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
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
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.
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
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 | |
| 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 | |
| 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. | |
| 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 | |
| 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 |