Bone Abstracts

Contents

• Invited Speaker Abstracts
• • (1) (1)
  • • Fetal development

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    • Fetal development

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  • (1) (1)
  • • Bone and osteocyte biology: lessons from human genetic diseases

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    • Bone and osteocyte biology: lessons from human genetic diseases

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  • (1) (1)
  • • Bone material properties

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    • Bone material properties

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  • (1) (1)
  • • Vertebral fracture assessment

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    • Vertebral fracture assessment

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  • (1) (1)
  • • High resolution imaging of bones by high-resolution peripheral quantitative computed tomography

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    • High resolution imaging of bones by high-resolution peripheral quantitative computed tomography

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  • (1) (1)
  • • Classical osteogenesis imperfecta

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    • Classical osteogenesis imperfecta

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  • (1) (1)
  • • Recessive osteogenesis imperfecta

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    • Recessive osteogenesis imperfecta

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  • (1) (1)
  • • Early-onset osteoporosis

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    • Early-onset osteoporosis

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  • (1) (1)
  • • Upper limb deformity in osteogenesis imperfecta

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    • Upper limb deformity in osteogenesis imperfecta

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  • (1) (1)
  • • NF-1 bone biology and pseudoarthrosis

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    • NF-1 bone biology and pseudoarthrosis

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  • (1) (1)
  • • Recent advances in limb lengthening and deformity correction

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    • Recent advances in limb lengthening and deformity correction

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  • (1) (1)
  • • The role of TGF[beta] in high turnover bone diseases

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    • The role of TGF[beta] in high turnover bone diseases

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  • (1) (1)
  • • Shared therapeutic targets in genetic skeletal diseases

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    • Shared therapeutic targets in genetic skeletal diseases

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  • (1) (1)
  • • Somatic mosaic skeletal overgrowth disorders

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    • Somatic mosaic skeletal overgrowth disorders

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  • (1) (1)
  • • Achondroplasia-new therapy

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    • Achondroplasia-new therapy

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  • (1) (1)
  • • Growth plate and diseases of calcinosis

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    • Growth plate and diseases of calcinosis

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  • (1) (1)
  • • Molecular and cellular bases of high bone mass

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    • Molecular and cellular bases of high bone mass

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  • (1) (1)
  • • Management of sclerosing bone disease

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    • Management of sclerosing bone disease

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  • (1) (1)
  • • Rare sclerosing bone dysplasias

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    • Rare sclerosing bone dysplasias

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  • (1) (1)
  • • Bone morbidity in children with leukemia

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    • Bone morbidity in children with leukemia

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  • (1) (1)
  • • Cytokine- and steroid-induced osteoporosis

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    • Cytokine- and steroid-induced osteoporosis

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  • (1) (1)
  • • Anorexia nervosa

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    • Anorexia nervosa

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  • (1) (1)
  • • Multiphoton microscopy

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    • Multiphoton microscopy

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  • (1) (1)
  • • The new histology

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    • The new histology

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  • (1) (2)
  • • Beyond the mechanical in muscle-bone interaction

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    • Beyond the mechanical in muscle-bone interaction

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  • (1)
  • • Duchenne and cerebral palsy

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    • Duchenne and cerebral palsy

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• Oral Communications
• • (1)
  • • Abnormal trabecular micro-architecture and bone mechanical properties in adolescent idiopathic scoliosis: a case-control study with high-resolution peripheral quantitative computed tomography and finite element analysis

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    • Feature-based recognition of trabecular microstructure using 1.5T magnetic resonance imaging: a new methodology

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    • Sedentary time negates the positive influence of moderate-to-vigorous physical activity but not vigorous physical activity on bone strength in adolescent girls

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    • Increased bone matrix mineralization in treatment-naive children with Crohn's disease

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    • Bivariate analyses of BMD and lean mass in children identifies variants with novel pleiotropic effects across six BMD loci and in the TOM1L2 locus

