Pamidronate does not adversely affect bone intrinsic material properties in children with osteogenesis imperfecta

M Weber, P Roschger, N Fratzl-Zelman, T Schöberl… - Bone, 2006 - Elsevier
Cyclical intravenous pamidronate therapy increases bone mass in children with
osteogenesis imperfecta (OI), but the effect on the intrinsic material properties of bone is …

Osteogenesis imperfecta type VI in childhood and adolescence: effects of cyclical intravenous pamidronate treatment

C Land, F Rauch, R Travers, FH Glorieux - Bone, 2007 - Elsevier
Cyclical intravenous treatment with pamidronate is of clinical benefit in children with
moderate to severe osteogenesis imperfecta (OI) types I, III and IV, but there is no …

Effects of intravenous pamidronate treatment in infants with osteogenesis imperfecta: clinical and histomorphometric outcome

CFJ Munns, F Rauch, R Travers… - Journal of bone and …, 2005 - academic.oup.com
Clinical and histomorphometric outcome was compared between children with OI who had
received pamidronate since infancy and age‐matched patients who had never received …

Update on the evaluation and treatment of osteogenesis imperfecta

J Harrington, E Sochett, A Howard - Pediatric Clinics, 2014 - pediatric.theclinics.com
Osteogenesis imperfecta (OI) is a term used to describe a group of inherited connective
tissue conditions that are characterized by increased bone fragility and low bone mass. With …

Bone mass, size, and density in children and adolescents with osteogenesis imperfecta: effect of intravenous pamidronate therapy

F Rauch, H Plotkin, L Zeitlin… - Journal of Bone and …, 2003 - academic.oup.com
Cyclical intravenous therapy with pamidronate improves the clinical course in children and
adolescents with osteogenesis imperfecta (OI). In this study, we evaluated the effect of this …

Osteogenesis imperfecta: advancements in genetics and treatment

V Rossi, B Lee, R Marom - Current opinion in pediatrics, 2019 - journals.lww.com
Osteogenesis imperfecta is a skeletal dysplasia characterized by bone fragility and
extraskeletal manifestations. Better understanding of the mechanisms of osteogenesis …

The spine in patients with osteogenesis imperfecta

MJ Wallace, RW Kruse, SA Shah - JAAOS-Journal of the …, 2017 - journals.lww.com
Osteogenesis imperfecta is a genetic disorder of type I collagen. Although multiple
genotypes and phenotypes are associated with osteogenesis imperfecta, approximately …

Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations

P Roschger, N Fratzl-Zelman, BM Misof… - Calcified tissue …, 2008 - Springer
Osteogenesis imperfecta type I (OI-I) represents the mildest form of OI. The collagen I
mutations underlying the disorder can be classified as quantitative mutations that lead to …

Genotype‐phenotype correlations in autosomal dominant osteogenesis imperfecta

IM Ben Amor, FH Glorieux, F Rauch - Journal of Osteoporosis, 2011 - Wiley Online Library
Osteogenesis imperfecta, discussed in Baldridge et al. 2008 is an inherited bone fragility
disorder with a wide range of clinical severity that in the majority of cases is caused by …

Skeletal effects and functional outcome with olpadronate in children with osteogenesis imperfecta: a 2-year randomised placebo-controlled study

R Sakkers, D Kok, R Engelbert, A van Dongen… - The Lancet, 2004 - thelancet.com
Background Non-randomised studies have suggested beneficial effects of bisphosphonates
in osteogenesis imperfecta. We assessed the effects of oral olpadronate in children with this …