Bone Abstracts

Contents

• Invited Speaker Abstracts
• • The fracturing child: epidemiology
  • • Bone mass and other determinants of fractures in children and adolescents

      ba0002is1
    • Bone mass and other determinants of fractures in children and adolescents

      ba0002is1biog
  • (1) (1)
  • • Epigenetic influences on childhood bone accrual

      ba0002is2
    • Epigenetic influences on childhood bone accrual

      ba0002is2biog
  • The fracturing child: biology
  • • Bone structure and fractures

      ba0002is3
    • Bone structure and fractures

      ba0002is3biog
  • (1) (1)
  • • The biology of bone revealed through bone biopsy

      ba0002is4
    • The biology of bone revealed through bone biopsy

      ba0002is4biog
  • Rare diseases
  • • Acrodysostosis

      ba0002is5
    • Acrodysostosis

      ba0002is5biog
  • (1) (1)
  • • Gaucher disease

      ba0002is6
    • Gaucher disease

      ba0002is6biog
  • (1) (1)
  • • Osteogenesis imperfecta

      ba0002is7
    • Osteogenesis imperfecta

      ba0002is7biog
  • The fracturing child: diagnostics
  • • Non-invasive assessment of bone structure and strength using QCT and MRI

      ba0002is8
    • Non-invasive assessment of bone structure and strength using QCT and MRI

      ba0002is8biog
  • (1) (1)
  • • DXA and vertebral fracture assessment

      ba0002is9
    • DXA and vertebral fracture assessment

      ba0002is9biog
  • The fracturing child: therapeutics
  • • Medical therapies: present and future

      ba0002is10
    • Medical therapies: present and future

      ba0002is10biog
  • (1) (1)
  • • Other therapeutic options: nutrition, vitamin D, and physical activity

      ba0002is11
    • Other therapeutic options: nutrition, vitamin D, and physical activity

      ba0002is11biog
  • Chronic diseases
  • • Bone mineral density and fractures in pediatric inflammatory bowel disease

      ba0002is12
    • Bone mineral density and fractures in pediatric inflammatory bowel disease

      ba0002is12biog
  • (1) (1)
  • • Muscle[ndash]bone interaction in pediatric bone diseases

      ba0002is13
    • Muscle-bone interaction in pediatric bone diseases

      ba0002is13biog
  • (1) (1)
  • • Chronic diseases: type I diabetes

      ba0002is14
    • Chronic diseases: type I diabetes

      ba0002is14biog
  • Paediatric cancer and bone: round table
  • • Osteogenic complications during and after childhood cancer

      ba0002is15
    • Osteogenic complications during and after childhood cancer

      ba0002is15biog
  • (1) (2)
  • • Fractures among long-term survivors of childhood cancer

      ba0002is16
    • Fractures among long-term survivors of childhood cancer

      ba0002is16biog
  • Obesity as a bone disease: round table
  • • Bone as an endocrine organ

      ba0002is17
    • Bone as an endocrine organ

      ba0002is17biog
  • (1)
  • • Obesity and skeletal health

      ba0002is18
    • Obesity and skeletal health

      ba0002is18biog
• Oral Communications
• • Epidemiology
  • • The Amalgamated Paediatric Bone Density Study (The ALPHABET Study): the collation and generation of UK based reference data for paediatric bone densitometry

      ba0002oc1
    • Fracture patterns and bone mass in South African adolescent-mother pairs: the Birth to Twenty Cohort

      ba0002oc2
    • Pediatric differences in bone mineral density according to ethnic background in children: The Generation R Study

      ba0002oc3
    • Maternal antenatal 25(OH)-vitamin D status is associated with offspring muscle strength at 4 years of age

      ba0002oc4
    • Novel musculoskeletal phenotypes during childhood for epidemiological studies

      ba0002oc5
    • Role of bone-associated loci identified in GWAS meta-analyses in the context of longitudinal pediatric BMD in European Americans

