Searchable abstracts of presentations at key conferences on calcified tissues
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Volume 6
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ICCBH2017
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8th International Conference on Children's Bone Health
All volumes
0007 ICCBH2019
0006 ICCBH2017
0005 ECTS2016
0004 ICCBH2015
0003 ECTS2014
0002 ICCBH2013
0001 ECTS2013
Summary
Abstract Book
Programme
Volume Editors
Abstracts
Contents
Poster List
(1)
Poster List
ba0006pl1
Invited Speaker Abstracts
(1) (1)
IS01
ba0006is01
IS01
ba0006is01biog
(1) (1)
Highlights in clinical bone research
ba0006is02
Highlights in clinical bone research
ba0006is02biog
(1) (1)
Bone cells in health and disease
ba0006is03
Bone cells in health and disease
ba0006is03biog
(1) (1)
Cortical bone structure and material properties
ba0006is04
Cortical bone structure and material properties
ba0006is04biog
(1) (1)
Skeletal mineralization - enzymes and animal models
ba0006is05
Skeletal mineralization - enzymes and animal models
ba0006is05biog
(1) (1)
The mechanobiology of the growing skeleton
ba0006is06
The mechanobiology of the growing skeleton
ba0006is06biog
(1) (1)
A role for leptin as a myokine mediating muscle-bone interactions
ba0006is07
A role for leptin as a myokine mediating muscle-bone interactions
ba0006is07biog
(1) (1)
Next generation sequencing and genome editing, game changers in the field of skeletal research
ba0006is08
Next generation sequencing and genome editing, game changers in the field of skeletal research
ba0006is08biog
(1) (1)
Skeletal dysplasia
ba0006is09
Skeletal dysplasia
ba0006is09biog
(1) (1)
Arterial calcification syndromes: causes and treatments
ba0006is10
Arterial calcification syndromes: causes and treatments
ba0006is10biog
(1) (1)
IS11
ba0006is11
IS11
ba0006is11biog
(1) (1)
The ERNS as a tool for the European research on rare diseases
ba0006is12
The ERNS as a tool for the European research on rare diseases
ba0006is12biog
(1) (1)
Osteoporosis in boys with Duchenne muscular dystrophy: morbidity, mechanisms and the path forward
ba0006is13
Osteoporosis in boys with Duchenne muscular dystrophy: morbidity, mechanisms and the path forward
ba0006is13biog
(1) (1)
Bone, body composition and metabolic abnormalities after allogeneic hematopoietic stem cell transplantation during childhood
ba0006is14
Bone, body composition and metabolic abnormalities after allogeneic hematopoietic stem cell transplantation during childhood
ba0006is14biog
(1) (1)
Bone in chronic kidney diseases: a systemic problem
ba0006is15
Bone in chronic kidney diseases: a systemic problem
ba0006is15biog
(1) (1)
Body composition and physical activity
ba0006is16
Body composition and physical activity
ba0006is16biog
(1) (1)
Factors influencing peak bone mass
ba0006is17
Factors influencing peak bone mass
ba0006is17biog
(1) (1)
Phosphate and FGF23 signaling
ba0006is18
Phosphate and FGF23 signaling
ba0006is18biog
(1) (1)
Signalling pathways and their significance for bone health and disease. PTH/cAMP/PKA
ba0006is19
Signalling pathways and their significance for bone health and disease. PTH/cAMP/PKA
ba0006is19biog
(1) (1)
Canonical Wnt signaling in bone health and disease
ba0006is20
Canonical Wnt signaling in bone health and disease
ba0006is20biog
(1) (2)
BOOSTB4: Boost Brittle Bones Before Birth A clinical trial on pre- and/or postnatal stem cell transplantation for treatment of osteogenesis imperfecta
ba0006is21
BOOSTB4: Boost Brittle Bones Before Birth A clinical trial on pre- and/or postnatal stem cell transplantation for treatment of osteogenesis imperfecta
ba0006is21biog
(1)
Role of microRNAs in the development of osteosarcoma
ba0006is22
Role of microRNAs in the development of osteosarcoma
ba0006is22biog
Oral Communications
(1)
NBAS variants causing a novel form of inherited bone fragility
ba0006oc1
Methylation patterns at the novel DMR of GNAS (GNAS-AS2) in pseudohypoparathyroidism 1B (PHP1B or iPPSD3) subtypes
