Export 1075 results:
Autore Titolo Tipo [ Anno(Desc)]
Filtri: First Letter Of Last Name è G  [Clear All Filters]
2015
Giordano P, Saracco P, Grassi M, Luciani M, Banov L, Carraro F, Crocoli A, Cesaro S, Zanazzo GAndrea, Molinari AClaudio. Recommendations for the use of long-term central venous catheter (CVC) in children with hemato-oncological disorders: management of CVC-related occlusion and CVC-related thrombosis. On behalf of the coagulation defects working group and the supportive the. Ann Hematol 2015;94(11):1765-76.
Masat E, Gasparini C, Agostinis C, Bossi F, Radillo O, De Seta F, Tamassia N, Cassatella MA, Bulla R. RelB activation in anti-inflammatory decidual endothelial cells: a master plan to avoid pregnancy failure?. Sci Rep 2015;5:14847.
Franca R, Stocco G, Favretto D, Giurici N, Decorti G, Rabusin M. Role of Pharmacogenetics in Hematopoietic Stem Cell Transplantation Outcome in Children. Int J Mol Sci 2015;16(8):18601-27.
Copertino M, Benelli E, Gregori M, Barbi E, Ventura A. A Shining Scrotal Fountain. J Pediatr 2015;167(1):205.e1.
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.
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.
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.
Perri P, Zauli G, Gonelli A, Milani D, Celeghini C, Lamberti G, Secchiero P. TNF-related apoptosis inducing ligand in ocular cancers and ocular diabetic complications. Biomed Res Int 2015;2015:424019.
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.
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.
Pascazio L, Bembich S, Nardone IB, Vecchiet C, Guarino G, Clarici A. Validation of the Italian translation of the affective neuroscience personality scales. Psychol Rep 2015;116(1):97-115.

Amministrazione Trasparente