babini, E H van den Boogerd, J J M W van den Heuvel, R R Frants,[...]. Neurology 2007
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CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.
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Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.
Neslihan N Tavraz, Thomas Friedrich, Katharina L Dürr, Jan B Koenderink, Ernst Bamberg, Tobias Freilinger, Martin Dichgans. J Biol Chem 2008
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A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.
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Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
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Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Kaate R J Vanmolkot, Esther E Kors, Ulku Turk, Dylsad Turkdogan, Antoine Keyser, Ludo A M Broos, Sima Kheradmand Kia, Jeroen J M W van den Heuvel, David F Black, Joost Haan,[...]. Eur J Hum Genet 2006
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The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Kaate R J Vanmolkot, Elena Babini, Boukje de Vries, Anine H Stam, Tobias Freilinger, Gisela M Terwindt, Lisa Norris, Joost Haan, Rune R Frants, Nabih M Ramadan,[...]. Hum Mutat 2007
Kaate R J Vanmolkot, Elena Babini, Boukje de Vries, Anine H Stam, Tobias Freilinger, Gisela M Terwindt, Lisa Norris, Joost Haan, Rune R Frants, Nabih M Ramadan,[...]. Hum Mutat 2007
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New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
Katell Beauvais, Florence Cavé-Riant, Claire De Barace, Marc Tardieu, Elisabeth Tournier-Lasserve, Alain Furby. Eur Neurol 2004
Katell Beauvais, Florence Cavé-Riant, Claire De Barace, Marc Tardieu, Elisabeth Tournier-Lasserve, Alain Furby. Eur Neurol 2004
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Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.
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Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
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Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
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Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine.
Lise L Thomsen, Elsebet Ostergaard, Jes Olesen, Michael B Russell. Neurology 2003
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Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.
Gisela Terwindt, Esther Kors, Joost Haan, Frans Vermeulen, Arn Van den Maagdenberg, Rune Frants, Michel Ferrari. Arch Neurol 2002
Gisela Terwindt, Esther Kors, Joost Haan, Frans Vermeulen, Arn Van den Maagdenberg, Rune Frants, Michel Ferrari. Arch Neurol 2002
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Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Laura Segall, Rosemarie Scanzano, Mari A Kaunisto, Maija Wessman, Aarno Palotie, J Jay Gargus, Rhoda Blostein. J Biol Chem 2004
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First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
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Molecular genetics of migraine.
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Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
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Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
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Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes.
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The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice.
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A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
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Crystal structure of the sodium-potassium pump.
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Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
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High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
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Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
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A gene for familial hemiplegic migraine maps to chromosome 19.
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Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.