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SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation.
Fernández-Cancio M, Audí L, Andaluz P, Torán N, Piró C, Albisu M, Gussinyé M, Yeste D, Clemente M, Martínez-Mora J, Blanco A, Granada ML, Marco M, Ferragut J, López-Siguero JP, Beneyto M, Carles C, Carrascosa A. Fernández-Cancio M, et al. Among authors: marco m. Int J Androl. 2011 Dec;34(6 Pt 2):e526-35. doi: 10.1111/j.1365-2605.2010.01136.x. Epub 2011 Jun 2. Int J Androl. 2011. PMID: 21631525
Putative association of a mutant ROM1 allele with retinitis pigmentosa.
Martínez-Mir A, Vilela C, Bayés M, Valverde D, Dain L, Beneyto M, Marco M, Baiget M, Grinberg D, Balcells S, Gonzàlez-Duarte R, Vilageliu L. Martínez-Mir A, et al. Among authors: marco m. Hum Genet. 1997 Jun;99(6):827-30. doi: 10.1007/s004390050456. Hum Genet. 1997. PMID: 9187681 Free article.
[Multiple sclerosis epidemiological situation update: pertinence and set-up of a population based registry of new cases in Catalonia].
Otero S, Batlle J, Bonaventura I, Brieva L, Bufill E, Cano A, Carmona O, Escartín A, Marco M, Moral E, Munteis E, Nos C, Pericot I, Perkal H, Ramió-Torrentà L, Ramo-Tello C, Saiz A, Sastre-Garriga J, Tintoré M, Vaqué J, Montalban X; Grupo de Trabajo del Registro de Esclerosis Múltiple de Cataluña. Otero S, et al. Among authors: marco m. Rev Neurol. 2010 May 16;50(10):623-33. Rev Neurol. 2010. PMID: 20473839 Free article. Spanish.
[Otalgia as form of presentation of uncal herniation].
Peña-Segura JL, Marco M, Medrano P, Galván M, Abenia P, López-Pisón J. Peña-Segura JL, et al. Among authors: marco m. Rev Neurol. 2000 Nov 1-15;31(9):898-9. Rev Neurol. 2000. PMID: 11127098 Spanish. No abstract available.
Evaluation of cerebral function after carotid endarterectomy.
Uclés P, Almárcegui C, Lorente S, Romero F, Marco M. Uclés P, et al. Among authors: marco m. J Clin Neurophysiol. 1997 May;14(3):242-9. doi: 10.1097/00004691-199705000-00010. J Clin Neurophysiol. 1997. PMID: 9244165 Clinical Trial.
1,312 results