      ba0002oc6
  • Biology
  • • The PPP6R3/LRP5 locus influences lean mass in children of different ethnic background and highlights pleiotropic effects and muscle-bone interactions

      ba0002oc7
    • Generation of the first mouse model of autosomal dominant type II osteopetrosis harbouring the pG213R-clc7 mutation

      ba0002oc8
    • EPO signaling and hematopoietic expansion as causes of osteoporosis in a thalassemia mouse model

      ba0002oc9
    • Phenotypic dissection of bone mineral density facilitates the identification of skeletal site specificity on the genetic regulation of bone

      ba0002oc10
    • Connectivity map-based discovery of novel compounds that induce osteoblast differentiation

      ba0002oc11
    • Improvement of collagen synthesis in fibroblasts of Brtl model for osteogenesis imperfecta following lentiviral-shRNA-mediated down-expression of mutant Col1a1 allele

      ba0002oc12
  • Diagnostics
  • • Level of calcium intake modifies the correlation between parathyroid hormone and 25-hydroxyvitamin D: a proposal of adequate 25-hydroxyvitamin D levels in children

      ba0002oc13
    • What DXA measurement sites are best for bone health assessment in children? Effect of inter-machine differences on bone outcomes from the Bone Mineral Density in Childhood Study

      ba0002oc14
    • Bone health index: Swiss children have less in the bank than a generation ago

      ba0002oc15
    • Longitudinal analysis of volumetric density, size and strength towards the end of skeletal maturation in Gambian males habituated to low calcium intake

      ba0002oc16
    • Determinants of bone mineral density in long-term adult survivors of childhood cancer

      ba0002oc17
    • Trabecular bone score applied to normal children's lumbar spine DXA scans

      ba0002oc18
  • Miscellaneous
  • • New therapeutic approach in OI VI: suppression of bone resorption using the RANKL antibody denosumab

      ba0002oc19
    • Exercise completed when young provides lifelong benefit to cortical bone structure and estimated strength

      ba0002oc20
    • A randomized, double-blind, placebo-controlled trial of alendronate treatment for fibrous dysplasia of bone

      ba0002oc21
    • Prolidase deficient mice are osteoporotic in early life

      ba0002oc22
    • Switching from alendronate to RANKL blockade alters bone properties after 14 weeks of therapy in the oim/oim mouse

      ba0002oc23
    • Fibroblast Growth Factor 23 Plasma Levels Are Elevated with Early Chronic Kidney Disease and Positively Associated with Steroid Based vs Steroid Free Immunosuppression in Pediatric Renal Transplant Patients

      ba0002oc24
  • Chronic diseases
  • • Wnt/[beta]-catenin: a candidate pathway for bone repair in neurofibromatosis type-1

      ba0002oc25
    • Vertebral fractures in the 3-year period following steroid initiation among children with chronic illnesses

      ba0002oc26
    • Serum vitamin D level can affect the treatment outcome of whole-body vibration for low bone mass in girls with adolescent idiopathic scoliosis

      ba0002oc27
    • Bone mineral density at diagnosis determines fracture rate in children-treated according to the DCOG-ALL9 protocol

      ba0002oc28
    • Mineral metabolism, cortical volumetric bone mineral density and fracture risk in childhood chronic kidney disease

      ba0002oc29
    • Alteration of wnt/[beta]-catenin signaling in HIV-infected youths: a mechanism leading to impaired bone health?

