| 1 | The genetic features of 24 patients affected by famil ial and sporadic hemiplegic migraine. (21533730) | Gallanti A.... Bassi M.T. | 2011 | ATP1A2 |
| 2 | De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. (20837964) | Riant F.... Tournier-Lasserve E. | 2010 | ATP1A2, CACNA1A |
| 3 | Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine. (19372756) | Tavraz N.N.... Friedrich T. | 2009 | ATP1A2, CACNA1A, SCN1A |
| 4 | Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (18976783) | Veneziano L.... Frontali M. | 2009 | CACNA1A |
| 5 | Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. (19332696) | Vahedi K.... Bousser M.-G. | 2009 | ATP1A2, CACNA1A, SCN1A |
| 6 | Familial hemiplegic migraine type 1 shows no hypersensitivity to nitric oxide. (18384418) | Hansen J.M.... Ashina M. | 2008 | CACNA1A |
| 7 | The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation. (18581134) | Weiss N.... de Waard M. | 2008 | CACNA1A, OPRM1 |
| 8 | CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. (18498393) | De Vries B.... Ferrari M.D. | 2008 | CACNA1A |
| 9 | Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel. (18632931) | Cestele S.... Mantegazza M. | 2008 | SCN1A |
| 10 | Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes. (18644040) | Cuenca-Leon E.... Cormand B. | 2008 | ATP1A2, CACNA1A, MGR |
| 11 | Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation. (18498390) | Lebas A.... Parain D. | 2008 | ATP1A2 |
| 12 | Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients. (18513263) | Thomsen L.... Olesen J. | 2008 | ATP1A2, CACNA1A |
| 13 | Calcitonin gene-related peptide does not cause the familial hemiplegic migraine phenotype. (18779512) | Hansen J.M.... Ashina M. | 2008 | ATP1A2, CALCA |
| 14 | Divergent sodium channel defects in familial hemiplegic migraine. (18621678) | Kahlig K.M.... George A.L. | 2008 | SCN1A |
| 15 | Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation. (18313928) | Chan Y.C.... Ong B.K. | 2008 | CACNA1A |
| 16 | Familial hemiplegic migraine type 2 does not share hypersensitivity to nitric oxide with common types of migraine. (18294248) | Hansen J.M.... Ashina M. | 2008 | ATP1A2 |
| 17 | CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine. (18400034) | Stam A.H.... Terwindt G.M. | 2008 | CACNA1A |
| 18 | Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. (18279427) | Freilinger T.... Knoblauch H. | 2008 | CACNA1A |
| 19 | First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine. (17473835) | Vanmolkot K.R.... van den Maagdenberg A.M. | 2007 | ATP1A2, CACNA1A |
| 20 | Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine. (17952365) | Castro M.J.... van den Maagdenberg A.M. | 2007 | ATP1A2 |
| 21 | Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine. (17877748) | Tonelli A.... Bassi M.T. | 2007 | ATP1A2, CACNA1A, SCN1A |
| 22 | The genetic spectrum of a population-based sample of familial hemiplegic migraine. (17142831) | Thomsen L.L.... Olesen J. | 2007 | ATP1A2, CACNA1A, SCN1A |
| 23 | Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. (18021921) | Gargus J.J.... Tournay A. | 2007 | SCN1A |
| 24 | Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. (16538223) | Vanmolkot K.R.... van den Maagdenberg A.M. | 2006 | ATP1A2 |
| 25 | Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. (16054936) | Dichgans M.... Strom T.M. | 2005 | ATP1A2, CACNA1A, SCN5A |
| 26 | Single-fiber EMG in familial hemiplegic migraine. (15557518) | Terwindt G.M.... van Dijk J.G. | 2004 | CACNA1A |
| 27 | Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants. (15159495) | Jurkat-Rott K.... Dichgans M. | 2004 | ATP1A2 |
| 28 | Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. (15174025) | Swoboda K.J.... Youroukos S. | 2004 | ATP1A2 |
| 29 | New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus. (15240985) | Beauvais K.... Furby A. | 2004 | CACNA1A |
| 30 | A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. (15133718) | Kaunisto M.A.... Wessman M. | 2004 | ATP1A2 |
| 31 | Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2. (15308625) | Segall L.... Blostein R. | 2004 | ATP1A2 |
| 32 | Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine. (12756131) | Kors E.E.... Ferrari M.D. | 2003 | CACNA1A |
| 33 | Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. (12953268) | Vanmolkot K.R.J.... van den Maagdenberg A.M.J.M. | 2003 | ATP1A2, CACNA1A |
| 34 | Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. (12707077) | Alonso I.... Coutinho P. | 2003 | CACNA1A |
| 35 | The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells. (12527722) | Melliti K.... Seabrook G.R. | 2003 | CACNA1A, GNB1, GNG2 |
| 36 | Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing. (12705332) | Wieser T.... Deufel T. | 2003 | CACNA1A |
| 37 | Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons. (12235360) | Tottene A.... Pietrobon D. | 2002 | CACNA1A |
| 38 | Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene. (11971066) | Takahashi T.... Tsuji S. | 2002 | CACNA1A |
| 39 | Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. (11735221) | Jones K.W.... Peroutka S.J. | 2001 | MGR5 |
| 40 | Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. (11409427) | Kors E.E.... Ferrari M.D. | 2001 | CACNA1A |
| 41 | Familial hemiplegic migraine (15775664) | Takahashi T.... Tsuji S. | 2001 | CACNA1A |
| 42 | Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene. (11167897) | Haan J.... Ferrari . | 2000 | CACNA1A |
| 43 | CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy. (11061267) | Vahedi K.... Bousser M.G. | 2000 | CACNA1A |
| 44 | Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene. (10668728) | Chabriat H.... Bousser M.G. | 2000 | CACNA1A |
| 45 | A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia. (10408534) | Battistini S.... Carrera P. | 1999 | CACNA1A |
| 46 | Genetic heterogeneity in Italian families with familial hemiplegic migraine. (10408532) | Carrera P.... Gelfi C. | 1999 | CACNA1A |
| 47 | Familial hemiplegic migraine: involvement of a calcium neuronal channel. (9436352) | Ophoff R.A.... Ferrari M.D. | 1997 | CACNA1A |
| 48 | Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome. (9579893) | Terwindt G.M.... Ferrari M.D. | 1997 | ATP1A2 |
| 49 | Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. (8898206) | Ophoff R.A.... Frants R.R. | 1996 | CACNA1A |
| 50 | A gene for familial hemiplegic migraine maps to chromosome 19. (8220421) | Joutel A.... Weissenbach J. | 1993 | CACNA1A |
