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Caselli D, Petris MGrazia, Rondelli R, Carraro F, Colombini A, Muggeo P, Ziino O, Melchionda F, Russo G, Pierani P, Soncini E, DeSantis R, Zanazzo G, Barone A, Cesaro S, Cellini M, Mura R, Milano GM, Meazza C, Cicalese MP, Tropia S, De Masi S, Castagnola E, Aricò M. Single-day trimethoprim/sulfamethoxazole prophylaxis for Pneumocystis pneumonia in children with cancer. J Pediatr 2014;164(2):389-92.e1.
Mazzoni E, Rigolin GMatteo, Alaribe FNneka, Pancaldi C, Maniero S, Comar M, Martini F, Tognon M. Simian virus 40 efficiently infects human T lymphocytes and extends their lifespan. Exp Hematol 2012;40(6):466-76.
Lenarduzzi S, Morgutti M, Crovella S, Coiana A, Rosatelli MC. Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genet Mol Res 2014;13(4):9636-41.
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.
Pastore S, Paloni G, Caorsi R, Ronfani L, Taddio A, Lepore L. Serum amyloid protein A concentration in cryopyrin-associated periodic syndromes patients treated with interleukin-1 beta antagonist. Clin Exp Rheumatol 2014;32(4 Suppl 84):S63-6.
Kawanda L, Capobianco I, Starc M, Felipe D, Zanon D, Barbi E, Munkela N, Rodrigues V, Malundo L, Not T. Sedation with intranasal midazolam of Angolan children undergoing invasive procedures. Acta Paediatr 2012;101(7):e296-8.
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.
Chinetti V, Iossa S, Auletta G, Laria C, De Luca M, Di Leva F, Riccardi P, Giannini P, Gasparini P, Ciccodicola A, Marciano E, Franzè A. Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss. Int J Audiol 2010;49(4):326-31.
Wolber LE, Girotto G, Buniello A, Vuckovic D, Pirastu N, Lorente-Cánovas B, Rudan I, Hayward C, Polasek O, Ciullo M, Mangino M, Steves C, Concas MPina, Cocca M, Spector TD, Gasparini P, Steel KP, Williams FMK. Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. Hum Mol Genet 2014;23(23):6407-18.
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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.
Colombo EA, Locatelli A, Sánchez LCubells, Romeo S, Elcioglu NH, Maystadt I, Martínez AEsteve, Sironi A, Fontana L, Finelli P, Gervasini C, Pecile V, Larizza L. Rothmund-Thomson Syndrome: Insights from New Patients on the Genetic Variability Underpinning Clinical Presentation and Cancer Outcome. Int J Mol Sci 2018;19(4)
Maximova N, Zanon D, Rovere F, Maestro A, Schillani G, Paparazzo R. Romiplostim for secondary thrombocytopenia following allogeneic stem cell transplantation in children. Int J Hematol 2015;102(5):626-32.

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