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Medicina molecular

The p53 Codon 72 Polymorphism (rs1042522) Is Associated with Proliferative Vitreoretinopathy The Retina 4 Project
Pastor-Idoate S; Irene Rodríguez Hernández; Rojas J; Fernández I; García-Gutierrez MT; Ruiz-Moreno JM; Rocha-Sousa A; Ramkissoon Y; Harsum S; Maclaren RE; Charteris D; van Meurs J; Rogelio González Sarmiento; Pastor JC
Ophthalmology ; 120, pp. 623 - 628
PubMed
Enhanced immunological response by dendritic cells in male hypogonadism
Juan José Corrales Hernández; Maria Almeida; Mar Cordero; María Lourdes Martín Martín; Cristina Mendez; José Manuel Miralles García; Jose Alberto Orfao De Matos Correia e Vale
European Journal Of Clinical Investigation ; 42, pp. 1205 - 1212
PubMed
Prognostic value of telomere length in acute coronary syndrome
José Ángel Pérez Rivera; Pedro Pabon Osuna; Clara Cieza Borrella; Francisco Martín Herrero; José Ramón González Porras; Rogelio González Sarmiento
Mechanisms Of Ageing And Development ; 133, pp. 695 - 697
PubMed
Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain
Hernández-Martín A; Garcia-Doval I; Aranegui B; Pablo Unamuno Pérez; Rodríguez-Pazos L; González-Enseñat MA; Vicente A; Martín-Santiago A; Garcia-Bravo B; Feito M; Baselga E; Círia S; de Lucas R; Ginarte M; Rogelio González Sarmiento; Torrelo A
Journal Of The American Academy Of Dermatology ; 67, pp. 240 - 244
PubMed
Analysis of TRPV1 gene polymorphisms in Spanish patients with neuropathic pain
Pilar Armero; Clemente Muriel Villoria; Monica Lopez; Juan Santos; Rogelio González Sarmiento
Medicina Clinica ; 139, pp. 1 - 4
Association of mu-opioid receptor (OPRM1) gene polymorphism with response to naltrexone in alcohol dependence: a systematic review and meta-analysis
Chamorro AJ; Miguel Marcos Martín; José Antonio Mirón Canelo; Isabel Julia Pastor Encinas; Rogelio González Sarmiento; Francisco Javier Laso Guzmán
Addiction Biology ; 17, pp. 505 - 512
PubMed
Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases
Martinez-Delgado B; Yanowsky K; Inglada-Perez L; de la Hoya M; Caldes T; Vega A; Blanco A; Teresa Martín Gómez; Rogelio González Sarmiento; Blasco M; Robledo M; Urioste M; Song H; Pharoah P; Benitez J
Journal Of Medical Genetics ; 49, pp. 341 - 344
PubMed
Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hunermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature
Javier Cañueto Álvarez; Girós M; Ciria S; Pi-Castán G; Artigas M; García-Dorado J; García-Patos V; Virós A; Vendrell T; Torrelo A; Hernández-Martín A; Martín-Hernández E; Garcia-Silva MT; Fernández-Burriel M; Rosell J; Tejedor M; Martínez F; Luis Felix Valero Juan; Juan Luis García Hernández; Eva María Sánchez Tapia; Pablo Unamuno Pérez; Rogelio González Sarmiento
British Journal Of Dermatology ; 166, pp. 830 - 838
PubMed
Cannabinoid Receptor 1 Gene is Associated with Alcohol Dependence
Miguel Marcos Martín; Isabel Julia Pastor Encinas; Cristina de la Calle Cabrera; Barrio-Real L; Francisco Javier Laso Guzmán; Rogelio González Sarmiento
Alcoholism-Clinical And Experimental Research ; 36, pp. 267 - 271
PubMed
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: Identification a cryptic donor splice site in the exon 19
Targovnik HM; Edouard T; Varela V; Tauber M; Citterio CE; Rogelio González Sarmiento; Rivolta CM
Molecular And Cellular Endocrinology ; 348, pp. 313 - 321
PubMed

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