ba0006oc2
Principal component-derived bone density phenotypes and genetic regulation of the pediatric skeleton
ba0006oc3
25-hydroxyvitamin D response to antenatal cholecalciferol supplementation is associated with common vitamin D related genetic variants: findings from the MAVIDOS trial
ba0006oc4
Eight-year longitudinal analysis of physical activity and bone strength during adolescence: The Iowa Bone Development Study
ba0006oc5
Lean mass accretion increases during summer and positively associates with vitamin D status in healthy children 2-8 years
ba0006oc6
The effect of antenatal iron supplementation on fibroblast growth factor-23 concentration in mothers and infants: a randomised controlled trial in rural Kenya
ba0006oc7
Effective therapeutic control of curve progression using calcium and vitamin D supplementation for adolescent idiopathic scoliosis - a randomized double-blinded placebo-controlled trial
ba0006oc8
Calcium carbonate supplementation of pregnant rural Gambian mothers alters offspring IGF-1 at age 7.5 years in a sex-dependent manner
ba0006oc9
Inadequate vitamin D status adversely affects trabecular bone mineral density in 14-18 year old adolescents
ba0006oc10
The effect of whole body vibration training on bone and muscle function in children with osteogenesis imperfecta and limited mobility: a randomized controlled pilot trial
ba0006oc11
Fracture incident rate and growth in a nationwide cohort of boys with Duchenne Muscular Dystrophy
ba0006oc12
Enterococccus faecium abundance in gut microbiome is associated with higher bone mineral density in school age children
ba0006oc13
Body composition and associated biomarkers as determinants of bone mineral density in children 6-8 years of age - The Physical Activity and Nutrition in Children (PANIC) study
ba0006oc14
Fractures in school age children in relation to sex, ethnic background and bone mineral density: the generation R Study
ba0006oc15
Pediatric hypophosphatasia - a retrospective single-center chart review of 50 children
ba0006oc16
Vertebral Fractures in children with chronic inflammatory and/or disabling conditions: the SNAP study
ba0006oc17
Stimulation of angiogenesis and osteogenesis by enhanced preosteoclast platelet derived growth factor type BB attenuates glucocorticoid-induced osteoporosis in growing mice
ba0006oc18
Mesenchymal stromal stem cells in pediatric orthopedic oncology, focus on osteosarcoma
ba0006oc19
Autoimmune hyperphosphatemic tumoral calcinosis
ba0006oc20
Scoliosis in fibrous dysplasia/McCune-albright syndrome
ba0006oc21
Type I collagen C-propeptide cleavage deficiency increases bone mineralization and alters bone cell differentiation
ba0006oc22
Sustained radiographic and functional improvements with asfotase alfa treatment from up to 7 years in children with hypophosphatasia
ba0006oc23
KRN23 effects on phosphate and vitamin D dysregulation in children <5 years old with X-Linked Hypophosphatemia (XLH)
ba0006oc24
Biochemical and physical function outcomes after 5 years of treatment with asfotase alfa in adolescents and adults with hypophosphatasia: phase 2 study results
ba0006oc25
A randomized, open-label Phase 2 study of KRN23, an investigational fully human Anti-FGF23 monoclonal antibody, in children with X-linked Hypophosphatemia (XLH)
ba0006oc26
Poster Presentations
(1)
Abstract unavailable
ba0006p001
A 3-year longitudinal study of skeletal effects and growth in children after kidney transplantation
ba0006p002
Abstract unavailable
ba0006p003
Bone mass tracks into teenage years
ba0006p004
Muscular fitness, bone mineral density and hip geometry in young males: the PRO-BONE study
ba0006p005
Bone density and body composition in post-pubertal adolescents treated with GnRH analogues in a gender identity development service
ba0006p006
Effects of a 8-month physical activity and nutrition-induced weight loss program on bone health of obese adolescents.
