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Association study of the serotoninergic system in migraine in the Spanish population.
Corominas R, Sobrido MJ, Ribasés M, Cuenca-León E, Blanco-Arias P, Narberhaus B, Roig M, Leira R, López-González J, Macaya A, Cormand B. Corominas R, et al. Among authors: sobrido mj. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):177-84. doi: 10.1002/ajmg.b.30972. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19455600
SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population.
Carreño O, Corominas R, Fernández-Morales J, Camiña M, Sobrido MJ, Fernández-Fernández JM, Pozo-Rosich P, Cormand B, Macaya A. Carreño O, et al. Among authors: sobrido mj. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):94-103. doi: 10.1002/ajmg.b.32007. Epub 2011 Dec 7. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22162417
Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.
Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg D, Valverde MÁ, Fernández-Fernández JM, Macaya A, Cormand B. Carreño O, et al. Among authors: sobrido mj. Mol Genet Genomic Med. 2013 Nov;1(4):206-22. doi: 10.1002/mgg3.24. Epub 2013 Jul 2. Mol Genet Genomic Med. 2013. PMID: 24498617 Free PMC article.
No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.
Fachal L, Mosquera-Miguel A, Pastor P, Ortega-Cubero S, Lorenzo E, Oterino-Durán A, Toriello M, Quintáns B, Camiña-Tato M, Sesar A, Vega A, Sobrido MJ, Salas A. Fachal L, et al. Among authors: sobrido mj. Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):54-65. doi: 10.1002/ajmg.b.32276. Epub 2014 Oct 28. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25349034
[Cerebral hemorrhage and migraine].
Aldrey JM, Castillo J, Leira R, Suárez P, Sobrido MJ, Noya M. Aldrey JM, et al. Among authors: sobrido mj. Rev Neurol. 1996 Feb;24(126):183-6. Rev Neurol. 1996. PMID: 8714485 Spanish.
A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism.
Blanco-Arias P, Einholm AP, Mamsa H, Concheiro C, Gutiérrez-de-Terán H, Romero J, Toustrup-Jensen MS, Carracedo A, Jen JC, Vilsen B, Sobrido MJ. Blanco-Arias P, et al. Among authors: sobrido mj. Hum Mol Genet. 2009 Jul 1;18(13):2370-7. doi: 10.1093/hmg/ddp170. Epub 2009 Apr 7. Hum Mol Genet. 2009. PMID: 19351654
103 results