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2015
Habtamu HB, Sentic M, Silvestrini M, De Leo L, Not T, Arbault S, Manojlovic D, Sojic N, Ugo P. A Sensitive Electrochemiluminescence Immunosensor for Celiac Disease Diagnosis Based on Nanoelectrode Ensembles. Anal Chem 2015;87(24):12080-7.
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.
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.
Naviglio S, Abate MValentina, Chinello M, Ventura A. Splenic Infarction in Acute Infectious Mononucleosis. J Emerg Med 2015;
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.
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.
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.
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.
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.

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