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Titolo Data di pubblicazione Autore(i) File
A COMPARISON BETWEEN SIMPLE PHE AND COMBINED PHE+BH4 LOADING TEST IN PHENYLKETONURIA 2006 PORTA F; ALLUTO A; MUSSA A; SPADA M; A. PONZONE
[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
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
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
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.
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.
Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria. 2008 Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
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.
Remittent hyperammonemia in congenital portosystemic shunt 2010 Ferrero GB; Porta F; Biamino E; Mussa A; Garelli E; Chiappe F; Veltri A; Silengo MC; Gennari F
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.
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.
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.
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.
Lysosomal enzyme activities in phenylketonuria. 2011 Porta F; Pagliardini S; Pagliardini V; Dotta A; Mussa A; Spada M.
Phenotyping and treatment of phenylketonuria. 2011 Porta F; Mussa A; Garelli D; Spada M.
Determinants of thyrotropin rise in congenital hypothyroidism 2011 Alessandro Mussa;Francesco Porta; Giuseppina Baldassarre; Andrea Corrias
Mostrati risultati da 1 a 20 di 40
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