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    • Early life motor control is positively associated with adolescent bone strength

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    • Osteogenesis imperfecta: a pilot trial on treatment with the RANKL-antibody denosumab

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    • Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfecta

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    • Skeletal manifestations in pediatric WNT1 osteoporosis

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    • Lack of PEDF within the bone matrix is associated with osteoidosis and abnormally high bone mineral content

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    • Comparison of RANKL blockade and bisphosphonate anti-resorptive therapies in a growing mouse model of OI: implications of prolonged treatment on bone health

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    • A zebrafish osteogenesis imperfecta model: a new tool to develop novel pharmacological treatments

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    • Meclozine has a potential effects on short stature and foramen magnum stenosis in transgenic mice with achondroplasia

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    • Small interfering RNAs as an innovative therapeutic approach for the autosomal dominant osteopetrosis type 2 (ADO2)

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    • Osseous side effects on the growing skeleton exerted by tyrosine kinase inhibitor treatment: data observed in pediatric patients with chronic myeloid leukemia in comparison to a juvenile rat model

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    • Medicarpin, a natural pterocarpan, enhances bone regeneration in cortical bone defect model by activation of notch and Wnt canonical signalling pathway

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    • Inhibition of TGF[beta] signalling delays ossification in patients with fibrodysplasia ossificans progressiva

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    • Improvement in bone manifestations and respiratory status in infants and young children with HPP treated with asfotase alfa: an update on the ENB-010-10 trial

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    • The VINE study: vitamin D in newborns: a randomized controlled trial comparing daily and bolus supplementation in breastfed infants of vitamin D deficient mothers

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    • The effect of calcium supplementation on adolescent bone growth in pre-pubertal Gambian females: a 12-year follow-up study

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    • Maternal vitamin D deficiency alters later skeletal responsiveness to mechanical loading in a model system

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    • Extra vitamin D from food fortification and bone fractures in adolescents: results from the D-tect study

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• Late Breaking Oral Communication Abstracts
• • (1)
  • • Maternal vitamin D depletion disrupts neonatal skeletal development in mice

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    • Recessive osteogenesis imperfecta caused by missense mutations in SPARC

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• Oral Posters
• • (1)
  • • Skeletal and bone material phenotype in recessive osteogenesis imperfecta due to a novel homozygous point mutation in TMEM38B

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    • Abstract unavailable

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    • Increase of preosteoclasts and secretion of PDGF-BB by inhibition of cathepsin K activity increases mouse bone mass during development

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    • Transplantation of culture-expanded bone marrow cells and platelet rich plasma in lower limb lengthening for short stature patients

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    • Osteoclast phenotype of giant multinucleated cells in cherubism may determine the disease aggressiveness

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    • Genetic variation is involved in impairment of bone mineral density in long-term adult survivors of childhood cancer

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    • Lessons from homocystinuria: Cystathionine beta-synthase as a novel marker for osteogenic differentiation of human mesenchymal stem cells

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    • Characterising the muscle-bone unit in children and adolescents with and without cystic fibrosis using novel imaging techniques and jumping mechanography

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    • Growth, body mass index, bone health and ambulatory status of boys with Duchenne Muscular Dystrophy treated with daily vs intermittent oral glucocorticoid regimen

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    • Does degree of adiposity influence upper limb fracture site in children?

