Background/Aims: Intravenous bisphosphonate therapy is the first-line treatment in moderate-to-severe osteogenesis imperfecta (OI), but there are varied treatment protocols with little data on long-term efficacy. This study evaluates the clinical outcomes when transitioning from active bisphosphonate treatment to maintenance therapy. Methods: A retrospective review was conducted on 17 patients before treatment, following active treatment (zoledronate 0.05 mg/kg 6-monthly or pamidronate 6-9 mg/kg/year) and after establishment on maintenance treatment for more than 2 years (zoledronate 0.025 mg/kg 6-monthly or pamidronate <4 mg/kg/year). Results: There was a significant reduction in mean fracture rate from 1.5 +/- 1.1 fractures/year at baseli...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Objective: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease charac...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
WOS: 000238794300006PubMed ID: 16848111Different therapy models have been tried in order to decrease...
Aim: To find an effective symptomatic treatment for osteogenesis imperfecta (OI). Methods: In a pros...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
Objective To evaluate prospectively the efficacy of bisphosphonate treatment in infants with severe ...
Pamidronate (PAM) infusion is the standard treatment in children with osteogenesis imperfecta (OI). ...
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...
Introduction: Osteogenesis imperfecta (OI) is a group of genetic disorders with collagen bone defec...
Low bone density for age is becoming an increasingly recognized problem in the pediatric world. It c...
While bisphosphonates reduce fracture risk over 3 to 5 years, the optimal duration of treatment is u...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Objective: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease charac...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
WOS: 000238794300006PubMed ID: 16848111Different therapy models have been tried in order to decrease...
Aim: To find an effective symptomatic treatment for osteogenesis imperfecta (OI). Methods: In a pros...
Background: Osteogenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of seve...
Osteogenesis imperfecta is a genetic disorder of extracellular matrix, characterized with decreased ...
Objective To evaluate prospectively the efficacy of bisphosphonate treatment in infants with severe ...
Pamidronate (PAM) infusion is the standard treatment in children with osteogenesis imperfecta (OI). ...
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...
Introduction: Osteogenesis imperfecta (OI) is a group of genetic disorders with collagen bone defec...
Low bone density for age is becoming an increasingly recognized problem in the pediatric world. It c...
While bisphosphonates reduce fracture risk over 3 to 5 years, the optimal duration of treatment is u...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Background/Aims: To systematically assess contemporary knowledge regarding the effectiveness and saf...
Objective: Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease charac...