Sfoglia per Autore
Molecular basis of Phenylketonuria.
1995-01-01 Giannattasio S; Dianzani I; De Sanctis L; Dompè C; Lattanzio P; Alliaudi C; Carnevale F; Ponzone A; Marra E.
Molecular basis of Dihydropterine Reductase Deficiency.
1995-01-01 Dianzani I; Alliaudi C; Dompè C; De Sanctis L; Ponzone A.
Genotype-phenotype correlation in phenylketonuria.
1996-01-01 Dianzani I; Giannattasio S; De Sanctis L; Spada M; Alliaudi C; Lattanzio P; Carnevale F; Marra E; Ponzone A.
Inborn errors of neurotransmitter metabolism: from Phenotype to Genotype
1996-01-01 Carbonara C; Dianzani I; Spada M; Ferrero GB; De Sanctis L; De Luca F; Ponzone A.
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia.
1996-01-01 Dianzani I; Garelli E; Dompè C; Crescenzio N; Locatelli F; Schilirò G; Castaman G; Bagnara GP; Olivieri NF; Gabutti V; Ramenghi U
Phenotyping of phenylketonuric patients by oral phenylalanine loading.
1996-01-01 Ponzone A; Spada M; de Sanctis L; Dianzani I.
Diamond-Blackfan anemia: a congenital defect in erythropoiesis
1996-01-01 DIANZANI I; GARELLI E; U. RAMENGHI
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation
1997-01-01 Dianzani U; Bragardo M; DiFranco D; Alliaudi C; Scagni P; Buonfiglio D; Redoglia V; Bonissoni S; Correra A; Dianzani I; Ramenghi U.
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q.
1997-01-01 DIANZANI I; GARELLI E; CRESCENZIO N; TIMEUS F; MORI PG; VAROTTO S; NOBILI B; BRANDALISE S; OLIVIERI NF; GABUTTI V; U. RAMENGHI
Ipoplasie midollari congenite
1998-01-01 Dianzani I; Ramenghi U
La scelta vita/morte del linfocita.112: 297-309, 1998.
1998-01-01 Dianzani U; Dianzani I; Ramenghi U
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity.
1998-01-01 Gustavsson P; Garelli E; Draptchinskaia N; Ball S; Willig TN; Tentler D; Dianzani I; Punnett HH; Shafer FE; Cario H; Ramenghi U; Glomstein A; Pfeiffer RA; Goringe A; Olivieri NF; Smibert E; Tchernia G; Elinder G; Dahl N
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, Italy
1999-01-01 I. DIANZANI; U. LANDEGREN; C. CAMASCHELLA; A. PONZONE; A. PIAZZA; R.G.H. COTTON
Diamond Blackfan anaemia in the Italian population
1999-01-01 U. RAMENGHI; GARELLI E.; VALTOLINA S.; CAMPAGNOLI MF.; TIMEUS F.; CRESCENZIO N; MAIR M.; VAROTTO S.; D'AVANZO S.; NOBILI B.; MASSOLO F.; MORI PG.; LOCATELLI F.; GUSTAVSSON P.; DAHL N.; DIANZANI I.
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression
1999-01-01 WILLIG TH; DRAPTCHINSKAIA N; DIANZANI I; BALL S; NIEMEYER C; RAMENGHI U; ORFALI K; GUSTAVSSON P; GARELLI E; A. BRUSCO; TIEMANN C; PERIGNON JL; BOUCHIER C; CICCHIELLO L; DAHL N; MOHANDAS N; TCHERNIA G
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children.
2000-01-01 PIGNATA C; ALESSIO M; RAMENGHI U; BONISSONI S; DIFRANCO D; BRUSCO A; MATRECANO E; FRANZESE A; DIANZANI I; DIANZANI U
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer.
2000-01-01 U. RAMENGHI; BONISSONI S; MIGLIARETTI G; DEFRANCO S; GAMBARUTO C; DIFRANCO D; PRIORI R; CONTI F; DIANZANI I; VALESINI G; MERLETTI F; DIANZANI U
Diamond-Blackfan Anemia: an Overview
2000-01-01 DIANZANI I; GARELLI E; U. RAMENGHI
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases.
2003-01-01 BONA G; DEFRANCO S; CHIOCCHETTI A; INDELICATO M; BIAVA A; DIFRANCO D; DIANZANI I; U. RAMENGHI; CORRIAS A; WEBER G; DE SANCTIS V; IUGHETTI L; RADETTI G; DIANZANI U.
