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2011
De Seta F, Banco R, Guaschino S, De Santo D, Turrisi A, Piva C. [Proteomic applications in gynecology-obstetrics]. Minerva Ginecol 2011;63(1):39-46.
Pastore S, Londero M, Cont G, Di Leo G, Ventura A. Refractory iron-deficiency anaemia in a child with portal cavernoma. Gut 2011;60(3):317, 377.
Pastore S, De Cunto A, Benettoni A, Berton E, Taddio A, Lepore L. The resurgence of rheumatic fever in a developed country area: the role of echocardiography. Rheumatology (Oxford) 2011;50(2):396-400.
da Silva RCelerino, Segat L, Crovella S. Role of DC-SIGN and L-SIGN receptors in HIV-1 vertical transmission. Hum Immunol 2011;72(4):305-11.
da Silva GKniphoff, Guimarães R, Mattevi VSuñé, Lazzaretti RKuhmmer, Sprinz E, Kuhmmer R, Brandão L, Crovella S, Chies JArtur Bogo. The role of mannose-binding lectin gene polymorphisms in susceptibility to HIV-1 infection in Southern Brazilian patients. AIDS 2011;25(4):411-8.
Floridia M, Pinnetti C, Ravizza M, Tibaldi C, Sansone M, Fiscon M, Guaraldi G, Guerra B, Alberico S, Spinillo A, Castelli P, Dalzero S, Cavaliere AFranca, Tamburrini E. Rubella susceptibility profile in pregnant women with HIV. Clin Infect Dis 2011;52(7):960-2.
De Cunto A, Barbi E, Minen F, Ventura A. Safety and efficacy of high-dose acarbose treatment for dumping syndrome. J Pediatr Gastroenterol Nutr 2011;53(1):113-4.
Comar M, Zanotta N, Rossi T, Pelos G, D'Agaro P. Secondary lymphoid tissue as an important site for WU polyomavirus infection in immunocompetent children. J Med Virol 2011;83(8):1446-50.
Rudan I, Arifeen SEl, Bhutta ZA, Black RE, Brooks A, Chan KYee, Chopra M, Duke T, Marsh D, Pio A, Simoes EAF, Tamburlini G, Theodoratou E, Weber MW, Whitney CG, Campbell H, Qazi SA. Setting research priorities to reduce global mortality from childhood pneumonia by 2015. PLoS Med 2011;8(9):e1001099.
Gana S, Sainati L, Frau MR, Monciotti C, Poli F, Cannioto Z, Comelli M, Danesino C, Minelli A. Shwachman-Diamond syndrome and type 1 diabetes mellitus: more than a chance association?. Exp Clin Endocrinol Diabetes 2011;119(10):610-2.
Pansuriya TC, van Eijk R, d'Adamo P, van Ruler MAJH, Kuijjer ML, Oosting J, Cleton-Jansen A-M, van Oosterwijk JG, Verbeke SLJ, Meijer D, van Wezel T, Nord KH, Sangiorgi L, Toker B, Liegl-Atzwanger B, San-Julian M, Sciot R, Limaye N, Kindblom L-G, Daugaard S, Godfraind C, Boon LM, Vikkula M, Kurek KC, Szuhai K, French PJ, Bovée JVMG. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet 2011;43(12):1256-61.
Pansuriya TC, van Eijk R, d'Adamo P, van Ruler MAJH, Kuijjer ML, Oosting J, Cleton-Jansen A-M, van Oosterwijk JG, Verbeke SLJ, Meijer D, van Wezel T, Nord KH, Sangiorgi L, Toker B, Liegl-Atzwanger B, San-Julian M, Sciot R, Limaye N, Kindblom L-G, Daugaard S, Godfraind C, Boon LM, Vikkula M, Kurek KC, Szuhai K, French PJ, Bovée JVMG. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet 2011;43(12):1256-61.

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