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Farruggia P, Fioredda F, Puccio G, Onofrillo D, Russo G, Barone A, Bonanomi S, Boscarol G, Finocchi A, Ghilardi R, Giordano P, Ladogana S, Lassandro G, Luti L, Lanza T, Mandaglio R, Marra N, Martire B, Mastrodicasa E, Motta M, Notarangelo LDora, Pillon M, Porretti L, Serafinelli J, Trizzino A, Tucci F, Veltroni M, Verzegnassi F, Ramenghi U, Dufour C. Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry. Am J Hematol 2019;94(2):216-222.
Ura B, Scrimin F, Franchin C, Arrigoni G, Licastro D, Monasta L, Ricci G. Identification of proteins with different abundance associated with cell migration and proliferation in leiomyoma interstitial fluid by proteomics. Oncol Lett 2017;13(5):3912-3920.
Callea M, Willoughby CE, Nieminen P, Di Stazio M, Bellacchio E, Giglio S, Sani I, Vinciguerra A, Maglione M, Tadini G, Clarich G. Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia. J Eur Acad Dermatol Venereol 2015;29(5):1032-4.
Athanasakis E, Biarnés X, Bonati MT, Gasparini P, Faletra F. Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome. Mol Syndromol 2012;3(1):21-24.
Chiurco A, Montico M, Brovedani P, Monasta L, Davanzo R. An IBCLC in the Maternity Ward of a Mother and Child Hospital: A Pre- and Post-Intervention Study. Int J Environ Res Public Health 2015;12(8):9938-51.

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