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Conter V, Valsecchi MGrazia, Parasole R, Putti MCaterina, Locatelli F, Barisone E, Nigro LLo, Santoro N, Aricò M, Ziino O, Pession A, Testi AMaria, Micalizzi C, Casale F, Zecca M, Casazza G, Tamaro P, La Barba G, Notarangelo LDora, Silvestri D, Colombini A, Rizzari C, Biondi A, Masera G, Basso G. Childhood high-risk acute lymphoblastic leukemia in first remission: results after chemotherapy or transplant from the AIEOP ALL 2000 study. Blood 2014;123(10):1470-8.
Conter V, Valsecchi MGrazia, Parasole R, Putti MCaterina, Locatelli F, Barisone E, Nigro LLo, Santoro N, Aricò M, Ziino O, Pession A, Testi AMaria, Micalizzi C, Casale F, Zecca M, Casazza G, Tamaro P, La Barba G, Notarangelo LDora, Silvestri D, Colombini A, Rizzari C, Biondi A, Masera G, Basso G. Childhood high-risk acute lymphoblastic leukemia in first remission: results after chemotherapy or transplant from the AIEOP ALL 2000 study. Blood 2014;123(10):1470-8.
Pastore S, Ferrara G, Monasta L, Meini A, Cattalini M, Martino S, Alessio M, La Torre F, Teruzzi B, Gerloni V, Breda L, Taddio A, Lepore L. Chronic nonbacterial osteomyelitis may be associated with renal disease and bisphosphonates are a good option for the majority of patients. Acta Paediatr 2016;105(7):e328-33.
Pastore S, Ferrara G, Monasta L, Meini A, Cattalini M, Martino S, Alessio M, La Torre F, Teruzzi B, Gerloni V, Breda L, Taddio A, Lepore L. Chronic nonbacterial osteomyelitis may be associated with renal disease and bisphosphonates are a good option for the majority of patients. Acta Paediatr 2016;105(7):e328-33.
Corallini F, Secchiero P, Castellino G, Montecucco M, Trotta F, Zauli G. Circulating levels of frizzled-related protein (FRZB) are increased in patients with early rheumatoid arthritis and decrease in response to disease-modifying antirheumatic drugs. Ann Rheum Dis 2010;69(9):1733-4.
Bernardi S, Toffoli B, Bossi F, Candido R, Stenner E, Carretta R, Barbone F, Fabris B. Circulating osteoprotegerin is associated with chronic kidney disease in hypertensive patients. BMC Nephrol 2017;18(1):219.
Chermetz M, Gobbo M, Ronfani L, Ottaviani G, Zanazzo GA, Verzegnassi F, Treister NS, Di Lenarda R, Biasotto M, Zacchigna S. Class IV laser therapy as treatment for chemotherapy-induced oral mucositis in onco-haematological paediatric patients: a prospective study. Int J Paediatr Dent 2014;24(6):441-9.
Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
Naselli A, Penco F, Cantarini L, Insalaco A, Alessio M, Tommasini A, Maggio C, Obici L, Gallizi R, Cimmino M, Signa S, Lucherini OMaria, Carta S, Caroli F, Martini A, Rubartelli A, Ceccherini I, Gattorno M. Clinical Characteristics of Patients Carrying the Q703K Variant of the NLRP3 Gene: A 10-year Multicentric National Study. J Rheumatol 2016;43(6):1093-100.
Cancrini C, Puliafito P, Digilio MCristina, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EMaria, Cardinale F, Finocchi A, Romiti MLuisa, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MCristina, Marino B, Ugazio AGiovanni, Plebani A, Rossi P. Clinical features and follow-up in patients with 22q11.2 deletion syndrome. J Pediatr 2014;164(6):1475-80.e2.
Mazza C, Buzi F, Ortolani F, Vitali A, Notarangelo LD, Weber G, Bacchetta R, Soresina A, Lougaris V, Greggio NA, Taddio A, Pasic S, de Vroede M, Pac M, Kilic SSebnem, Ozden S, Rusconi R, Martino S, Capalbo D, Salerno M, Pignata C, Radetti G, Maggiore G, Plebani A, Notarangelo LD, Badolato R. Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. Clin Immunol 2011;139(1):6-11.

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