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2016
Zanella S, De Leo L, Nguyen-Ngoc-Quynh L, Nguyen-Duy B, Not T, Tran-Thi-Chi M, Phung-Duc S, Le-Thanh H, Malaventura C, Vatta S, Ziberna F, Mazzocco M, Volpato S, Phung-Tuyet L, Le-Thi-Minh H, Borgna-Pignatti C. Cross-sectional study of coeliac autoimmunity in a population of Vietnamese children. BMJ Open 2016;6(6):e011173.
Krauss BS, Calligaris L, Green SM, Barbi E. Current concepts in management of pain in children in the emergency department. Lancet 2016;387(10013):83-92.
2015
Tornese G, Marzuillo P, Pellegrin MChiara, Germani C, Faleschini E, Zennaro F, Grandone A, Del Giudice EMiraglia, Perrone L, Ventura A. A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood. Clin Endocrinol (Oxf) 2015;83(3):437-9.
Crocoli A, Tornesello A, Pittiruti M, Barone A, Muggeo P, Inserra A, Molinari AClaudio, Grillenzoni V, Durante V, Cicalese MPia, Zanazzo GAndrea, Cesaro S. Central venous access devices in pediatric malignancies: a position paper of Italian Association of Pediatric Hematology and Oncology. J Vasc Access 2015;16(2):130-6.
Bembich S, Travan L, Cont G, Bua J, Strajn T, Demarini S. Cerebral oxygenation with different nasal continuous positive airway pressure levels in preterm infants. Arch Dis Child Fetal Neonatal Ed 2015;100(2):F165-8.
Rusconi D, Negri G, Colapietro P, Picinelli C, Milani D, Spena S, Magnani C, Silengo MCirillo, Sorasio L, Curtisova V, Cavaliere MLuigia, Prontera P, Stangoni G, Ferrero GBattista, Biamino E, Fischetto R, Piccione M, Gasparini P, Salviati L, Selicorni A, Finelli P, Larizza L, Gervasini C. Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire. Hum Genet 2015;134(6):613-26.
Callea M, Yavuz I, Clarich G, Cammarata-Scalisi F. [Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2015;113(6):e341-4.
Nicchia E, Benedicenti F, De Rocco D, Greco C, Bottega R, Inzana F, Faleschini M, Bonin S, Cappelli E, Mogni M, Stanzial F, Svahn J, Dufour C, Savoia A. Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Birth Defects Res A Clin Mol Teratol 2015;103(12):1003-1010.
Benelli E, Carrato V, Martelossi S, Ronfani L, Not T, Ventura A. Coeliac disease in the ERA of the new ESPGHAN and BSPGHAN guidelines: a prospective cohort study. Arch Dis Child 2015;
Agostinis C, Zorzet S, De Leo R, Zauli G, De Seta F, Bulla R. The combination of N-acetyl cysteine, alpha-lipoic acid, and bromelain shows high anti-inflammatory properties in novel in vivo and in vitro models of endometriosis. Mediators Inflamm 2015;2015:918089.
Santarelli L, Staffolani S, Strafella E, Nocchi L, Manzella N, Grossi P, Bracci M, Pignotti E, Alleva R, Borghi B, Pompili C, Sabbatini A, Rubini C, Zuccatosta L, Bichisecchi E, Valentino M, Horwood K, Comar M, Bovenzi M, Dong L-F, Neuzil J, Amati M, Tomasetti M. Combined circulating epigenetic markers to improve mesothelin performance in the diagnosis of malignant mesothelioma. Lung Cancer 2015;
Monasta L, Knowles A. Comment on: 'Anthropometric parameters in relation to glycaemic status and lipid profile in a multi-ethnic sample in Italy' by Gualdi-Russo et al. Public Health Nutr 2015;:1.

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