VENTURI, Giacomo
VENTURI, Giacomo
DIPARTIMENTO DI SCIENZE DELLA VITA E DELLA RIPRODUZIONE (attivo dal 01/01/2000 al 31/12/2015)
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect
2012-01-01 Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, Alberto; Valenti, Maria Teresa; Boner, Attilio; Antoniazzi, Franco
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI
2011-01-01 Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, A.; Valenti, Maria Teresa; Morandi, Grazia; Doro, F.; Maines, E.; Boner, Attilio; Antoniazzi, Franco
Current and emerging treatments for the management of osteogenesis imperfecta
2010-01-01 Monti, Elena; Mottes, Monica; Fraschini, P.; Brunelli, P. C.; Forlino, A.; Venturi, Giacomo; Doro, F.; Perlini, S.; Cavarzere, P.; Antoniazzi, Franco
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I
2011-01-01 Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M; Pelilli, E; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco
GH in combination with bisphosphonate treatment in osteogenesis imperfecta
2010-01-01 Antoniazzi, Franco; Monti, Elena; Venturi, Giacomo; Franceschi, R.; Doro, F.; Gatti, Davide; Zamboni, Giorgio; Tatò, L.
Growth Hormone in Combination with Bisphosphonate Treatment in Osteogenesis Imperfecta.
2010-01-01 Doro, Francesco; Cavarzere, Paolo; Monti, Elena; Venturi, Giacomo; Adami, Silvano; Antoniazzi, Franco
How to cope with a severe skeletal dysplasia
2010-01-01 Monti, Elena; Grazzina, Nicoletta; Corradi, Massimiliano; Gandini, Alberto; Venturi, Giacomo; Doro, Francesco; Morandi, G.; Maines, Evelina; Pietrobelli, Angelo; Antoniazzi, Franco; Padovani, Ezio Maria
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta
2011-01-01 Doro, F.; Monti, Elena; Morandi, Grazia; Maines, E.; Brugnara, Milena; Gandini, A.; Corradi, Massimiliano; Venturi, Giacomo; Antoniazzi, Franco
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism
2014-01-01 Vincenzi, Monica; Camilot, Marta; Ferrarini, Eleonora; Teofoli, Francesca; Venturi, Giacomo; Gaudino, Rossella; Cavarzere, Paolo; De Marco, Giuseppina; Agretti, Patrizia; Dimida, Antonio; Tonacchera, Massimo; Boner, Attilio; Antoniazzi, Franco
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen
2012-01-01 Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M.; Pelilli, E.; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco
Molecular screening in OI patients at Verona reference center: typical mutations
2005-01-01 Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Lievore, C.; Antoniazzi, Franco; Tato', Luciano
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta.
2011-01-01 Maines, Evelina; Monti, Elena; Doro, Francesco; Morandi, G; Venturi, Giacomo; Corradi, Massimiliano; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta
2011-01-01 Corradi, Massimiliano; Venturi, Giacomo; Monti, Elena; Gandini, Alberto; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa; Morandi, G; Doro, Francesco; Maines, Evelina; Boner, Attilio; Antoniazzi, Franco
Osteogenesis imperfecta and its molecular diagnosis by determination of mutations of type I collagen genes
2006-01-01 Tedeschi, Elisa; Antoniazzi, Franco; Venturi, Giacomo; Zamboni, Giorgio; Tato', Luciano
Osteogenesis Imperfecta: clinical, biochemical and molecular findings
2006-01-01 Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Valli, M.; Camilot, Marta; Viglio, S.; Antoniazzi, Franco; Tato', Luciano
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene
2014-01-01 Corradi, Massimiliano; Monti, E.; Venturi, Giacomo; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect | 1-gen-2012 | Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, Alberto; Valenti, Maria Teresa; Boner, Attilio; Antoniazzi, Franco | |
| A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI | 1-gen-2011 | Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, A.; Valenti, Maria Teresa; Morandi, Grazia; Doro, F.; Maines, E.; Boner, Attilio; Antoniazzi, Franco | |
| Current and emerging treatments for the management of osteogenesis imperfecta | 1-gen-2010 | Monti, Elena; Mottes, Monica; Fraschini, P.; Brunelli, P. C.; Forlino, A.; Venturi, Giacomo; Doro, F.; Perlini, S.; Cavarzere, P.; Antoniazzi, Franco | |
| Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I | 1-gen-2011 | Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M; Pelilli, E; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco | |
| GH in combination with bisphosphonate treatment in osteogenesis imperfecta | 1-gen-2010 | Antoniazzi, Franco; Monti, Elena; Venturi, Giacomo; Franceschi, R.; Doro, F.; Gatti, Davide; Zamboni, Giorgio; Tatò, L. | |
| Growth Hormone in Combination with Bisphosphonate Treatment in Osteogenesis Imperfecta. | 1-gen-2010 | Doro, Francesco; Cavarzere, Paolo; Monti, Elena; Venturi, Giacomo; Adami, Silvano; Antoniazzi, Franco | |
| How to cope with a severe skeletal dysplasia | 1-gen-2010 | Monti, Elena; Grazzina, Nicoletta; Corradi, Massimiliano; Gandini, Alberto; Venturi, Giacomo; Doro, Francesco; Morandi, G.; Maines, Evelina; Pietrobelli, Angelo; Antoniazzi, Franco; Padovani, Ezio Maria | |
| Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta | 1-gen-2011 | Doro, F.; Monti, Elena; Morandi, Grazia; Maines, E.; Brugnara, Milena; Gandini, A.; Corradi, Massimiliano; Venturi, Giacomo; Antoniazzi, Franco | |
| Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism | 1-gen-2014 | Vincenzi, Monica; Camilot, Marta; Ferrarini, Eleonora; Teofoli, Francesca; Venturi, Giacomo; Gaudino, Rossella; Cavarzere, Paolo; De Marco, Giuseppina; Agretti, Patrizia; Dimida, Antonio; Tonacchera, Massimo; Boner, Attilio; Antoniazzi, Franco | |
| Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen | 1-gen-2012 | Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M.; Pelilli, E.; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco | |
| Molecular screening in OI patients at Verona reference center: typical mutations | 1-gen-2005 | Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Lievore, C.; Antoniazzi, Franco; Tato', Luciano | |
| No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. | 1-gen-2011 | Maines, Evelina; Monti, Elena; Doro, Francesco; Morandi, G; Venturi, Giacomo; Corradi, Massimiliano; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco | |
| Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta | 1-gen-2011 | Corradi, Massimiliano; Venturi, Giacomo; Monti, Elena; Gandini, Alberto; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa; Morandi, G; Doro, Francesco; Maines, Evelina; Boner, Attilio; Antoniazzi, Franco | |
| Osteogenesis imperfecta and its molecular diagnosis by determination of mutations of type I collagen genes | 1-gen-2006 | Tedeschi, Elisa; Antoniazzi, Franco; Venturi, Giacomo; Zamboni, Giorgio; Tato', Luciano | |
| Osteogenesis Imperfecta: clinical, biochemical and molecular findings | 1-gen-2006 | Venturi, Giacomo; Tedeschi, Elisa; Mottes, Monica; Valli, M.; Camilot, Marta; Viglio, S.; Antoniazzi, Franco; Tato', Luciano | |
| The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene | 1-gen-2014 | Corradi, Massimiliano; Monti, E.; Venturi, Giacomo; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco |