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Faletra F, d'Adamo APio, Pensiero S, Athanasakis E, Catalano D, Bruno I, Gasparini P. A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family. Ophthalmic Genet 2013;34(1-2):115-7.
Faletra F, Girotto G, d'Adamo APio, Vozzi D, Morgan A, Gasparini P. A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss. Gene 2014;534(2):236-9.
Faletra F, d'Adamo APio, Rocca MSanta, Carrozzi M, Perrone MDolores, Pecile V, Gasparini P. Does the 1.5 Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature. Am J Med Genet A 2012;158A(2):461-4.
Faletra F, Berti I, Tommasini A, Pecile V, Cleva L, Alberini E, Bruno I, Gasparini P. Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis. Dermatology 2012;225(4):294-7.
Faletra F, Devescovi R, Pecile V, Fabretto A, Carrozzi M, Gasparini P. A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature. J Appl Genet 2011;52(1):77-80.
Fanfani F, Monterossi G, Fagotti A, Gallotta V, Costantini B, Vizzielli G, Petrillo M, Carbone MVittoria, Scambia G. Positron emission tomography-laparoscopy based method in the prediction of complete cytoreduction in platinum-sensitive recurrent ovarian cancer. Ann Surg Oncol 2015;22(2):649-54.
Fanfani F, Restaino S, Cicogna S, Petrillo M, Montico M, Perrone E, Radillo O, De Leo R, Ceccarello M, Scambia G, Ricci G. Preoperative Serum Human Epididymis Protein 4 Levels in Early Stage Endometrial Cancer: A Prospective Study. Int J Gynecol Cancer 2017;27(6):1200-1205.
Faraci M, Zecca M, Pillon M, Rovelli A, Menconi MCristina, Ripaldi M, Fagioli F, Rabusin M, Ziino O, Lanino E, Locatelli F, Daikeler T, Prete A. Autoimmune hematological diseases after allogeneic hematopoietic stem cell transplantation in children: an Italian multicenter experience. Biol Blood Marrow Transplant 2014;20(2):272-8.
Farchi S, Forastiere F, Brumatti LVecchi, Alviti S, Arnofi A, Bernardini T, Bin M, Brescianini S, Colelli V, Cotichini R, Culasso M, De Bartolo P, Felice L, Fiano V, Fioritto A, Frizzi A, Gagliardi L, Giorgi G, Grasso C, La Rosa F, Loganes C, Lorusso P, Martini V, Merletti F, Medda E, Montelatici V, Mugelli I, Narduzzi S, Nisticò L, Penna L, Piscianz E, Piscicelli C, Poggesi G, Porta D, Ranieli A, Rapisardi G, Rasulo A, Richiardi L, Rusconi F, Serino L, Stazi MAntonietta, Toccaceli V, Todros T, Tognin V, Trevisan M, Valencic E, Volpi P, Ziroli V, Ronfani L, Di Lallo D. Piccolipiù, a multicenter birth cohort in Italy: protocol of the study. BMC Pediatr 2014;14:36.
Farchi S, Ronfani L. [Breastfeeding in the first months of life: data from the "Piccolipiù" cohorts]. Epidemiol Prev 2015;39(5-6):392.
Färkkilä A, Zauli G, Haltia U-M, Pihlajoki M, Unkila-Kallio L, Secchiero P, Heikinheimo M. Circulating levels of TNF-related apoptosis inducing-ligand are decreased in patients with large adult-type granulosa cell tumors-implications for therapeutic potential. Tumour Biol 2016;
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.

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