Search Results - "Camiña, Montserrat"

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  1. 1
    SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population

    SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population by Carreño, Oriel, Corominas, Roser, Fernández-Morales, Jessica, Camiña, Montserrat, Sobrido, María-Jesús, Fernández-Fernández, José Manuel, Pozo-Rosich, Patricia, Cormand, Bru, Macaya, Alfons

    “…The transient receptor potential (TRP) superfamily of non‐selective cationic channels are involved in several processes plausibly relevant to migraine…”
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  2. 2
    Two-stage case-control association study of dopamine-related genes and migraine

    Two-stage case-control association study of dopamine-related genes and migraine by Corominas, Roser, Ribases, Marta, Camiña, Montserrat, Cuenca-León, Ester, Pardo, Julio, Boronat, Susana, Sobrido, María-Jesús, Cormand, Bru, Macaya, Alfons

    Published in BMC genetics (21-09-2009)
    “…We previously reported risk haplotypes for two genes related with serotonin and dopamine metabolism: MAOA in migraine without aura and DDC in migraine with…”
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  3. 3
    Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico

    Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico by Sesar, Angel, Cacheiro, Pilar, López-López, Marisol, Camiña-Tato, Montserrat, Quintáns, Beatriz, Monroy-Jaramillo, Nancy, Alonso-Vilatela, María-Elisa, Cebrián, Ernesto, Yescas-Gómez, Petra, Ares, Begoña, Rivas, María-Teresa, Castro, Alfonso, Carracedo, Angel, Sobrido, María-Jesús

    Published in Journal of the neurological sciences (15-03-2016)
    “…Abstract Introduction The pathophysiology of PD (Parkinson's disease) has been related to the ubiquitin proteasome system and oxidative stress. Parkin acts as…”
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  4. 4
    mtDNA nt13708A variant increases the risk of multiple sclerosis

    mtDNA nt13708A variant increases the risk of multiple sclerosis by Yu, Xinhua, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A, Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I, Mørk, Sverre J, Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G, Myhr, Kjell-Morten, Epplen, Joerg T, Saarela, Janna, Ibrahim, Saleh M

    Published in PloS one (13-02-2008)
    “…Mitochondrial DNA (mtDNA) polymorphism is a possible factor contributing to the maternal parent-of-origin effect in multiple sclerosis (MS) susceptibility. In…”
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