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pro vyhledávání: '"Saverio Liuzza"'
Autor:
Luca Idolazzi, Ombretta Viapiana, Davide Gatti, Maria Rosaria Povino, Elena Fracassi, Maurizio Rossini, Saverio Liuzza, Silvano Adami
Publikováno v:
Calcified Tissue International. 93:448-452
Osteogenesis imperfecta (OI) is a hereditary disease characterized by low bone mass, increased bone fragility, short stature, and skeletal deformities. This study focuses on OI type I, the mildest form of the disease. Bisphosphonates represent the pr