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Endothelial NO synthase 786T/T polymorphism increases hemorrhagic transformation after endovascular thrombectomy.
de la Riva P, Rodríguez-Antigüedad J, Gómez V, Arenaza G, Gorostidi A, Díez N, de Arce A, Martínez-Zabaleta M, González F, Luttich A, Garmendia E, Sola A, Larrea JA, Bergareche A, Sobrino T. de la Riva P, et al. Among authors: gorostidi a. Nitric Oxide. 2022 Dec 1;129:8-15. doi: 10.1016/j.niox.2022.08.006. Epub 2022 Sep 5. Nitric Oxide. 2022. PMID: 36067953
Αlpha-synuclein levels in blood plasma from LRRK2 mutation carriers.
Gorostidi A, Bergareche A, Ruiz-Martínez J, Martí-Massó JF, Cruz M, Varghese S, Qureshi MM, Alzahmi F, Al-Hayani A, López de Munáin A, El-Agnaf OM. Gorostidi A, et al. PLoS One. 2012;7(12):e52312. doi: 10.1371/journal.pone.0052312. Epub 2012 Dec 27. PLoS One. 2012. PMID: 23300640 Free PMC article.
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism.
Martí-Massó JF, Bergareche A, Makarov V, Ruiz-Martinez J, Gorostidi A, López de Munain A, Poza JJ, Striano P, Buxbaum JD, Paisán-Ruiz C. Martí-Massó JF, et al. Among authors: gorostidi a. J Mol Med (Berl). 2013 Dec;91(12):1399-406. doi: 10.1007/s00109-013-1075-4. Epub 2013 Aug 20. J Mol Med (Berl). 2013. PMID: 23955123 Free PMC article.
Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.
Ruiz-Martínez J, de la Riva P, Rodríguez-Oroz MC, Mondragón Rezola E, Bergareche A, Gorostidi A, Gago B, Estanga A, Larrañaga N, Sarasqueta C, López de Munain A, Martí Massó JF. Ruiz-Martínez J, et al. Among authors: gorostidi a. Mov Disord. 2014 May;29(6):750-5. doi: 10.1002/mds.25778. Epub 2013 Dec 19. Mov Disord. 2014. PMID: 24357540
Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2.
Estanga A, Rodriguez-Oroz MC, Ruiz-Martinez J, Barandiaran M, Gorostidi A, Bergareche A, Mondragon E, Lopez de Munain A, Marti-Masso JF. Estanga A, et al. Among authors: gorostidi a. Parkinsonism Relat Disord. 2014 Oct;20(10):1097-100. doi: 10.1016/j.parkreldis.2014.07.005. Epub 2014 Jul 30. Parkinsonism Relat Disord. 2014. PMID: 25127457
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy.
Bergareche A, Bednarz M, Sánchez E, Krebs CE, Ruiz-Martinez J, De La Riva P, Makarov V, Gorostidi A, Jurkat-Rott K, Marti-Masso JF, Paisán-Ruiz C. Bergareche A, et al. Among authors: gorostidi a. Hum Mol Genet. 2015 Dec 15;24(24):7111-20. doi: 10.1093/hmg/ddv410. Epub 2015 Oct 1. Hum Mol Genet. 2015. PMID: 26427606 Free PMC article.
105 results