      ba0002oc30
• Oral Posters
• • (1)
  • • Skeletal effects of hypothyroidism are mediated by thyroid hormone receptor [alpha]

      ba0002op1
    • High FSH serum levels may support the altered bone remodeling in Turner syndrome patients

      ba0002op2
    • Calcimimetics as adjunct therapy in XLH: 18 months experience

      ba0002op3
    • A new start-codon in IFITM5 causes osteogenesis imperfecta type V

      ba0002op4
    • Abstract unavailable

      ba0002op5
    • Children with nephrotic syndrome have increased tibial bone area but similar volumetric bone mineral density to healthy controls

      ba0002op6
    • Bone mineralization density distribution, bone formation rate and bone turnover markers in a cohort of children with CKD before and after GH treatment

      ba0002op7
    • Quantitative measurement of abnormal bone quality and strength with bone micro-architecture and rod-plate configuration in osteopenic adolescent idiopathic scoliosis

      ba0002op8
    • Anticalciuric effect of recombinant PTH in patients with activating mutations of the calcium-sensing receptor causing autosomal dominant hypocalcaemia--hypercalciuria

      ba0002op9
    • Metacarpal width, length, medullary diameter and cortical thickness in hypophosphatemic rickets

      ba0002op10
    • Artistic gymnasts display micro-architectural advantages over trampolining and tumbling gymnasts: a high resolution peripheral quantitative computed tomography study

      ba0002op11
    • The bone/vessels interplay in teenagers with chronic kidney disease

      ba0002op12
    • Long-term effects of bisphosphonate therapy in children with osteogenesis imperfecta

      ba0002op13
    • Inflammation and glucocorticoid therapy impair skeletal modeling during growth following crohn disease diagnosis

      ba0002op14
    • Dissecting the role of osteoblast derived nitric oxide in bone remodeling

      ba0002op15
• Poster Presentations
• • (1)
  • • Abstract unavailable

      ba0002p1
    • Abstract unavailable

      ba0002p2
    • Abstract unavailable

      ba0002p3
    • Abstract unavailable

      ba0002p4
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical and molecular genetic findings

      ba0002p5
    • The relationship between bone health and body composition profile in patients with galactose metabolic disorders: implications for practice

      ba0002p6
    • Osteometric parameters of mature rats mandible molars when implanted in the tibia biogenic hydroxyapatite, saturated with iron

      ba0002p7
    • Compound heterozygosity of two functional null mutations in the ALPL gene associated with deleterious neurological outcome in an infant with hypophosphatasia

      ba0002p8
    • A 6-month intervention study with vibration therapy in severely disabled children: effects on bone, biochemical markers and acceptance

      ba0002p9
    • Osteoporosis in young patients with neurological impairments

      ba0002p10
    • Abstract unavailable

      ba0002p11
    • DXL measurements in children 2-10 years

      ba0002p12
    • Bone turnover compensates for the delayed growth in small for gestational age neonates

      ba0002p13
    • Bone status and body composition analysis in young patients with phenylketonuria and hyperphenylalaninemia

      ba0002p14
    • Osteogenesis imperfecta-bone mass acquisition under bisphosphonates treatment and additional gain in BMD in time of rhGH treatment for growth delay

      ba0002p15
    • Bone size and bone mineral content in adolescents and young adults with eating disorders

      ba0002p16
    • The optimal dose of vitamin D in growing girls during academic years: a randomized trial

      ba0002p17
    • Influence of anthropometric parameters on assessment of paediatric bone mineral density and bone mineral content

      ba0002p18
    • Positive correlation of serum vitamin D status with bone density and bone quality among adolescent girls in Hong Kong

      ba0002p19
    • Assessment of vitamin D nutrition status and dietary calcium intake in children 2-5 years of age

      ba0002p20
    • Bone disease in children with geroderma osteodysplasticum: a 25-year experience from a single tertiary centre

      ba0002p21
    • Association of volumetric bone mineral density, bone morphometry and trabecular bone micro-architecture with leptin and soluble leptin receptor in adolescent idiopathic scoliosis

      ba0002p22
    • Drop in allograft function associates with drop in bone mineral density Z-score in pediatric renal transplant recipients

      ba0002p23
    • Effects of endurance training on somatic growth in a rat model of chronic kidney disease related growth retardation

      ba0002p24
    • Maternal bone density and rickets in Nigerian children

      ba0002p25
    • Improvement in genu valgus deformity in hypophosphatemic rickets due to primary de Toni-Debre-Fanconi syndrome treated with phosphate, calcitriol and alkali therapy

      ba0002p26
    • Randomized-controlled study in kidney transplanted children: early corticoids withdrawal and effect on bone health recovery

      ba0002p27
    • Vitamin D insufficiency and its correlation with low bone mass in adolescent idiopathic scoliosis

      ba0002p28
    • Coping with osteogenesis imperfecta; what kind of difficulties are families living with?

