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Publicaciones - Investigación en Pediatría

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Crous-Bou M, De Vivo I, Porta M, Pumarega JA, López T, Alguacil J, Morales E, Malats N, Rifà J, Hunter DJ, Real FX; PANKRAS II Study Group. CYP1B1 polymorphisms and k-ras mutations in patients with pancreatic ductal adenocarcinoma. Dig Dis Sci. 2008 May;53(5):1417-21. doi: 10.1007/s10620-008-0235-9. Epub 2008 Mar 18. PubMed PMID: 18347981.
AÑO: 2008; IF: 1.583
García-Marcos L, Carvajal Urueña I, Escribano Montaner A, Fernández Benítez M, García de la Rubia S, Tauler Toro E, Pérez Fernández V, Barcina Sánchez C. Seasons and other factors affecting the quality of life of asthmatic children. J Investig Allergol Clin Immunol. 2007;17(4):249-56. PubMed PMID: 17694697.
AÑO: 2007; IF: 1.254
Clewing JM, Fryssira H, Goodman D, Smithson SF, Sloan EA, Lou S, Huang Y, Choi K, Lücke T, Alpay H, André JL, Asakura Y, Biebuyck-Gouge N, Bogdanovic R, Bonneau D, Cancrini C, Cochat P, Cockfield S, Collard L, Cordeiro I, Cormier-Daire V, Cransberg K, Cutka K, Deschenes G, Ehrich JH, Fründ S, Georgaki H, Guillen-Navarro E, Hinkelmann B, Kanariou M, Kasap B, Kilic SS, Lama G, Lamfers P, Loirat C, Majore S, Milford D, Morin D, Ozdemir N, Pontz BF, Proesmans W, Psoni S, Reichenbach H, Reif S, Rusu C, Saraiva JM, Sakallioglu O, Schmidt B, Shoemaker L, Sigaudy S, Smith G, Sotsiou F, Stajic N, Stein A, Stray-Pedersen A, Taha D, Taque S, Tizard J, Tsimaratos M, Wong NA, Boerkoel CF. Schimke immunoosseous dysplasia: suggestions of genetic diversity. Hum Mutat. 2007 Mar;28(3):273-83. PubMed PMID: 17089404.
AÑO: 2007; IF: 6.273
Garcia-Marcos L, Garcia-Hernández G, Morales Suarez-Varela M, Batlles Garrido J, Castro-Rodriguez JA. Asthma attributable to atopy: does it depend on the allergen supply? Pediatr Allergy Immunol. 2007 May;18(3):181-7. Epub 2007 Mar 7. Erratum in: Pediatr Allergy Immunol. 2007 Jun;18(4):368. PubMed PMID: 17346301.
AÑO: 2007; IF: 2.454
Ali A, Christie PT, Grigorieva IV, Harding B, Van Esch H, Ahmed SF, Bitner-Glindzicz M, Blind E, Bloch C, Christin P, Clayton P, Gecz J, Gilbert-Dussardier B, Guillen-Navarro E, Hackett A, Halac I, Hendy GN, Lalloo F, Mache CJ, Mughal Z, Ong AC, Rinat C, Shaw N, Smithson SF, Tolmie J, Weill J, Nesbit MA, Thakker RV. Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor. Hum Mol Genet. 2007 Feb 1;16(3):265-75. Epub 2007 Jan 8. PubMed PMID: 17210674.
AÑO: 2007; IF: 7.806
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Instituto de Investigación Sanitaria Acreditado

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