Sfoglia per Autore
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family
2006-01-01 CAMPAGNOLI MF; PUCCI A; GARELLI E; CARANDO A; DEFILIPPI C; LALA R; INGROSSO G; DIANZANI I; FORNI M; RAMENGHI U
The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients
2006-01-01 CAMPAGNOLI MF; GARBARINI L; QUARELLO P; GARELLI E; CARANDO A; BARAVALLE V; DORIA A; BIAVA A; CHIOCCHETTI A; ROSOLEN A; DUFOUR C; DIANZANI U; RAMENGHI U
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein
2005-01-01 CHIOCCHETTI A; GIBELLO L; CARANDO A; ASPESI A; SECCO P; GARELLI E; LORENI F; ANGELINI M; BIAVA A; DAHL N; DIANZANI U; RAMENGHI U; SANTORO C; DIANZANI I
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia
2005-01-01 GARELLI E; QUARELLO P; CAMPAGNOLI MF; BRUSCO A; CARANDO A; MENEGATTI E; CRESCENZIO N; FOGLIA L; DIANZANI I; RAMENGHI U
Search for protein interactors of ribosomal protein S19, mutated in Diamond Blackfan Anemia
2005-01-01 I. DIANZANI; A. CHIOCCHETTI; L. GIBELLO; A. CARANDO; P. SECCO; A. BIAVA; A. ASPESI; U. DIANZANI; U. RAMENGHI; S. ORR; M. ANGELINI; M. CATERINO; M. RUOPPOLO; F. LORENI; C. SANTORO
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature
2004-01-01 CAMPAGNOLI MF; GARELLI E; QUARELLO P; CARANDO A; VAROTTO S; NOBILI B; LONGONI D; PECILE V; ZECCA M; DUFOUR C; RAMENGHI U; DIANZANI I
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica.
2004-01-01 QUARELLO P; CAMPAGNOLI MF; GARELLI E; CARANDO A; CRESCENZIO N; DORIA A; MARTINO S; RENGA D; U. RAMENGHI; DIANZANI I
Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene.
2003-01-01 Dianzani I; Garelli E; Gustavsson P; Carando A; Gustafsson B; Dahl N; Annerén G.
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population.
2000-01-01 U. RAMENGHI; CAMPAGNOLI MF; GARELLI E; CARANDO A; BRUSCO A; BAGNARA GP; STRIPPOLI PL; IZZI GC; BRANDALISE S; RICCARDI R; DIANZANI I
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family | 2006 | CAMPAGNOLI MF; PUCCI A; GARELLI E; CARANDO A; DEFILIPPI C; LALA R; INGROSSO G; DIANZANI I; FORNI M; RAMENGHI U | |
| The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients | 2006 | CAMPAGNOLI MF; GARBARINI L; QUARELLO P; GARELLI E; CARANDO A; BARAVALLE V; DORIA A; BIAVA A; CHIOCCHETTI A; ROSOLEN A; DUFOUR C; DIANZANI U; RAMENGHI U | |
| Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein | 2005 | CHIOCCHETTI A; GIBELLO L; CARANDO A; ASPESI A; SECCO P; GARELLI E; LORENI F; ANGELINI M; BIAVA A; DAHL N; DIANZANI U; RAMENGHI U; SANTORO C; DIANZANI I | |
| Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia | 2005 | GARELLI E; QUARELLO P; CAMPAGNOLI MF; BRUSCO A; CARANDO A; MENEGATTI E; CRESCENZIO N; FOGLIA L; DIANZANI I; RAMENGHI U | |
| Search for protein interactors of ribosomal protein S19, mutated in Diamond Blackfan Anemia | 2005 | I. DIANZANI; A. CHIOCCHETTI; L. GIBELLO; A. CARANDO; P. SECCO; A. BIAVA; A. ASPESI; U. DIANZANI; U. RAMENGHI; S. ORR; M. ANGELINI; M. CATERINO; M. RUOPPOLO; F. LORENI; C. SANTORO | |
| Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature | 2004 | CAMPAGNOLI MF; GARELLI E; QUARELLO P; CARANDO A; VAROTTO S; NOBILI B; LONGONI D; PECILE V; ZECCA M; DUFOUR C; RAMENGHI U; DIANZANI I | |
| Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. | 2004 | QUARELLO P; CAMPAGNOLI MF; GARELLI E; CARANDO A; CRESCENZIO N; DORIA A; MARTINO S; RENGA D; U. RAMENGHI; DIANZANI I | |
| Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene. | 2003 | Dianzani I; Garelli E; Gustavsson P; Carando A; Gustafsson B; Dahl N; Annerén G. | |
| Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. | 2000 | U. RAMENGHI; CAMPAGNOLI MF; GARELLI E; CARANDO A; BRUSCO A; BAGNARA GP; STRIPPOLI PL; IZZI GC; BRANDALISE S; RICCARDI R; DIANZANI I |
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