SAVOLDI, Gianfranco
SAVOLDI, Gianfranco
Dipartimento di Scienze Cliniche e Sperimentali
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms.
2007-01-01 Donini, M; Fontana, Stefania; Savoldi, Gianfranco; Vermi, William; Tassone, Laura; Gentili, Francesca; Zenaro, E; Ferrari, Daniela; Notarangelo, Luigi Daniele; Porta, Fulvio; Facchetti, Fabio; Dusi, S; Badolato, Raffaele
Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing Genotype
2022-01-01 Izzi, C.; Dordoni, C.; Delbarba, E.; Mazza, C.; Savoldi, G.; Econimo, L.; Cortinovis, R.; Zeni, L.; Martin, E.; Alberici, F.; Scolari, F.
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review
2019-01-01 Dordoni, C.; Prefumo, F.; Iascone, M.; Pinelli, L.; Palumbo, G.; Bondioni, M. P.; Savoldi, G.; Donzelli, C.; Sartori, E.; Valente, E. M.; Izzi, C.
PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients
2010-01-01 Chiarini, M.; Sabelli, C.; Melotti, P.; Garlanda, C.; Savoldi, G.; Mazza, C.; Padoan, R.; Plebani, A.; Mantovani, A.; Notarangelo, L. D.; Assael, B. M.; Badolato, R.
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations
2014-01-01 Notarangelo, Lucia Dora; Savoldi, Gianfranco; Cavagnini, Sara; Bennato, Veronica; Vasile, Sabrina; Pilotta, Alba; Plebani, Alessandro; Porta, Fulvio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. | 1-gen-2007 | Donini, M; Fontana, Stefania; Savoldi, Gianfranco; Vermi, William; Tassone, Laura; Gentili, Francesca; Zenaro, E; Ferrari, Daniela; Notarangelo, Luigi Daniele; Porta, Fulvio; Facchetti, Fabio; Dusi, S; Badolato, Raffaele | |
| Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing Genotype | 1-gen-2022 | Izzi, C.; Dordoni, C.; Delbarba, E.; Mazza, C.; Savoldi, G.; Econimo, L.; Cortinovis, R.; Zeni, L.; Martin, E.; Alberici, F.; Scolari, F. | |
| Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review | 1-gen-2019 | Dordoni, C.; Prefumo, F.; Iascone, M.; Pinelli, L.; Palumbo, G.; Bondioni, M. P.; Savoldi, G.; Donzelli, C.; Sartori, E.; Valente, E. M.; Izzi, C. | |
| PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients | 1-gen-2010 | Chiarini, M.; Sabelli, C.; Melotti, P.; Garlanda, C.; Savoldi, G.; Mazza, C.; Padoan, R.; Plebani, A.; Mantovani, A.; Notarangelo, L. D.; Assael, B. M.; Badolato, R. | |
| Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations | 1-gen-2014 | Notarangelo, Lucia Dora; Savoldi, Gianfranco; Cavagnini, Sara; Bennato, Veronica; Vasile, Sabrina; Pilotta, Alba; Plebani, Alessandro; Porta, Fulvio |