      ba0002p29
    • The effect of psychoeducation in families with osteogenezis imperfecta

      ba0002p30
    • Craniofacial consequences of high dose zoledronic acid injections in onco-pediatric patients

      ba0002p31
    • The effect of vitamin D supplementation on calcium excretion in thalassemia

      ba0002p32
    • Patients with mutations in PHEX or FGF23 share FGF23 excess but present distinct bone and mineral metabolism features

      ba0002p33
    • Reliability of pQCT scan protocol of second metatarsal for children with juvenile idiopathic arthritis

      ba0002p34
    • Six-monthly i.v. zoledronic acid in childhood osteoporosis

      ba0002p35
    • Vitamin D deficiency and its relationship to parathyroid hormone in morbidly obese adolescents prior to bariatric surgery

      ba0002p36
    • Reduction in bisphosphonate side effect profile using short-term steroid cover

      ba0002p37
    • Abnormal bone quality in both cortical and trabecular compartments in adolescent idiopathic scoliosis

      ba0002p38
    • Prevalence of vitamin D deficiency in adolescent Muslim girls attending a school in the UK, which adheres to a conservative dress code

      ba0002p39
    • Altered bone metabolism in obese children: the pathogenic role of adipocytokines and inflammation

      ba0002p40
    • Management of a new case of neonatal hypocalciuric hypercalcemia related to mutation of the calcium-sensing receptor gene with bone abnormalities

      ba0002p41
    • The effect of glucocorticoids on bone indices in children with rheumatic and oncological conditions

      ba0002p42
    • Bone quality in young thalassaemic patients

      ba0002p43
    • A homozygous mutation in the DNA binding domain of human vitamin D receptor causes vitamin D resistant rickets

      ba0002p44
    • Bone mineral density impairment in marfan syndrome: a hidden and neglected issue

      ba0002p45
    • Interactions of adipokines and bone metabolism in patients with severe juvenile idiopathic arthritis

      ba0002p46
    • Vitamin D deficiency and structural and functional state of bone tissue in schoolchildren of Ukraine

      ba0002p47
    • Pubertal induction with testosterone of a boy with bilateral anorchia guided by the development of his monozygotic twin brother

      ba0002p48
    • Some features of regulation of the bone tissue metabolisms at the newborns who have transferred infectious influence during intrauterine development

      ba0002p49
    • Bioelectrical impedance as a screening tool for low bone mass in Indian children and adolescents

      ba0002p50
    • Mild visual impairment in a 13-year-old child with osteoporosis-pseudoglioma syndrome

      ba0002p51
    • Incidence of fractures in 2-18 years old affluent Indian children: a multicentre study

      ba0002p52
    • The influence of anthropometry and body composition on children's bone health the Childhood Health, Activity and Motor Performance School (The CHAMPS) study, Denmark

      ba0002p53
    • Association of calcium and dairy intake with growth in Indian children

      ba0002p54
    • Body composition, anthropometric parameters and bone densitometry in young Ukrainian male

      ba0002p55
    • Effect of puberty on the muscle-bone relationships in Indian children and adolescents

      ba0002p56
    • Heterozygous mutation in GALNT3 in a case of hyperphosphataemic familial tumoral calcinosis

      ba0002p57
    • Puberty is critical for the development of bone mineral density impairment in patients with congenital adrenal hyperplasia

      ba0002p58
    • The rapid effect of vibration on bone formation and resorption in the growing skeleton

      ba0002p59
    • Failure of free, public vitamin D supplementation program for Quebec infants: temporal trends and significant predictors

