BackgroundPatients with severe osteogenesis imperfecta (OI; MIM number 259420) suffer from low bone mass, fractures, and bone pain since birth, and have poor prognosis. This study assessed the outcome of patients with severe OI who were treated with cyclic pamidronate prior to the age of 1 year.MethodsThe six patients, who had bone fractures either in utero or in their 1st month of life, were treated with cyclic pamidronate from a mean age of 2.8 months.ResultsAll the patients tolerated the infusion, except for having transient hypocalcemia at the first infusion. Decreases in irritability and improvements in feeding were observed 2–3 months after the first infusion. All patients showed a rapid increase in bone mineral density over the first...
Objective To evaluate prospectively the efficacy of bisphosphonate treatment in infants with severe ...
Abstract Intravenous treatment with pamidronate is beneficial in children and adolescents with moder...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
Background: Patients with severe osteogenesis imperfecta (01; MIM number 259420) suffer from low bon...
BackgroundPatients with severe osteogenesis imperfecta (OI; MIM number 259420) suffer from low bone ...
BackgroundInformation on the long-term efficacy of intravenous pamidronate therapy in Asian patients...
Severe osteogenesis imperfecta (OI) is a hereditary disorder char-acterized by increased bone fragil...
OBJECTIVE: Evaluate clinical outcome of early cyclic intravenous pamidronate treatment in children w...
Objective: Evaluate clinical outcome of early cyclic intravenous pamidronate treatment in children w...
Cyclical neridronate treatment, started just after diagnosis at birth, had positive effects on growt...
Purpose Osteoporosis is a skeletal disorder characterized by reduced bone mass that results in incre...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Intravenous neridronate infusions, administered quarterly, significantly increase BMD and lower the ...
Abstract Osteogenesis imperfecta is a hereditary disorder of connective tissues characterised by low...
Objective To evaluate prospectively the efficacy of bisphosphonate treatment in infants with severe ...
Abstract Intravenous treatment with pamidronate is beneficial in children and adolescents with moder...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
Background: Patients with severe osteogenesis imperfecta (01; MIM number 259420) suffer from low bon...
BackgroundPatients with severe osteogenesis imperfecta (OI; MIM number 259420) suffer from low bone ...
BackgroundInformation on the long-term efficacy of intravenous pamidronate therapy in Asian patients...
Severe osteogenesis imperfecta (OI) is a hereditary disorder char-acterized by increased bone fragil...
OBJECTIVE: Evaluate clinical outcome of early cyclic intravenous pamidronate treatment in children w...
Objective: Evaluate clinical outcome of early cyclic intravenous pamidronate treatment in children w...
Cyclical neridronate treatment, started just after diagnosis at birth, had positive effects on growt...
Purpose Osteoporosis is a skeletal disorder characterized by reduced bone mass that results in incre...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic pamidron...
Intravenous neridronate infusions, administered quarterly, significantly increase BMD and lower the ...
Abstract Osteogenesis imperfecta is a hereditary disorder of connective tissues characterised by low...
Objective To evaluate prospectively the efficacy of bisphosphonate treatment in infants with severe ...
Abstract Intravenous treatment with pamidronate is beneficial in children and adolescents with moder...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...