Objective: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease characterized by recurrent fractures, blue sclera, and hearing loss. Bisphosphonate treatment has been reported to decrease the annual number of fractures and improve the quality of life in patients with OI. The aim of this study is to evaluate the effect of bisphosphonate treatment in the Turkish OI cohort
UNLABELLED: Bisphosphonates can increase bone mineral density (BMD) in children with osteogenesis im...
PurposeThis study aimed to investigate the skeletal outcomes of patients with osteogenesis imperfect...
Aims: Osteogenesis imperfecta (OI) is a rare inherited disorder causing low bone density and increas...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
WOS: 000238794300006PubMed ID: 16848111Different therapy models have been tried in order to decrease...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Background/Aims: Intravenous bisphosphonate therapy is the first-line treatment in moderate-to-sever...
Osteogenesis imperfecta is a heterogeneous group of inherited disorders chiefly affecting type I col...
Abstract Osteogenesis imperfecta (OI) is characterized by low bone mass and bone fragility. Using da...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
Background. Osteogenesis imperfecta is a heritable disorder of bone connective tissue. Type III has ...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
Osteogenezis imperfekta düşük kemik kitlesi ve artmış kemik frajilitesi ile karakterize ektraselüler...
BackgroundInformation on the long-term efficacy of intravenous pamidronate therapy in Asian patients...
Aim: To find an effective symptomatic treatment for osteogenesis imperfecta (OI). Methods: In a pros...
UNLABELLED: Bisphosphonates can increase bone mineral density (BMD) in children with osteogenesis im...
PurposeThis study aimed to investigate the skeletal outcomes of patients with osteogenesis imperfect...
Aims: Osteogenesis imperfecta (OI) is a rare inherited disorder causing low bone density and increas...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
WOS: 000238794300006PubMed ID: 16848111Different therapy models have been tried in order to decrease...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Background/Aims: Intravenous bisphosphonate therapy is the first-line treatment in moderate-to-sever...
Osteogenesis imperfecta is a heterogeneous group of inherited disorders chiefly affecting type I col...
Abstract Osteogenesis imperfecta (OI) is characterized by low bone mass and bone fragility. Using da...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
Background. Osteogenesis imperfecta is a heritable disorder of bone connective tissue. Type III has ...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
Osteogenezis imperfekta düşük kemik kitlesi ve artmış kemik frajilitesi ile karakterize ektraselüler...
BackgroundInformation on the long-term efficacy of intravenous pamidronate therapy in Asian patients...
Aim: To find an effective symptomatic treatment for osteogenesis imperfecta (OI). Methods: In a pros...
UNLABELLED: Bisphosphonates can increase bone mineral density (BMD) in children with osteogenesis im...
PurposeThis study aimed to investigate the skeletal outcomes of patients with osteogenesis imperfect...
Aims: Osteogenesis imperfecta (OI) is a rare inherited disorder causing low bone density and increas...