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Publicaciones - Investigación en Pediatría

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Mitchell EA, Clayton T, García-Marcos L, Pearce N, Foliaki S, Wong G; ISAAC Phase Three Study Group.. Birthweight and the risk of atopic diseases: the ISAAC Phase III study. Pediatr Allergy Immunol. 2014 May;25(3):264-70. doi: 10.1111/pai.12233_1. PubMed PMID: 24750571.
AÑO: 2014; IF: 3.397
Alfayate-Miguélez S, Ruiz-Gómez J, Fenoll-Comes A, Sanchez-Solis-de Querol M, Iofrío-de Arce A, Casquet-Barceló A, Sanz-Mateo G, Espejo-García P, Lorente-García S, Sánchez-Andrada RM, Vigueras-Abellán JJ; Grupo de estudio de Enfermedades infecciosas de la comunidad autónoma de Murcia.. [Epidemiological study of nasopharyngeal carriers of Streptococcus pneumoniae in children in Murcia region]. Enferm Infecc Microbiol Clin. 2014 Aug-Sep;32(7):434-40. doi: 10.1016/j.eimc.2013.07.013. Spanish. PubMed PMID: 25034854.
AÑO: 2014; IF: 2.172
Martinez-Cayuelas E, Herraiz-Martinez M, Villacieros-Hernandez L, Cean-Cabrera L, Martinez-Salcedo E, Alarcon-Martinez H, Domingo-Jimenez R, Perez-Fernandez V. [Complex febrile crises: should we change the way we act?]. Rev Neurol. 2014 Nov 16;59(10):449-58. Spanish. PubMed PMID: 25354507.
AÑO: 2014; IF: 0.83
McKee M, Haines A, Ebrahim S, Lamptey P, Barreto ML, Matheson D, Walls HL, Foliaki S, Miranda JJ, Chimeddamba O, Garcia-Marcos L, Vineis P, Pearce N. Towards a comprehensive global approach to prevention and control of NCDs. Global Health. 2014 Oct 28;10:74. doi: 10.1186/s12992-014-0074-8. PubMed PMID: 25348262; PubMed Central PMCID: PMC4215019.
AÑO: 2014; IF: 2.25
Kaiser FJ, Ansari M, Braunholz D, Concepción Gil-Rodríguez M, Decroos C, Wilde JJ, Fincher CT, Kaur M, Bando M, Amor DJ, Atwal PS, Bahlo M, Bowman CM, Bradley JJ, Brunner HG, Clark D, Del Campo M, Di Donato N, Diakumis P, Dubbs H, Dyment DA, Eckhold J, Ernst S, Ferreira JC, Francey LJ, Gehlken U, Guillén-Navarro E, Gyftodimou Y, Hall BD, Hennekam R, Hudgins L, Hullings M, Hunter JM, Yntema H, Innes AM, Kline AD, Krumina Z, Lee H, Leppig K, Lynch SA, Mallozzi MB, Mannini L, McKee S, Mehta SG, Micule I; Care4Rare Canada Consortium., Mohammed S, Moran E, Mortier GR, Moser JA, Noon SE, Nozaki N, Nunes L, Pappas JG, Penney LS, Pérez-Aytés A, Petersen MB, Puisac B, Revencu N, Roeder E, Saitta S, Scheuerle AE, Schindeler KL, Siu VM, Stark Z, Strom SP, Thiese H, Vater I, Willems P, Williamson K, Wilson LC; University of Washington Center for Mendelian Genomics., Hakonarson H, Quintero-Rivera F, Wierzba J, Musio A, Gillessen-Kaesbach G, Ramos FJ, Jackson LG, Shirahige K, Pié J, Christianson DW, Krantz ID, Fitzpatrick DR, Deardorff MA. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Hum Mol Genet. 2014 Jun 1;23(11):2888-900. doi: 10.1093/hmg/ddu002. PubMed PMID: 24403048; PubMed Central PMCID: PMC4014191.
AÑO: 2014; IF: 6.393
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