Ribasés M - Search Results

1

Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.

Garcia-Martínez I, Sánchez-Mora C, Pagerols M, Richarte V, Corrales M, Fadeuilhe C, Cormand B, Casas M, Ramos-Quiroga JA, Ribasés M. Garcia-Martínez I, et al. Among authors: ribases m. Transl Psychiatry. 2016 Aug 30;6(8):e879. doi: 10.1038/tp.2016.151. Transl Psychiatry. 2016. PMID: 27576168 Free PMC article.

2

[Large-scale genotyping in research into autism spectrum disorders and attention deficit hyperactivity disorder].

Bayés M, Ramos JA, Cormand B, Hervas-Zúñiga A, del Campo M, Duran-Tauleria E, Ribasés M, Vilella-Cuadrada E, de Diego-Otero Y, Casas-Brugué M, Estivill X. Bayés M, et al. Among authors: ribases m. Rev Neurol. 2005 Jan 15;40 Suppl 1:S187-90. Rev Neurol. 2005. PMID: 15736086 Free article. Spanish.

3

Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.

Guzmán B, Cormand B, Ribasés M, González-Núñez D, Botey A, Poch E. Guzmán B, et al. Among authors: ribases m. Hypertension. 2006 Nov;48(5):883-91. doi: 10.1161/01.HYP.0000244085.52918.a0. Epub 2006 Oct 2. Hypertension. 2006. PMID: 17015768

4

Brain-derived neurotrophic factor and its intracellular signaling pathways in cocaine addiction.

Corominas M, Roncero C, Ribases M, Castells X, Casas M. Corominas M, et al. Among authors: ribases m. Neuropsychobiology. 2007;55(1):2-13. doi: 10.1159/000103570. Epub 2007 Jun 8. Neuropsychobiology. 2007. PMID: 17556847 Free article. Review.

5

A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: clinical, biochemical and genetic analysis.

Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal A, García-Cazorla A, Pérez-Dueñas B, Campistol J, Artuch R, Cormand B. Ribasés M, et al. Mol Genet Metab. 2007 Nov;92(3):274-7. doi: 10.1016/j.ymgme.2007.07.004. Epub 2007 Aug 14. Mol Genet Metab. 2007. PMID: 17698383

6

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.

Ribasés M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, Artigas J, Rodriguez-Ben S, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Mol Psychiatry. 2009 Jan;14(1):71-85. doi: 10.1038/sj.mp.4002100. Epub 2007 Oct 16. Mol Psychiatry. 2009. PMID: 17938636

7

Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder.

Ribasés M, Hervás A, Ramos-Quiroga JA, Bosch R, Bielsa A, Gastaminza X, Fernández-Anguiano M, Nogueira M, Gómez-Barros N, Valero S, Gratacòs M, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Biol Psychiatry. 2008 May 15;63(10):935-45. doi: 10.1016/j.biopsych.2007.11.004. Epub 2008 Jan 7. Biol Psychiatry. 2008. PMID: 18179783

8

[Hyperkalemic periodic paralysis: a Spanish family with the p.Thr704Met mutation in the SCN4A gene].

Narberhaus B, Cormand B, Cuenca-León E, Ribasés M, Monells J. Narberhaus B, et al. Among authors: ribases m. Neurologia. 2008 Sep;23(7):427-35. Neurologia. 2008. PMID: 18726720 Spanish.

9

Lack of association of hormone receptor polymorphisms with migraine.

Corominas R, Ribasés M, Cuenca-León E, Cormand B, Macaya A. Corominas R, et al. Among authors: ribases m. Eur J Neurol. 2009 Mar;16(3):413-5. doi: 10.1111/j.1468-1331.2008.02499.x. Eur J Neurol. 2009. PMID: 19175383

10

Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population.

Corominas R, Ribasés M, Cuenca-León E, Narberhaus B, Serra SA, del Toro M, Roig M, Fernández-Fernández JM, Macaya A, Cormand B. Corominas R, et al. Among authors: ribases m. Neurosci Lett. 2009 May 15;455(2):105-9. doi: 10.1016/j.neulet.2009.03.011. Epub 2009 Mar 6. Neurosci Lett. 2009. PMID: 19368856

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