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2015
Addobbati CJC, J Silva deAzevêdo, Tavares NAC, Araujo J, Guimarães RL, Brandão L, Crovella S, Sandrin-Garcia P. Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III. Genet Mol Res 2015;14(1):29-33.
Minute M, Patti G, Tornese G, Faleschini E, Zuiani C, Ventura A. Sirolimus Therapy in Congenital Hyperinsulinism: A Successful Experience Beyond Infancy. Pediatrics 2015;136(5):e1373-6.
Capolla S, Garrovo C, Zorzet S, Lorenzon A, Rampazzo E, Spretz R, Pozzato G, Núñez L, Tripodo C, Macor P, Biffi S. Targeted tumor imaging of anti-CD20-polymeric nanoparticles developed for the diagnosis of B-cell malignancies. Int J Nanomedicine 2015;10:4099-109.
Magnolato A, Pederiva F, Spagnut G, Maschio M, Ventura A, Taddio A. Three cases of Bartonella quintana infection in children. Pediatr Infect Dis J 2015;34(5):540-2.
Marcuzzi A, Piscianz E, Valencic E, Monasta L, Brumatti LVecchi, Tommasini A. To Extinguish the Fire from Outside the Cell or to Shutdown the Gas Valve Inside? Novel Trends in Anti-Inflammatory Therapies. Int J Mol Sci 2015;16(9):21277-93.
Rabelo KCN, Albuquerque CMR, Tavares VB, Santos SM, Souza CA, Oliveira TC, Oliveira NCL, Crovella S. Trace samples of human blood in mosquitoes as a forensic investigation tool. Genet Mol Res 2015;14(4):14847-56.
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.
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.
Frausin S, Viventi S, Falzacappa LVerga, Quattromani MJlenia, Leanza G, Tommasini A, Valencic E. Wharton's jelly derived mesenchymal stromal cells: Biological properties, induction of neuronal phenotype and current applications in neurodegeneration research. Acta Histochem 2015;117(4-5):329-38.
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.

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