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Tornese G, Tisato V, Monasta L, Brumatti LVecchi, Zauli G, Secchiero P. Serum TRAIL levels increase shortly after insulin therapy and metabolic stabilization in children with type 1 diabetes mellitus. Acta Diabetol 2015;52(5):1003-6.
Tornese G, Tonini G, Ventura A. Slow growth: do not forget the thyroid. J Pediatr Gastroenterol Nutr 2012;54(3):438; author reply 438.
Tornese G, Faleschini E, Matarazzo L, Bibalo C, Zanazzo GAndrea, Rabusin M, Tonini G, Zennaro F, Ventura A. Relapse and metastasis of atypical teratoid/rhabdoid tumor in a boy with neurofibromatosis type 1 treated with recombinant human growth hormone. Neuropediatrics 2015;46(2):126-9.
Tornese G, Ronfani L, Pavan C, Demarini S, Monasta L, Davanzo R. Does the LATCH score assessed in the first 24 hours after delivery predict non-exclusive breastfeeding at hospital discharge?. Breastfeed Med 2012;7(6):423-30.
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.
Toson B, Santos EJosé Dos, Adelino JEduardo, Sandrin-Garcia P, Crovella S, Louzada-Júnior P, Oliveira RDonizete R, Pedroza LSanta Rosa, Sauma Mde Fátima, de Lima CPereira Si, Barbosa FBrasil, Brenol CViegas, Xavier RMachado, Chies JArtur Bogo, Veit TDegani. CCR5Δ32 and the genetic susceptibility to rheumatoid arthritis in admixed populations: a multicentre study. Rheumatology (Oxford) 2017;56(3):495-497.
Trapella C, Voltan R, Melloni E, Tisato V, Celeghini C, Bianco S, Fantinati A, Salvadori S, Guerrini R, Secchiero P, Zauli G. Design, Synthesis, and Biological Characterization of Novel Mitochondria Targeted Dichloroacetate-Loaded Compounds with Antileukemic Activity. J Med Chem 2015;
Travan L, Lega S, Crovella S, Montico M, Panontin E, Demarini S. Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism. J Pediatr 2014;165(1):42-5.
Travan L, Rocca MSanta, Buonomo F, Cleva L, Pecile V, De Cunto A. When Feeding Difficulties Are due to Genetics: The Case of Familial Partial 9q Duplication. J Investig Med High Impact Case Rep 2015;3(1):2324709615574949.
Travan L, Naviglio S, Cont G, Brovedani P, Davanzo R, Demarini S. Isolated hypoplasia of abdominal wall muscles associated with fetal ascites. Congenit Anom (Kyoto) 2016;56(4):184-186.
Travan L, Naviglio S, De Cunto A, Pellegrin A, Pecile V, Spinelli AMauro, Cappellani S, Faletra F. Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literature. Am J Med Genet A 2017;
Travan L, Demarini S, Del Frate G, Zacchi A. Congenital hemangiopericytoma. J Pediatr 2012;160(5):878.

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