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    • Optimal dose of calcium for treatment of nutritional rickets

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    • A non-invasive method for screening vitamin D insufficiency for adolescents using skin colourimetry

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• Poster Presentations
• • (1)
  • • Abstract unavailable

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    • The assessment of bone regulatory pathways in children with malignant bone tumors

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    • PHEX, DMP1 and FGF23 mutations in a Malaysian hypophosphatemic rickets patient

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    • Bone turnover markers and bone mineral density after 12-month weight loss therapy in obese children

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    • Vitamin D and decreased bone density in children

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    • Bisphosphonate treatment of melorheostosis: A case report

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    • History of meconium ileus affects bone health and body composition in young patients with cystic fibrosis

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    • Body composition profile of patients with Duchenne muscular dystrophy living in a country with the obesity epidemic

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    • Vitamin D supplementation can improve velocity of growth in children with vitamin D deficiency which are in treatment with RHGH for growth hormone deficiency

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    • Infantile Blount's disease: histopathologic changes in the proximal tibial metaphysis -- comparison between medial and lateral specimens

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    • Effects of bisphosphonate for the development of scoliosis in children with osteogenesis imperfecta

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    • Elevated plasma c-terminal fibroblast growth factor, but not intact FGF23 or soluble Klotho, is associated with left ventricular hypertrophy in pediatric chronic hemodialysis patients

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    • Galactosyltransferase-1 deficiency: a novel cause of bone fragility due to impaired proteoglycan synthesis

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    • Accuracy of parental recall of children's lifetime fracture prevalence: implications for investigation of childhood osteoporosis

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    • Fibrous dysplasia in McCune Albright syndrome; treatment and follow up

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    • Genotype in patients with osteogenesis imperfecta using a targeted exome sequencing: correlation with phenotype

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    • MRI features as surrogate markers of X-linked hypophosphatemic rickets activity

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    • A novel mutation in CYP24A1 gene in an infant with severe hypercalcemia and unique neurological presentation

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    • The role of body composition in the relationship between lifestyle factors and bone parameters of young children

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    • Bone mineral density in patients with autosomal recessive osteopetrosis after hematopoietic cell transplantation

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    • Efficacy of GH therapy in short patients affected hypochondroplasia

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    • Racing to better bone health! A 6-month calcium and vitamin D randomised controlled trial in young male jockeys

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    • Relationship of IGF1 and bone parameters in 7--16 year old apparently healthy Indian children

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    • Bone status of Indian children and adolescents with type 1 diabetes mellitus

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    • Sitting time has a stronger effect on bone than moderate plus vigorous activity

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    • Effects of running bike use on bone quality in non-ambulant children with cerebral palsy: a pilot study

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    • Bone mineral density and clinical outcome after intravenous bisphosphonate discontinuation in children with osteogenesis imperfecta

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    • Year-round cord blood vitamin D concentrations in women from diverse ethnical backgrounds in a Mediterranean area in Spain

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    • Type 1 diabetes mellitus may predispose to lower bone mineral density through lower osteoblast signaling from increased levels of Dickkopf-1

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    • Whole-body MR imaging as diagnostic tool in children with hereditary multiple osteochondromas

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    • Mineral metabolism in children with autosomal dominant polycystic kidney disease

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    • Characteristics of Malawian children undergoing corrective bone surgeries of rickets-like lower limb deformities

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    • In utero effects of iron status on infant fibroblast growth factor-23 and mineral metabolism

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    • Abstract unavailable

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    • Spinal muscular atrophy: another non-ambulatory population at risk for low bone mineral density

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    • Bone mineral density, pubertal status and ability to walk are associated to fracture incidence in patients with Rett syndrome

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    • Teriparatide following bisphosphonates in the treatment of osteoporosis in post-pubertal teenagers

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    • Serum 25-vitamin D level is lower in African American compared to Caucasian children

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    • Fracture and bone mineral density outcomes after bisphosphonate discontinuation in children with osteogenesis imperfecta treated with zoledronic acid compared to pamidronate

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    • Painful hip in 19-months old represents an intertrochanteric fracture following a low energy injury

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    • Percutaneously performed image-guided radiofrequency ablation for the treatment of a unifocal eosinophilic granuloma of the femur in a 16-year-old boy

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    • Levels of vitamin D according to severity of motor function disorder and the level of bone mineral density in children with cerebral palsy

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    • Efect of nutritional status on bone density in children with cerebral palsy

