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2015
Cani A, Simioni C, Martelli AM, Zauli G, Tabellini G, Ultimo S, McCubrey JA, Capitani S, Neri LM. Triple Akt inhibition as a new therapeutic strategy in T-cell acute lymphoblastic leukemia. Oncotarget 2015;6(9):6597-610.
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.
Maranhão RM de Albuq, Esteves FAMartins, Crovella S, Segat L, Souza PREleutér. Tumor necrosis factor-α and interleukin-6 gene polymorphism association with susceptibility to celiac disease in Italian patients. Genet Mol Res 2015;14(4):16343-52.
Ura B, Scrimin F, Zanconati F, Arrigoni G, Monasta L, Romano A, Banco R, Zweyer M, Milani D, Ricci G. Two-dimensional gel electrophoresis analysis of the leiomyoma interstitial fluid reveals altered protein expression with a possible involvement in pathogenesis. Oncol Rep 2015;33(5):2219-26.
Ura B, Scrimin F, Zanconati F, Arrigoni G, Monasta L, Romano A, Banco R, Zweyer M, Milani D, Ricci G. Two-dimensional gel electrophoresis analysis of the leiomyoma interstitial fluid reveals altered protein expression with a possible involvement in pathogenesis. Oncol Rep 2015;33(5):2219-26.
Bianco AMonica, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.
Ricci G, Andolfi L, Zabucchi G, Luppi S, Boscolo R, Martinelli M, Zweyer M, Trevisan E. Ultrastructural Morphology of Sperm from Human Globozoospermia. Biomed Res Int 2015;2015:798754.
Barrani M, Massei F, Scaglione M, Paolicchi A, Vitali S, Ciancia EM, Crovella S, Caparello MC, Consolini R. Unusual onset of a case of chronic recurrent multifocal osteomyelitis. Pediatr Rheumatol Online J 2015;13(1):60.
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.
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;
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.

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