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2015
De Leo L, Quaglia S, Ziberna F, Vatta S, Martelossi S, Maschio M, Not T. Serum anti-tissue transglutaminase antibodies detected during febrile illness may not be produced by the intestinal mucosa. J Pediatr 2015;166(3):761-3.
Morgan A, Gandin I, Belcaro C, Palumbo P, Palumbo O, Biamino E, Dal Col V, Laurini E, Pricl S, Bosco P, Carella M, Ferrero GBattista, Romano C, d'Adamo APio, Faletra F, Vozzi D. Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutat Res 2015;781:32-6.
Morgan A, Gandin I, Belcaro C, Palumbo P, Palumbo O, Biamino E, Dal Col V, Laurini E, Pricl S, Bosco P, Carella M, Ferrero GBattista, Romano C, d'Adamo APio, Faletra F, Vozzi D. Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutat Res 2015;781:32-6.
Tavares MCMansur, Júnior SF de Lima, Coelho AVC, Marques TRuschelle, de Araújo DHenrique T, Heráclio Sde A, Amorim MMRamos, de Souza PRoberto E, Crovella S. Tumor necrosis factor (TNF) alpha and interleukin (IL) 18 genes polymorphisms are correlated with susceptibility to HPV infection in patients with and without cervical intraepithelial lesion. Ann Hum Biol 2015;:1-8.
Tavares MCMansur, Júnior SF de Lima, Coelho AVC, Marques TRuschelle, de Araújo DHenrique T, Heráclio Sde A, Amorim MMRamos, de Souza PRoberto E, Crovella S. Tumor necrosis factor (TNF) alpha and interleukin (IL) 18 genes polymorphisms are correlated with susceptibility to HPV infection in patients with and without cervical intraepithelial lesion. Ann Hum Biol 2015;:1-8.
de Moura RR, Balbino Vde Queiroz, Crovella S, Brandão LAC. On the use of Chinese population as a proxy of Amerindian ancestors in genetic admixture studies with Latin American populations. Eur J Hum Genet 2015;
Lenarduzzi S, Vozzi D, Morgan A, Rubinato E, D'Eustacchio A, Osland TM, Rossi C, Graziano C, Castorina P, Ambrosetti U, Morgutti M, Girotto G. Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis. Hear Res 2015;320:18-23.
Cavalcanti CAddobbati, Silva JDe Azevêd, Pita Wde Barros, Veit TDegani, Monticielo OAndre, Xavier RMachado, Brenol JCarlos Tav, Brenol CViegas, Fragoso TSotero, Barbosa ADomingues, Duarte ÂLuiza Bran, Oliveira RDonizeti R, Louzada-Júnior P, Donadi EAntônio, Crovella S, Chies JArtur Bogo, Sandrin-Garcia P. Vitamin D receptor polymorphisms and expression profile in rheumatoid arthritis brazilian patients. Mol Biol Rep 2015;
Cavalcanti CAddobbati, Silva JDe Azevêd, Pita Wde Barros, Veit TDegani, Monticielo OAndre, Xavier RMachado, Brenol JCarlos Tav, Brenol CViegas, Fragoso TSotero, Barbosa ADomingues, Duarte ÂLuiza Bran, Oliveira RDonizeti R, Louzada-Júnior P, Donadi EAntônio, Crovella S, Chies JArtur Bogo, Sandrin-Garcia P. Vitamin D receptor polymorphisms and expression profile in rheumatoid arthritis brazilian patients. Mol Biol Rep 2015;
Travan L, Rocca MSanta, Buonomo F, Cleva L, Pecile V, De Cunto A. When Feeding Difficulties Are due to Genetics: The Case of Familial Partial 9q Duplication. J Investig Med High Impact Case Rep 2015;3(1):2324709615574949.
2014
Marzuillo P, Benettoni A, Germani C, Ferrara G, D'Agata B, Barbi E. Acquired long QT syndrome: a focus for the general pediatrician. Pediatr Emerg Care 2014;30(4):257-61.
Noris P, Schlegel N, Klersy C, Heller PG, Civaschi E, Pujol-Moix N, Fabris F, Favier R, Gresele P, Latger-Cannard V, Cuker A, Nurden P, Greinacher A, Cattaneo M, De Candia E, Pecci A, Hurtaud-Roux M-F, Glembotsky AC, Muñiz-Diaz E, Randi MLuigia, Trillot N, Bury L, Lecompte T, Marconi C, Savoia A, Balduini CL, Bayart S, Bauters A, Benabdallah-Guedira S, Boehlen F, Borg J-Y, Bottega R, Bussel J, De Rocco D, de Maistre E, Faleschini M, Falcinelli E, Ferrari S, Ferster A, Fierro T, Fleury D, Fontana P, James C, Lanza F, Duchez VLe Cam, Loffredo G, Magini P, Martin-Coignard D, Menard F, Mercier S, Mezzasoma A, Minuz P, Nichele I, Notarangelo LD, Pippucci T, Podda GMarco, Pouymayou C, Rigouzzo A, Royer B, Sie P, Siguret V, Trichet C, Tucci A, Saposnik B, Veneri D. Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia. Haematologica 2014;99(8):1387-94.

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