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Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 1983 Cerutti F; David O; Dianzani I; Guidoni C; Ramenghi U; Vigo A; Sacchetti C.
Wolfram's syndrome. Presentation of a case. 1984 Cerutti F; Balboni R; Dianzani I; Guidoni C.
Insulin-dependent diabetes mellitus and maternal age. 1984 Cerutti F; Balboni R; Dianzani I; Guidoni C; Vigo A.
Evaluation of ouabain-insensitive red blood cell cation transport in obese children. 1985 Urbino A; Dianzani I; Boero R; Guarena C; Quarello F; Cerutti F.
Abnormalities of sodium transport by sodium, potassium-activated adenosine triphosphatase in erythrocytes from obese children. 1988 Dianzani I; Boero R; Guarena C; Urbino A; Corda G; Quarello F; Cerutti F.
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 1989 RAMENGHI U; DAVID O; DIANZANI I; SACCHETTI L; BIASI F; CHIARPOTTO E; POLI G
Course of retinopathy in children and adolescents with insulin-dependent diabetes mellitus: a ten-year study. 1989 Cerutti F; Sacchetti C; Vigo A; Dianzani I; Baratono S; Bessone A; Vaona P; Furlotti F.
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype. 1990 Ponzone A; Blau N; Guardamagna O; Ferrero GB; Dianzani I; Endres W.
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy. 1990 Dianzani I; Devoto M; Camaschella C; Saglio G; Ferrero GB; Cerone R; Romano C; Romeo G; Giovannini M; Riva E; et al.
Haplotype distribution and molecular defects of PKU in Italy. 1990 Dianzani I; Camaschella C; Saglio G; Ferrero GB; Romeo G; Devoto M; Romano C; Cerone R; Giovannini M; Riva E; et al.
Erythrocyte sodium-lithium countertransport in diabetic adolescents. 1990 Guarena C; Boero R; Quarello F; Rolando B; Sacchetti C; Dianzani I; Maffei S; Cerutti F; Piccoli G.
Erythrocyte Na,Li countertransport and arterial pressure in diabetic adolescents. 1990 Dianzani I; Boero R; Rolando B; Guarena C; Sacchetti C; Coppo R; Quarello F; Cerutti F.
Tetrahydrobiopterin loading test in hyperphenylalaninemia. 1991 Ponzone A; Guardamagna O; Ferraris S; Ferrero GB; Dianzani I; Cotton RG.
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F 1993 Gasparini, P; Borgato, L; Piperno, A; Girelli, D; Olivieri, O; Gottardi, E; Roetto, A; Dianzani, I; Fargion, S; Schinaia, G
Prenatal diagnosis in primary hyperphenylalaninemias. 1993 Ponzone A; Dianzani I; Spada M; De Sanctis L; Guardamagna O; Viora E; Ponzone R; Kierat L; Leimbacher W; Matasovic A; Blau N
Catalytic activity of tetrahydrobiopterin in dihydropteridine reductase deficiency and indications for treatment. 1993 Ponzone A; Guardamagna O; Dianzani I; Ponzone R; Ferrero GB; Spada M; Cotton RG.
Construction of a genetic map telomeric to HAL-A by microsatellite analysis 1993 Camaschella, C; Roetto, A.; De Sandre, G.; Piperno, A.; Totaro, A.; Dianzani, I.; Gasparini, P.
Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation. 1993 Dianzani I; Camaschella C; Saglio G; Ferrero GB; Ramus S; Ponzone A; Cotton RG.
Genetic history of hyperphenylalaninemias in Italy 1994 Dianzani I; Giannattasio S; De Sanctis L; Alliaudi C; Marra E; Ponzone A; Camaschella C; Piazza A.
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 1994 U. Ramenghi; L. Ruggeri; I. Dianzani; C. Rosso; M.F. Brizzi; C. Camaschella; T. Pietsch; G. Saglio
Mostrati risultati da 1 a 20 di 54
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