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    • Closed image-guided vs open biopsies in children with bone lesions: a retrospective review of 112 biopsies performed on 104 patients

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    • Skeletal dysplasia with short stature and a Larsen-like phenotype due to a homozygous mutation in B3GAT3

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    • Evaluation of the use of a dynamic elastomeric fabric orthosis to improve truncal stability in a young child with osteogenesis imperfecta

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    • Ethnic and gender differences in metacarpal dimensions in black and white South African children from pre-puberty through adolescence

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    • Bone mineral density, vertebral compression fractures and pubertal delay in patients with autosomal recessive epidermolysis bullosa

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    • Using high-resolution peripheral quantitative computed tomography (HRpQCT) to better understand the skeletal response to exercise

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    • ‘Double trouble': Duchenne muscular dystrophy and osteogenesis imperfecta in one patient - a case report

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    • Abstract unavailable

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    • Association of dietary calcium intake and body fat with hypertension in Indian adolescents

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    • Somatic COL1A1 mosaicism in a newborn with osteogenesis imperfecta

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    • Vitamin D overdose: Poor dosage guidelines for babies?

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    • Abstract unavailable

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    • Abnormal functional responses of osteoblasts to leptin in adolescent idiopathic scoliosis

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    • Fractures in infants - a population-based study over 15 years in Helsinki, Finland

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    • Music therapy as an avenue to promote healthy eating, exercise and bone health in children

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    • Vibration treatment can enhance the bioactive response of osteoblasts to vitamin D in adolescent idiopathic scoliosis patients

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    • Comparing two scanning protocols for high-resolution peripheral quantitative computed tomography for bone quality assessment in young subjects

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    • Association of vitamin D concentrations with 7-Dehydrocholesterol Reductase in school children in a sun-rich, semi-rural setting in Western Maharashtra, India

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    • Association of dental and skeletal fluorosis with calcium intake and vitamin D concentrations in adolescents from a region endemic for fluorosis

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    • Dietary calcium intake influences the relationship between serum 25 hydroxyvitamin D concentrations and Parathyroid hormone

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    • Peripubertal bone quality and density profile of Chinese adolescents in Hong Kong

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    • Results of a specialized rehabilitation approach in osteogenesis imperfecta

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    • Challenges in the management of hip dislocation a patient with Prader Willi syndrome

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    • McCune-Albright Syndrome in three patients, clinical correlation and spectrum of the disease

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    • Body composition and vertebral changes in children with osteogenesis imperfecta -- effect of risedronate

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    • A pilot study to evaluate the effectiveness of a group circuit therapy programme for children with osteogenesis imperfecta

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    • Ultrasonographic assessment of the skeletal development of the proximal tibia epiphysis, the proximal femur and the distal femur epiphysis in premature and mature newborns

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    • Muscle and bone impairment in children with Marfan syndrome: correlation with age and FBN1 genotype

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    • Vitamin D status in young women with anorexia nervosa during intensive weight gain therapy

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    • Long-term outcomes of surgical treatment for craniofacial fibrous dysplasia

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    • A case of resistant hypophosphataemic rickets

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    • To predict curve progression in newly diagnosed AIS girls -- how good can bone mineral density do?

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    • Bone quality in severe adolescent idiopathic scoliosis -- quantitative computed tomography of lumbar spine vs high-resolution peripheral quantitative computed tomography of the distal radius: a pilot study

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    • Vertebral fractures in children affected by chronic recurrent multifocal osteomyelitis: case reports and therapy response

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    • Bone metabolism in children and adolescents with newly diagnosed acute lymphoblastic leukemia

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    • Nonbacterial osteitis: Is there any mismatch in the pathophysiology of osteoblasts or osteoclasts?

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    • Ibandronate in the treatment of pediatric osteoporosis

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    • Liver growth hormone receptor signaling in chronic kidney disease related growth retardation: the role of suppressor of cytokine signaling 2

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    • Relationships among 25-hydroxyvitamin D, Parathyroid Hormone, and bone turnover markers in Chinese children

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    • RANKL, OPG, Dkk1 in Duchenne muscular dystrophy

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    • Different causes of infantile hypercalcemia

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    • Comparison of three detection assays of serum 25(OH) D

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    • Caries intensity and bone mineral density in children living in fluorine deficient region

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    • Influence of vitamin D deficiency on the bone mineral density in schoolchildren

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    • Vitamin D and bone health: A practical clinical guideline for management in children and young people in the UK

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    • Bone mineral density in solid cancer survivors: a cross sectional long-term follow-up study. A preliminary report

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    • Longitudinal bone development in patients with classical congenital adrenal hyperplasia: data using peripheral quantitative computed tomography

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    • Changes in the concentration of vitamin D in the course of intensive treatment of acute lymphoblastic leukemia. A preliminary data

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    • Risedronate in the treatment of children with osteogenesis imperfecta: retrospective review of practice and outcomes at a large paediatric metabolic bone unit

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    • Improving low bone mass in girls with adolescent idiopathic scoliosis (AIS) using calcium and vitamin D supplementation - a randomized controlled trial

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    • Effects of different socioeconomic conditions on bone mineral density in healthy Turkish female university students; relation with vitamin D status

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    • Osteomyelitis and septic arthritis in children: first data from the EUCLIDS network

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    • Bone health among boys with Duchenne muscular dystrophy before initiation of glucocorticoids

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    • Dysosteosclerosis from a unique mutation in SLC29A3

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    • Clinical predictors of low bone mineral density in children with juvenile idiopathic arthritis

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    • The role of vitamin D in growth physiology in early-aged and preschool children

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    • Secondary osteoporosis in boys with Alagille syndrome -- case report

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    • X-linked spinal muscular atrophy caused by de novo c.1731C>T substitution in the UBA1 gene

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    • Bone robusticity in two distinct skeletal dysplasias: an evaluation of the second metacarpal, a surrogate for bone strength

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    • Gait assessment in children with childhood hypophosphatasia: impairments in muscle strength and physical function

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    • Effect of intravenous pamidronate in the treatment of skin calcinosis in the course of juvenile dermatomyositis -- a story half-told

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    • Refractory hypercalcaemia of malignancy: responsiveness to Denosumab and Zoledronate

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    • Metatropic dysplasia is associated with increased fracture risk and increased markers of bone turnover

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    • Bone mineral density in Pelizaeus Merzbacher disease

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    • Unique occurrence of long bone fragility with cranial hyperostosis: Searching for the genetic culprit

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    • Effects of inorganic phosphate and FGF23 on C2C12 myoblast cells

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    • Abstract unavailable

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    • Is groupwork an effective way to improve transition for young people with osteogenesis imperfecta? A pilot study

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    • Type V osteogenesis imperfecta: confirmation of highly characteristic radiographic findings in early infancy

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    • Comparison of cost benefits and efficacy of Zoledronic acid and Pamidronate in the treatment of osteogenesis imperfecta in children

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    • Influence of pubertal development and body composition on bone mass accrual in apparently healthy school children aged 6-17 years

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    • Vitamin D and bone mineral density in children with Duchenne muscular dystrophy relation to fractures and ambulation status

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    • Osteopetrosis with uncommon final height: can only local IGF1 hold normal growth during pubertal spurt?

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    • Familial hypocalciuric hypercalcemia in two Chinese families -- common and uncommon features

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    • Changes in total body and regional bone mass in relation to body composition in children with osteogenesis imperfecta treated with pamidronate

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    • Burden of disease in children with hypophosphatasia: results from patient-reported surveys

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    • Fracture incidence and bisphosphonate therapy in boys with Duchenne Muscular Dystrophy

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    • A case of osteogenesis imperfecta mimicking the features of mucopolysaccharidosis IVA

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    • Phalangeal microgeodic disease: A rare cause of painful swollen toes

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    • Does the introduction of vertebral fracture assessment change clinical practice?

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    • Bisphosphonate treatment and the characteristics of femoral fractures in children with osteogenesis imperfecta

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    • Vitamin D status of gastrostomy-fed children with special needs

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    • Low bone mass in children with epidermolysis bullosa

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    • The outcomes of a standardized approach to managing metabolic bone disease of prematurity

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    • Patients treated with anti-epileptic drugs have a higher rate of fracture and impaired bone and muscle development compared with controls: results from a pilot study

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    • Cortical area and volumetric density during pubertal growth: longitudinal analysis in black and white South African adolescent males

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    • Chronic recurrent multifocal osteomyelitis: the value of whole-body MRI in a series of 34 children

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    • Association between serum 25-hydroxyvitamin D and incidence of infections in 6--12 years old children in a semi-rural setting in Western Maharashtra, India

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    • Bone structural characteristics and response to bisphosphonate treatment in children with Hajdu--Cheney syndrome

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    • Fibrodysplasia ossificans progressiva: disabling but now treatable

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    • Associations of 25-hydroxyvitamin D with major components of metabolic syndrome in children

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    • Chronic recurrent multifocal osteomyelitis in children: a new, MRI-based method of quantifying inflammation in the bone

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    • A modified performance-oriented mobility assessment tool for assessing clinically relevant gait impairments and change in children with hypophosphatasia: development and validation

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    • A slow and difficult diagnosis of a child with chronic recurrent multifocal osteomyelitis

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    • In-depth phenotyping including analyses of skin connective tissue in osteogenesis imperfecta

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    • Abstract unavailable

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    • Rickets in two patients pediatrics

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    • Persistence of musculoskeletal abnormalities in children and adolescents with inflammatory bowel disease: a prospective longitudinal study

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    • The mechanical multi-stimulation for musculoskeletal disease

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    • Low serum vitamin D levels in children treated for hematologic oncologic diseases

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    • Hypomagnesaemia due to lead poisoning in the context of a heterozygous CLDN-16 mutation

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    • Zoledronate as first line therapy for pediatric osteogenesis imperfecta?

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    • Hypovitaminosis D and factors associated in healthy children aged 2--14 years old in Mexico

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    • A severe form of cerebral palsy as a risk factor for the development of secondary osteoporosis in children

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    • Prevalence of vertebral fractures in survivors of childhood acute lymphoblastic leukemia

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    • Trabecular bone density decreased during 6 year observation in girls with Turner syndrome, but was not associated with fracture history

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    • Impaired bone mineral density in adult survivors of childhood cancer: a literature review

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    • Do children with mild to moderate osteogenesis imperfecta (OI) with abdominal muscle weakness have a higher incidence of pars defects? A physiotherapy pilot

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    • Syphilitic bone disease: a case report

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    • In-vivo high-resolution peripheral quantitative computer tomography assessment of skeletal microstructure in children with osteogenesis imperfecta

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    • A longitudinal, prospective, long-term registry of patients with hypophosphatasia

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    • Hydroxylase (CYP27B1) deficiency presenting with marked hypotonia, growth failure, hypoventilation, pulmonary hypertension and a renal proximal tubulopathy

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    • Children with coeliac disease on gluten free diet have normal bone mass, geometry and muscle mass

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    • Hypoxia inducible factor-1α directly induces the expression of receptor activator of nuclear factor-κB ligand in MLO-Y4 osteocytes

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    • Extreme, biomechanically-explained remodelling of biological femoral reconstructions in pediatric oncology

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    • The usefulness of bioelectrical impedance analysis in the proper assessment of nutritional status in children and adolescents with idiopathic scoliosis

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    • Prevalence of muscle deficits in survivors of childhood acute lymphoblastic leukemia

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    • Unusual adverse reaction of pamidronate: thrombophlebitis