      ba0002p60
    • Elevated FGF23 levels in premature infants without excessive phosphaturia

      ba0002p61
    • The effect of the ketogenic diet on the developing skeleton

      ba0002p62
    • Bone status of Indian children and adolescents with type 1 diabetes mellitus

      ba0002p63
    • The level of vitamin D and calcium in urban pregnant women in Russian Federation

      ba0002p64
    • Improvement in morphological properties of trabecular bones and longitudinal growth in tibia for growing rats through an impact stimulation

      ba0002p65
    • Effect of resistance training on peripheral bone mineral density and muscle strength in adolescents with motor difficulties

      ba0002p66
    • Dual-energy X-ray absorptiometry in predicting clinical bone disease in adults with childhood onset end-stage renal disease

      ba0002p67
    • Engineered tridimensional hydroxyapatite scaffold to support bone resorption

      ba0002p68
    • sRANKL/OPG in children with idiopathic hypercalciuria

      ba0002p69
    • Isolated bilateral zeugo-autopodal segments agenesis of the lower limb: unusual malformation case report

      ba0002p70
    • The microarchitecture of bone in osteochondromas

      ba0002p71
    • Abstract unavailable

      ba0002p72
    • Histomorphometric parameters of the alveolar ridges of the mandible in immature rats after thymectomy

      ba0002p73
    • Assessment of bone mass and bone metabolism in children with chronic inflammatory bowel diseases

      ba0002p74
    • Vitamin D receptor gene Fok1 polymorphism and bone mass accrual in Indian girls

      ba0002p75
    • Final height and bone health in young adults, transplanted in childhood

      ba0002p76
    • A novel mutation in CRTAP gene in a patient with severe ostegenesis imperfecta type VII

      ba0002p77
    • Variable relationship of fat mass and bone with pubertal staging in obese and normal weight Indian children and adolescents

      ba0002p78
    • High sedentary lifestyle practices has adverse influence on musculoskeletal health in adolescent boys and girls: findings from a population-based study in Malaysia

      ba0002p79
    • Osteogenesis imperfecta and short stature: effect of sclerostin antibody treatment in oim/oim mice

      ba0002p80
    • Reference point indentation testing detects age-related changes in tissue mechanical properties in mice

      ba0002p81
    • The influence of sclerostin serum levels on bone mineral density and body composition in patients with Rett syndrome and healthy adolescent girls

      ba0002p82
    • Anti-RANKL nanobody ALX-0141 shows sustained biomarker inhibition in a phase I study in healthy postmenopausal women

      ba0002p83
    • Comparison of socioeconomic status on bone mass assessed by quantitative ultrasound of hand phalanges of boys from 7 to 15 years old

      ba0002p84
    • Comparison of socioeconomic status on bone mass assessed by quantitative ultrasound of the phalanges in girls from 7 to 15 years old

      ba0002p85
    • Assessing bone quality and fracture resistance in children using microindentation

      ba0002p86
    • Serum homocysteine levels in children and adolescents with impaired bone health

      ba0002p87
    • Children and adolescents with cystic fibrosis have normal volumetric BMD and geometry at the radius, but low muscle area at the forearm

      ba0002p88
    • Painful vertebral fractures during pregnancy: be aware of a potentially underlying genetic cause

      ba0002p89
    • Intravenous pamidronate in the treatment of severe idiopathic infantile hypercalcemia

      ba0002p90
    • Hypovitaminosis D in chronically ill children in Greece and its management

      ba0002p91
    • Bone mineralization in children with chronic gastroduodenitis

      ba0002p92
    • Long term efficacy of low dose pamidronate treatment in osteogenesis imperfecta and its effects on growth

      ba0002p93
    • Bone anomalies in Noonan syndrome

      ba0002p94
    • Abstract unavailable

      ba0002p95
    • Cross-sectional associations of sex steroids with bone maturation, bone mineral density and bone geometry in boys

      ba0002p96
    • Vitamin D status and bone health in survivors of childhood lymphoblastic leukemia

      ba0002p97
    • Effects of denosumab on bone biochemistry and calcium metabolism in a girl with Juvenile Paget's disease

      ba0002p98
    • Potential association between vitamin D deficiency and hypertension in adolescents: a Pilot study

      ba0002p99
    • Preliminary evidence of reduced volumetric trabecular bone mineral density in children with idiopathic hypercalciuria: a peripheral quantitative computed tomography study

      ba0002p100
    • Rapid bone mass recovery after parathyroidectomy for primary hyperparathyroidism in a 15-year-old boy

      ba0002p101
    • Influence of nutritional status in the bone mass assessed by quantitative ultrasonography of boys

      ba0002p102
    • Celiac disease and bone disorders: diagnosis age influence

      ba0002p103
    • Immunohistochemical localization of bone morphogenetic proteins and their receptors in human osteochondromas

      ba0002p104
    • Bisphosphonate treatment in non-ambulatory patients with spastic quadriplegic cerebral palsy and other neuromuscular disorders: effectiveness of pamidronate vs zoledronic acid

      ba0002p105
    • Acquired hypophosphatemic rickets in a 13-year-old boy presenting with knee pain and valgus deformity

      ba0002p106
    • Bone cross-sectional geometry and volumetric density at the distal radius in female adolescents with anorexia nervosa

      ba0002p107
    • Antenatal glucocorticoid injections do not aggravate stress-induced bone loss in young adult mice

      ba0002p108
    • Vertebral morphology assessment in children: can a modified algorithm-based qualitative technique be used reliably?

      ba0002p109
    • Replacing conventional spine radiographs with dual energy X-ray absorptiometry in children with suspected reduction in bone density

      ba0002p110
    • Vitamin D status and association to bone health in 781 healthy 8-11 years old Danish school children: preliminary results from the Opus school meal study

      ba0002p111
    • Abstract unavailable

      ba0002p112
    • Everyday chemicals modulate bone properties during development

      ba0002p113
    • Association between parameters of bone mass measured by dual energy X-ray absorptiometry and quantitative ultrasound of proximal phalanges in children and adolescents with congenital adrenal hyperplasia

      ba0002p114
    • Bone mineral density in late adolescence of transsexuals treated with GnRH-analogues in their teens

      ba0002p115
    • Vitamin D dependent rickets type 1: 2 years after discontinuation of treatment

      ba0002p116
    • Impact of age and pubertal development on bone mass assessed by quantitative ultrasound of the proximal phalanges in boys and girls aged 10-14 years

      ba0002p117
    • Variation in response to vitamin D therapy in a series of consecutive children referred to a paediatric bone disease service

      ba0002p118
    • Depressive symptoms and bone mineral density in a cohort of portuguese adolescents: no association

      ba0002p119
    • Osteoblasts communicate with their neighbouring cells via extracellular vesicles

      ba0002p120
    • Tibial metaphyseal shape varies between children according to history of fracture

      ba0002p121
    • Fasting total ghrelin levels are increased in patients with adolescent idiopathic scoliosis

      ba0002p122
    • Inadequately treated hypophosphataemic rickets in 14-year-old boy: a case report

      ba0002p123
    • Adipokines and bone turnover throughout adolescence: an exploratory approach in a cohort of girls

      ba0002p124
    • Growth plate modifications in lysophosphatidic acid LPA1 receptor-invalidated mice

      ba0002p125
    • The role of severity of GH deficiency on clinical and instrumental features and response to treatment in children

      ba0002p126
    • Mechanosensitive TRP channels are essential for Ca2+ signaling in osteoclastogenesis

      ba0002p127
    • Bone mineral density in survivors of childhood lymphoma

      ba0002p128
    • Radiographic evidence of rapid healing of vitamin D deficient rickets after 2 weeks of therapy

