IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 216
Titolo Data di pubblicazione Autore(i) File
ITALIAN STUDY ON THE PTERIDINES METABOLISM IN CHILDREN AFFECTED BY HYPERPHENYLALANINEMIA AND PHENYLKETONURIA 1-gen-1988 Valsasina, R; Riva, E; Biasucci, G; Longhi, R; Giovannini, M
TETRAHYDROBIOPTERIN DEFICIENCY SCREENING IN HYPERPHENYLALANINEMIC CHILDREN 1-gen-1989 Giovannini, M; Valsasina, R; Biasucci, G; Longhi, R; Riva, E
URINARY NEOPTERIN DETERMINATION IN HIV-POSITIVE CHILDREN 1-gen-1989 Valsasina, R; Zuccotti, Gv; Biasucci, G; Pogliani, L; Brioschi, M; Riva, E
Prenatal Diagnosis of Atypical Phenylketonuria 1-gen-1989 N, Blau; A, Niederwieser; H Ch, Curtius; L, Kierat; W, Leimbacher; A, Matasovic; F, Binkert; H, Lehmann; D, Leupold; O, Guardamagna; A, Ponzone; H, Schmidt; T, Coskun; I, Ozalp; R, Giugliani; Biasucci, G; M, Giovannini
etrahydrobiopterin deficiency screening in hyperphenylalaninemic children 1-gen-1989 Giovannini, M; Valsasina, R; Biasucci, G; Longhi, R; Riva, E
Study on the Pteridines Metabolism in Children Affected by Hyperphenylalaninaemia and Phenylketonuria 1-gen-1989 R, Valsasina; E, Riva; Biasucci, G; R, Longhi; M, Giovannini
NEURORADIOLOGICAL IMPROVEMENT AFTER ONE YEAR OF THERAPY IN A CASE OF DHPR DEFICIENCY 1-gen-1990 Biasucci, G; Valsasina, R; Giovannini, M; Brioschi, M; Saleri, L; Riva, E
URINARY-EXCRETION OF PTERINS IN HYPERPHENYLALANINEMIC AND PHENYLKETONURIC PATIENTS 1-gen-1990 Valsasina, R; Riva, E; Longhi, R; Biasucci, G; Giovannini, M
URINARY NEOPTERIN EXCRETION IN A GROUP OF HIV-POSITIVE CHILDREN 1-gen-1990 Zuccotti, Gv; Biasucci, G; Fiocchi, A; Brioschi, M; Pogliani, L; Cerbelli, A; Giovannini, M
Urinary neopterin excretion in a group of HIV-positive children [ESCREZIONE URINARIA DI NEOPTERINA IN UN GRUPPO DI BAMBINI HIV-POSITIVI] 1-gen-1990 Zuccotti, Gv; Biasucci, G; Fiocchi, A; Brioschi, M; Pogliani, L; Cerbelli, A; Giovannini, M
Cofactor defects and PKU: Diagnosis and treatment 1-gen-1991 Giovannini, M; Biasucci, G; Brioschi, ; M, ; Ghiglioni, D; Riva, E
The phenylketonuria: State of the art [LA FENILCHETONURIA OGGI] 1-gen-1992 Giovannini, M; Riva, E; Biasucci, G; Ghiglioni, D
Fatty acids in prevention and therapy in pediatrics 1-gen-1992 Agostoni, C; Riva, E; Biasucci, G
Combined Zidovudine and Interferon-α 2a Therapy in Children with Acquired Immune Deficiency Syndrome 1-gen-1992 M, Giovannini; G, V Zuccotti; Biasucci, G; V, Locatelli; E, Riva
Tyrosinaemia type Ia without excess of urinary succinylacetone 1-gen-1993 Biasucci, G; B, Giuffré; S La, Grutta; E, Riva
Mutational spectrum of phenylalanine hydroxylase deficiency in sicily: Implications for diagnosis of hyperphenyl-alaninemia in Southern Europe 1-gen-1993 Guldberg, P.; Romano, V.; Ceratto, N.; Bosco, P.; Cluna, M.; Indellcato, A.; Mollica, F.; Mell, C.; Glovannini, M.; Riva, E.; Biasucci, G.; Henriksen, K. F.; Guttler, F.
Nutritional aspects of phenylketonuria: Correlation between blood lipids and immunoglobulins G, A and M in a phenylketonuric pediatric population on diet therapy 1-gen-1993 Giovannini, M; Agostoni, C; Bellu, R; Ghiglioni, D; Giuffre, B; Biasucci, G; Riva, E
Tyrosinaemia type Ia without excess of urinary succinylacetone 1-gen-1993 Biasucci, G; B, Giuffrè; S La, Grutta; E, Riva
Nutritional follow-up in treated hyperphenylalaninemias 1-gen-1993 Riva, E; Agostoni, C; Biasucci, G; Cesa-Bianchi, A; Rottoli, A; Giovannini, M
Fatty acid status in treated galactosaemia 1-gen-1994 C, Agostoni; E, Riva; Biasucci, G; D, Luotti; A, Rottoli; M, Giovannini
Mostrati risultati da 1 a 20 di 216
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile