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Unrelated donor marrow transplantation: An update of the experience of the Italian Bone Marrow Transplant Group (GITMO) 2000 Dini G.; Cancedda R.; Locatelli F.; Bosi A.; Bandini G.; Alessandrino E.P.; Porta F.; Uderzo C.; Messina C.; Fagioli F.; Arcese W.; Marenco P.; Fanin R.; Falda M.; Soligo D.; La Nasa G.; Giardini C.; Pession A.; Scime R.; Di Bartolomeo P.; Bruno B.; Garbarino L.; Lamparelli T.; Giorgiani G.; Lanino E.; Manzitti C.; Bacigalupo A.
[Congenital hypopituitarism in agenesis of the anterior pituitary gland: immediate management and follow-up]. 2006 Mussa A;Porta F;Baldassarre G;Corrias A;Bellone J;de Sanctis C
A COMPARISON BETWEEN SIMPLE PHE AND COMBINED PHE+BH4 LOADING TEST IN PHENYLKETONURIA 2006 PORTA F; ALLUTO A; MUSSA A; SPADA M; A. PONZONE
Bone alterations in children and young adults with renal transplant assessed by phalangeal quantitative ultrasound. 2007 Mussa, Alessandro; Porta, Francesco; Gianoglio, Bruno; Gaido, Maurizio; Nicolosi, Mario Guido; De Terlizzi, Francesca; de Sanctis, Carlo; Coppo, Rosanna
Riduzione dell'attività dell'arilsulfatasi B in pazienti affetti da fibrosi cistica 2007 Pagliardini S; Porta F; Bena C; Biamino E; Velijkovic A; Tardivo I; Bignamini E; Silengo M; Ferrero GB
Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria. 2008 Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency. 2008 Jäggi L; Zurflüh MR; Schuler A; Ponzone A; Porta F; Fiori L; Giovannini M; Santer R; Hoffmann GF; Ibel H; Wendel U; Ballhausen D; Baumgartner MR; Blau N.
In vivo specific reduction of arylsulfatase B enzymatic activity in children with cystic fibrosis 2008 FERRERO GB; PAGLIARDINI S; VELIJKOVIC A; PORTA F; BENA C; TARDIVO I; RESTAGNO G; CIRILLO M
Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study. 2008 Porta F; Spada M; Lala R; Mussa A.
Increased spontaneous osteoclastogenesis from peripheral blood mononuclear cells in phenylketonuria. 2008 Porta F; Roato I; Mussa A; Repici M; Gorassini E; Spada M; Ferracini R.
Dopamine agonists in 6-pyruvoyl tetrahydropterin synthase deficiency. 2009 Porta F; Mussa A; Concolino D; Spada M; Ponzone A.
In response to van Spronsen et al (2009) phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKU (J Inherit Metab Dis 32: 27-31). 2009 Ponzone A; Mussa A; Porta F.
Bone impairment in phenylketonuria is characterized by circulating osteoclast precursors and activated T cell increase. 2010 Roato I; Porta F; Mussa A; D'Amico L; Fiore L; Garelli D; Spada M; Ferracini R.
Fractures and skeletal complications should be the gold standard for validation of methods for bone appraisal in pediatrics 2010 Mussa A.; Bertorello N.; Porta F.; Galletto C.; Nicolosi M.G.; Manicone R.; Corrias A.; Fagioli F.
The overlap between Sotos and Beckwith-Wiedemann syndromes 2010 Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB.
Prospective bone ultrasound patterns during childhood acute lymphoblastic leukemia treatment. 2010 Mussa A; Bertorello N; Porta F; Galletto C; Nicolosi MG; Manicone R; Corrias A; Fagioli F.
Breastfeeding effects on newborn screening. 2010 Porta F; Mussa A; Ponzone A.
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency. 2010 Ponzone A; Porta F; Mussa A; Alluto A; Ferraris S; Spada M.
Bone quantitative ultrasound in congenital and acquired childhood multiple pituitary failure. 2010 Mussa A; Repici M; Fiore L; Tuli G; Porta F; Matarazzo P.
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency. 2010 Leuzzi V; Carducci CA; Carducci CL; Pozzessere S; Burlina A; Cerone R; Concolino D; Donati MA; Fiori L; Meli C; Ponzone A; Porta F; Strisciuglio P; Antonozzi I; Blau N.
Mostrati risultati da 1 a 20 di 54
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