      ba0002p129
    • 'Bone in bone' sign in juvenile osteoporosis in a 13-year-old girl

      ba0002p130
    • Ghrelin differentiates human osteoblasts via GHS-R1a receptor

      ba0002p131
    • Studies on bone and osteoclasts in patients with Shwachman Diamond syndrome

      ba0002p132
    • Linear growth over 2 years of velaglucerase alfa therapy in children with type 1 Gaucher disease previously treated with imiglucerase

      ba0002p133
    • Cessation of ambulation results in a dramatic loss of trabecular bone density in boys with Duchenne muscular dystrophy

      ba0002p134
    • Is vertebral fracture assessment by DXA more useful in a high fracture risk paediatric population than in a low-risk screening population?

      ba0002p135
    • Time to low bone mass occurrence in children diagnosed with acute lymphoblastic leukemia

      ba0002p136
    • Influence of nutritional status in the bone mass assessed by phalangeal quantitative ultrasound of girls aged 7-10 years old

      ba0002p137
    • Rare mutations associated with osteoclast-poor osteopetrosis provide molecular insights into receptor activator of NF[kappa][beta] signalling

      ba0002p138
    • How to cope with a case of heterotopic ossifications

      ba0002p139
    • Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal collagen I

      ba0002p140
    • Novel splicing mutation in FKBP10 gene in a patient with moderate/severe form of osteogenesis imperfecta

      ba0002p141
    • A case of geleophysic dysplasia

      ba0002p142
    • Fractures in juvenile idiopathic arthritis children: role of disease activity and genetic factors

      ba0002p143
    • Long-term bone sequelae following severe meningococcal septicaemia

      ba0002p144
    • The recurrent IFITM5 c.-14C>T transition which causes osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide: a novel mutational hot-spot?

      ba0002p145
    • A case of familial cherubism

      ba0002p146
    • A case of Gorham-Stout syndrome with chylothorax

      ba0002p147
    • Low bone mineral density in a group of girls with Rett syndrome

      ba0002p148
    • Bone mineral content in healthy danish children assessed by DXA-scanning and by computerised determination from hand radiographs

      ba0002p149
    • Markers of bone turnover in obese children: relationship to the nutritional status and oxidative stress level

      ba0002p150
    • Severity of spine deformity in children and adolescents with idiopathic scoliosis is associated with nutritional status and body composition

      ba0002p151
    • Zinc supplementation improves bone density in young adults with thalassemia

      ba0002p152
    • Low urinary citrate: a risk factor for fragility fractures in children and adolescents

      ba0002p153
    • Smad4 regulates growth plate chondrocyte proliferation, columnar organization and proteoglycan synthesis

      ba0002p154
    • Assessment of bone density in MPS IV (Morquio disease)

      ba0002p155
    • Reflection analysis of infant scans results may improve infant DXA bone density and body composition result that contain motion

      ba0002p156
    • Growth and bone health after hematopoietic stem cell transplantation or tyrosine kinase inhibitors in children with chronic myeloid leukemia: a single institution experience

      ba0002p157
    • Exploring vertebral abnormalities in patients with thalassemia and sickle cell disease

      ba0002p158
    • Novel SLC34A3 mutation causing mild hypophosphataemia, hypercalciuria and nephrolithiasis but no clinical or radiological evidence of rickets

      ba0002p159
    • A familial case of osteogenesis imperfecta: study of genotype-phenotype correlation

      ba0002p160
    • Autoimmune hepatitis and bone density in children

      ba0002p161
    • Low bone mass and fractures in young patients with chronic diseases

      ba0002p162
    • Phenotype-genotype correlation and role of ancillary investigations in atypical and rare forms of osteogenesis imperfecta

      ba0002p163
    • Vitamin D deficiency in Moscow children and adolescents

      ba0002p164
    • Morquio disease in two sisters: clinical case

      ba0002p165
    • Severe metabolic bone disease of prematurity following continuous veno-veno haemofiltration

