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Martínez-Lage JF, Guillén-Navarro E, López-Guerrero AL, Almagro MJ, Cuartero-Pérez B, de la Rosa P. Chiari type 1 anomaly in pseudohypoparathyroidism type Ia: pathogenetic hypothesis. Childs Nerv Syst. 2011 Dec;27(12):2035-9. doi: 10.1007/s00381-011-1606-7. Epub 2011 Oct 13. PubMed PMID: 21994050.
AÑO: 2011; IF: 1.542
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21994050
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Vera-Carbonell A, Moya-Quiles MR, Ballesta-Martínez M, López-González V, Bafallíu JA, Guillén-Navarro E, López-Expósito I. Rapp-Hodgkin syndrome and SHFM1 patients: delineating the p63-Dlx5/Dlx6 pathway. Gene. 2012 Apr 15;497(2):292-7. doi: 10.1016/j.gene.2012.01.088. Epub 2012 Feb 9. PubMed PMID: 22342398.
AÑO: 2012; IF: 2.196
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Puig-Hervás MT, Temtamy S, Aglan M, Valencia M, Martínez-Glez V, Ballesta-Martínez MJ, López-González V, Ashour AM, Amr K, Pulido V, Guillén-Navarro E, Lapunzina P, Caparrós-Martín JA, Ruiz-Perez VL. Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome--osteogenesis imperfecta phenotypic spectrum. Hum Mutat. 2012 Oct;33(10):1444-9. doi: 10.1002/humu.22133. Epub 2012 Jul 5. PubMed PMID: 22689593.
AÑO: 2012; IF: 5.213
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Sabater-Molina M, Guillén-Navarro E, García-Molina E, Ballesta-Martínez MJ, Escudero F, Ruiz-Espejo F. Barth syndrome in adulthood: a clinical case. Rev Esp Cardiol (Engl Ed). 2013 Jan;66(1):68-70. doi: 10.1016/j.recesp.2012.05.015. English, Spanish. PubMed PMID: 22999963.
AÑO: 2013; IF: 3.342
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de la Morena-Barrio ME, Hernández-Caselles T, Corral J, García-López R, Martínez-Martínez I, Pérez-Dueñas B, Altisent C, Sevivas T, Kristensen SR, Guillén-Navarro E, Miñano A, Vicente V, Jaeken J, Lozano ML. GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients. Orphanet J Rare Dis. 2013 Oct 20;8:170. doi: 10.1186/1750-1172-8-170. PubMed PMID: 24139637; PubMed Central PMCID: PMC4016514.
AÑO: 2013; IF: 4.123
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