CASTELLANI, ALESSANDRO
CASTELLANI, ALESSANDRO
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta.
1987-01-01 Dyne, KATHARINE MARY; Cetta, Giuseppe; Tenni, Ruggero; Rossi, Antonio; Finardi, E; Brunelli, Pc; Castellani, Alessandro
MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN
1989-01-01 Galliano, Monica; Minchiotti, Lorenzo; Iadarola, Paolo; Stoppini, Monica; Porta, F; Castellani, Alessandro
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects.
1987-01-01 Leoni, A; Cetta, Giuseppe; Tenni, Ruggero; Pasquali Ronchetti, I; Bertolini, F; Guerra, D; Dyne, KATHARINE MARY; Castellani, Alessandro
Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts.
1984-01-01 De Luca, Giancarlo; Tira, MARIA ENRICA; Rindi, Simonetta; Salvini, Roberta; Cetta, Giuseppe; Castellani, Alessandro
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity.
1988-01-01 Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Valli, Maurizia; Zanaboni, Giuseppe; Castellani, Alessandro
The role of UDP-sugars synthesizing enzymes in the regulation of glycosaminoglycan biosynthesis.
1988-01-01 DE LUCA, Giancarlo; Rindi, Simonetta; Salvini, Roberta; Tira, MARIA ENRICA; Castellani, Alessandro
Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. Defective pro-alpha 1(I) chains in a patient with abnormal proteoglycan metabolism and mineral deposits in the dermis.
1988-01-01 Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Rossi, Antonio; Quacci, D; Lenzi, L; Castellani, Alessandro
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. | 1-gen-1987 | Dyne, KATHARINE MARY; Cetta, Giuseppe; Tenni, Ruggero; Rossi, Antonio; Finardi, E; Brunelli, Pc; Castellani, Alessandro | |
| MOLECULAR DEFECTS IN GENETIC VARIANTS OF HUMAN SERUM ALBUMIN | 1-gen-1989 | Galliano, Monica; Minchiotti, Lorenzo; Iadarola, Paolo; Stoppini, Monica; Porta, F; Castellani, Alessandro | |
| Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. | 1-gen-1987 | Leoni, A; Cetta, Giuseppe; Tenni, Ruggero; Pasquali Ronchetti, I; Bertolini, F; Guerra, D; Dyne, KATHARINE MARY; Castellani, Alessandro | |
| Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts. | 1-gen-1984 | De Luca, Giancarlo; Tira, MARIA ENRICA; Rindi, Simonetta; Salvini, Roberta; Cetta, Giuseppe; Castellani, Alessandro | |
| Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. | 1-gen-1988 | Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Valli, Maurizia; Zanaboni, Giuseppe; Castellani, Alessandro | |
| The role of UDP-sugars synthesizing enzymes in the regulation of glycosaminoglycan biosynthesis. | 1-gen-1988 | DE LUCA, Giancarlo; Rindi, Simonetta; Salvini, Roberta; Tira, MARIA ENRICA; Castellani, Alessandro | |
| Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. Defective pro-alpha 1(I) chains in a patient with abnormal proteoglycan metabolism and mineral deposits in the dermis. | 1-gen-1988 | Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Rossi, Antonio; Quacci, D; Lenzi, L; Castellani, Alessandro |