      ba0002p166
    • Recurrent fractures and low bone mass in a patient with new mutation of LRP5 gene

      ba0002p167
    • Osteogenesis imperfecta: diagnostic difficulties due to clinical symptoms diversity: the results of own studies

      ba0002p168
    • Milk, childhood and postmenopausal osteoporosis

      ba0002p169
    • Achondroplasia: medical and orthopedic management in a pediatric patient

      ba0002p170
    • Vitamin D levels and signs of metabolic bone disease in adolescents with idiopathic scoliosis

      ba0002p171
    • Longitudinal assessment of spinal bone mineral density in children with neurofibromatosis type 1 using dual energy absorptiometry and quantitative computed tomography

      ba0002p172
    • Vitamin D prescription: a review of British National Formulary for children recommendations, and a proposal

      ba0002p173
    • Elite child athlete is our future: bone lumbar spine adaptation in Egyptian children monofin athletes

      ba0002p174
    • Correlation analysis of bone vibration frequency and its mass:volume ratio

      ba0002p175
    • One case of pseudohypoparathyroidism, clinical characterisation, follow-up and treatment

      ba0002p176
    • The bone mineral density of children with CF

      ba0002p177
    • Hypomagnesaemia with hypercalciuria secondary to mutations in the Claudin gene: a single-centre experience

      ba0002p178
    • The impact of selective serotonin reuptake inhibitors on bone mineral density in the pediatric and young adult population

      ba0002p179
    • Beyond brittle bones: a preliminary report from the osteogenesis imperfecta adult natural history initiative

      ba0002p180
    • Long-term imiglucerase/alglucerase treatment in Latin American children with type 1 Gaucher disease: lessons from the International Collaborative Gaucher Group (ICGG) Gaucher Registry

      ba0002p181
    • Reference curves for bone health index for Han children from five large cities in China, and a comparison to Asian-American children

      ba0002p182
    • Juvenile idiopathic osteoporosis: a case study

      ba0002p183
    • High FGF23 measurements in a child with vitamin D dependent rickets type I: cause or consequence?

      ba0002p184
    • An unusual presentation of progressive osseous heteroplasia in a 7-year-old female child

      ba0002p185
    • Bone mass, bone microarchitecture and anthropometric measurements during childhood growth in Spanish girls

      ba0002p186
    • Juvenile idiopathic osteoporosis responsive to intravenous alendronate

      ba0002p187
    • Abstract unavailable

      ba0002p188
    • Clinical features of temporary brittle bone disease

      ba0002p189
    • Vitamin D deficiency rickets in neonates

      ba0002p190
    • Long-term follow-up in Stuve-Wiedemann syndrome: a case report

      ba0002p191
    • The assessement of the vitamin D supply in the population of polish children at the age of 9-12 years: multicentre research: preliminary report

      ba0002p192
    • The effect of levothyroxine therapy on vitamin D and bone mineral density

      ba0002p193
    • Celiac disease underlying rickets in an adolescent

      ba0002p194
    • A case of progressive generalised osteolysis: a fibrous dysplasia or something else?

      ba0002p195
    • Bigger but not stronger? GH treatment in Turner syndrome may confer no benefit to HR-pQCT determined bone micro-architecture

      ba0002p196
    • Parathyroid hormone administered by continuous s.c. infusion is more effective than when given by intermittent injection

      ba0002p197
    • Severe hypercalcemia in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene

      ba0002p198
    • Levels of 25(OH)vitamin D in children and adolescents with type 1 diabetes mellitus and in healthy controls in Bulgarian population

      ba0002p199
    • Abstract unavailable

      ba0002p200
    • Guided growth with hinge plates for lack of extension and fixed flexion of the knee

      ba0002p201
• Late Breaking Abstracts
• • (1)
  • • Influence of age and gender on spine bone density and TBS microarchitectural texture parameters in infants

      ba0002lb1
    • WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta identify a key WNT ligand regulating bone mass

      ba0002lb2