Basi molecolari delle aplasie ereditarie
2004-01-01 A. SAVOIA; U. RAMENGHI; I. DIANZANI
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Molecular basis of Phenylketonuria. | 1995 | Giannattasio S; Dianzani I; De Sanctis L; Dompè C; Lattanzio P; Alliaudi C; Carnevale F; Ponzone A; Marra E. | |
| Molecular basis of Dihydropterine Reductase Deficiency. | 1995 | Dianzani I; Alliaudi C; Dompè C; De Sanctis L; Ponzone A. | |
| Genotype-phenotype correlation in phenylketonuria. | 1996 | Dianzani I; Giannattasio S; De Sanctis L; Spada M; Alliaudi C; Lattanzio P; Carnevale F; Marra E; Ponzone A. | |
| Inborn errors of neurotransmitter metabolism: from Phenotype to Genotype | 1996 | Carbonara C; Dianzani I; Spada M; Ferrero GB; De Sanctis L; De Luca F; Ponzone A. | |
| Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. | 1996 | Dianzani I; Garelli E; Dompè C; Crescenzio N; Locatelli F; Schilirò G; Castaman G; Bagnara GP; Olivieri NF; Gabutti V; Ramenghi U | |
| Phenotyping of phenylketonuric patients by oral phenylalanine loading. | 1996 | Ponzone A; Spada M; de Sanctis L; Dianzani I. | |
| Diamond-Blackfan anemia: a congenital defect in erythropoiesis | 1996 | DIANZANI I; GARELLI E; U. RAMENGHI | |
| Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation | 1997 | Dianzani U; Bragardo M; DiFranco D; Alliaudi C; Scagni P; Buonfiglio D; Redoglia V; Bonissoni S; Correra A; Dianzani I; Ramenghi U. | |
| Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q. | 1997 | DIANZANI I; GARELLI E; CRESCENZIO N; TIMEUS F; MORI PG; VAROTTO S; NOBILI B; BRANDALISE S; OLIVIERI NF; GABUTTI V; U. RAMENGHI | |
| Ipoplasie midollari congenite | 1998 | Dianzani I; Ramenghi U | |
| La scelta vita/morte del linfocita.112: 297-309, 1998. | 1998 | Dianzani U; Dianzani I; Ramenghi U | |
| Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity. | 1998 | Gustavsson P; Garelli E; Draptchinskaia N; Ball S; Willig TN; Tentler D; Dianzani I; Punnett HH; Shafer FE; Cario H; Ramenghi U; Glomstein A; Pfeiffer RA; Goringe A; Olivieri NF; Smibert E; Tchernia G; Elinder G; Dahl N | |
| Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, Italy | 1999 | I. DIANZANI; U. LANDEGREN; C. CAMASCHELLA; A. PONZONE; A. PIAZZA; R.G.H. COTTON | |
| Diamond Blackfan anaemia in the Italian population | 1999 | U. RAMENGHI; GARELLI E.; VALTOLINA S.; CAMPAGNOLI MF.; TIMEUS F.; CRESCENZIO N; MAIR M.; VAROTTO S.; D'AVANZO S.; NOBILI B.; MASSOLO F.; MORI PG.; LOCATELLI F.; GUSTAVSSON P.; DAHL N.; DIANZANI I. | |
| Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression | 1999 | WILLIG TH; DRAPTCHINSKAIA N; DIANZANI I; BALL S; NIEMEYER C; RAMENGHI U; ORFALI K; GUSTAVSSON P; GARELLI E; A. BRUSCO; TIEMANN C; PERIGNON JL; BOUCHIER C; CICCHIELLO L; DAHL N; MOHANDAS N; TCHERNIA G | |
| Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. | 2000 | PIGNATA C; ALESSIO M; RAMENGHI U; BONISSONI S; DIFRANCO D; BRUSCO A; MATRECANO E; FRANZESE A; DIANZANI I; DIANZANI U | |
| Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. | 2000 | U. RAMENGHI; BONISSONI S; MIGLIARETTI G; DEFRANCO S; GAMBARUTO C; DIFRANCO D; PRIORI R; CONTI F; DIANZANI I; VALESINI G; MERLETTI F; DIANZANI U | |
| Diamond-Blackfan Anemia: an Overview | 2000 | DIANZANI I; GARELLI E; U. RAMENGHI | |
| Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. | 2003 | BONA G; DEFRANCO S; CHIOCCHETTI A; INDELICATO M; BIAVA A; DIFRANCO D; DIANZANI I; U. RAMENGHI; CORRIAS A; WEBER G; DE SANCTIS V; IUGHETTI L; RADETTI G; DIANZANI U. | |
| Basi molecolari delle aplasie ereditarie | 2004 | A. SAVOIA; U. RAMENGHI; I. DIANZANI |
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