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    • Abstract unavailable

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    • Whole blood gene expression analysis in idiopathic infantile hypercalcemia due to compound heterozygous mutation in the CYP24A1 gene in an Austrian 4-month-old boy and his family

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    • Effect of vitamin D supplementation on glucose metabolism, immune function and bone turnover in children with vitamin D deficiency

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    • Clinical masks of the tricho-rhino-phalangeal syndrome: based on the series of four cases from Poland

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    • The role of AMPK pathway in mediating the effects of metformin on mesenchymal stem cell differentiation

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    • Muscle power and force are predictors of bone microarchitecture and strength in healthy children and adolescents measured by high resolution peripheral quantitative computed tomography and jumping mechanography

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    • Ambulatory impairment and bone status in subjects with Rett Syndrome: a 10-year longitudinal study

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    • Comparison of the response to bisphosphonate treatment between acute lymphoblastic leukaemia and osteogenesis imperfecta type I

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    • Reduced spinal volumetric trabecular bone mineral density in adolescent girls with anorexia nervosa

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    • Bone-muscle unit assessment with pQCT in children with inflammatory bowel disease following treatment with Infliximab

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    • The possibilities of bone regeneration in children

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    • Papilledema in a toddler: An atypical presentation of X-linked hypophosphatemic rickets

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    • Case report of reversible cardiomyopathy secondary to 1 alpha hydroxylase deficiency

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    • Effect of baseline vitamin D status on serum 25(OH) D level and body composition in breastfed infants on vitamin D supplementation

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    • Evaluation of fibroblast growth factor 23 in patients with hypophosphataemic rickets

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    • Fractures in boys with Duchenne muscular dystrophy and their relationship to age

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    • The precision of partial image analysis of trabecular bone microarchitecture by high-resolution magnetic resonance imaging in people with childhood-onset bone abnormalities

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    • An atypical case of bone fragility and dysmorphism with an unusual and novel de novo COL1A1 mutation

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    • Rare diseases of bones, joints and vessels study

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    • Short stature in osteogenesis imperfecta: consider alternative diagnoses

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    • A case of moderate osteogenesis imperfecta with cerebral palsy spastic quadriplegia; an impossible combination, or is it?

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    • Deficits of vitamin D are strongly associated with methotrexate treatment in patients with juvenile idiopathic arthritis

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    • A subtrochanteric femoral stress fracture following bisphosphonate treatment in an adolescent girl

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    • The effect of iron chelators on bone health in patients with thalassemia

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    • Cole-Carpenter syndrome

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    • TBS increases over time in pre-teen girls

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    • Fractures, bone mass and geometry in black and white South African children: The Birth to Twenty cohort

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    • Two infants with the diagnosis of infantile hypophosphatasia: case report

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    • Bone quality and quantity in Duchenne Muscular Dystrophy patients

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    • Evolution of bone quality and quantity in patients suffering from Duchenne Muscular Dystrophy

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    • Low bone mineral density and fractures are prevalent in children with spinal muscular atrophy

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    • Aggravated bone density decline following symptomatic osteonecrosis in children with acute lymphoblastic leukemia

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    • Results of conservative treatment in patients with phosphate diabetes

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    • Increase of bone mineral density in patients with osteogenesis imperfecta treated with pamidronate disodium.

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    • Early onset cataract in an infant with activating calcium sensing receptor mutation

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    • Benign osteopetrosis associated with homozygous mutation in CLCN7

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    • Impaired mobility and pain significantly impact the quality of life of children with X-linked hypophosphatemia

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    • LRP5-associated high bone mass disorder: novel familial mutation in LRP5 and investigation of bone mineralization density distribution (BMDD)

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    • Relationship of lipid parameters and insulin resistance with bone health in South Korean adolescents

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    • The results of pamidronate treatment independently and in combination with surgery in patients with osteogenesis imperfecta.

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