ba0006p007
Cardiorespiratory fitness, bone mineral density and hip geometry in young males: the PRO-BONE study
ba0006p008
Sexual dimorphism in cortical bone morphology during adolescent growth in Chinese
ba0006p009
Transient hyperphosphatasemia in a child with nephrolithiasis And history of severe prematurity
ba0006p010
Neonatal hypocalcemia - transient neonatal pseudohypoparathyroidism
ba0006p011
Determinants of bone outcomes in adolescent athletes at baseline: The PRO-BONE study
ba0006p012
Longitudinal evaluation of bone mass, geometry and metabolism in adolescent male athletes. The PRO-BONE study
ba0006p013
Longitudinal changes in bone mineral content and bone stiffness in adolescent male athletes: The PRO-BONE study
ba0006p014
Structural geometry of bones is prominently associated with risk of fracture in children
ba0006p015
Necrotizing enterocolitis during the neonatal period is related to lower bone mass at 5 years of age, compared to matched controls
ba0006p016
Bone mineral density in children and adolescents with neurofibromatosis type I: mineralization during growth and pubertal development
ba0006p017
Abstract unavailable
ba0006p018
Zebrafish as model organism for craniosynostosis
ba0006p019
Age at onset of walking affects bone mineral content in early childhood
ba0006p020
Sexual dimorphism in bone size, density, micro-architecture and strength is site-specific and manifested in favour of boys already in childhood
ba0006p021
Bone densitometric parameters and body composition in preterm and term infants at the age of forty weeks of gestational age
ba0006p022
Tracking differences in morphology and regulation between the spine and long bones in a pig model
ba0006p023
Spondyloepiphyseal dysplasia: A rare cause of short stature
ba0006p024
The impact of Haemophilia A on bone health
ba0006p025
Own research experience of bone tissue metabolism in patients with the Ehlers-Danlos syndrome
ba0006p026
Sex and iron modify fibroblast growth factor 23 concentrations in 1-year-old children
ba0006p027
Abstract unavailable
ba0006p028
Web-based surveys using Patient-Reported Outcome Measurement Information System (PROMIS) instruments allow documentation of important components of the disease experience among individuals with Osteogenesis Imperfecta
ba0006p029
Outcomes of zoledronic acid use in paediatric conditions
ba0006p030
Valproic acid induces Fanconi syndrome and reversible hypophosphataemic rickets via upregulation of fibroblast growth factor 23
ba0006p031
Bone health status in Indian children with type 1 diabetes as assessed by peripheral quantitative computer tomography (pQCT)
ba0006p032
Nutritional status influence upon bone mineral density of children with cerebral palsy after reconstructive hip joint surgery
ba0006p033
Identification of bone remodelling alterations in Gorham-Stout disease
ba0006p034
Abstract unavailable
ba0006p035
Decreased incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility
ba0006p036
Early fragility fractures in Zellweger syndrome spectrum - peroxisome dysfunction affecting osteogenesis?
ba0006p037
Hypophosphatasia associated with acute disseminated encephalomyelitis (ADEM): causal relationship or coincidence?
ba0006p038
Cystinosin deficiency affects bone phenotype
ba0006p039
Atypical femoral fractures in 2 children treated with bisphosphonates
ba0006p040
A randomised double-blind placebo-controlled trial of vitamin D supplementation in juvenile-onset systemic lupus erythematosus: positive effect on trabecular microarchitecture using high resolution peripheral quantitative computed tomography
ba0006p041
Osteogenesis imperfecta type VI presenting as suspected physical abuse -- a report of two cases
ba0006p042
Pseudohypoparathyroidism type IB: A cause of late hypocalcemia
ba0006p043
Abstract unavailable
ba0006p044
Abstract unavailable
ba0006p045
A 16 years old follow up in one case of congenital multiple hormone deficiency: growth, sexual development and bone metabolism
ba0006p046
Vitamin D status before and during treatment for childhood cancer
ba0006p047
A rare cause of rickets
ba0006p048
Difficulties in diagnostics and clinical classification of osteogenesis imperfecta in Poland
ba0006p049
The prevalence of fragility fractures in children with cerebral palsy in Greater Manchester, UK-a cross-sectional survey
ba0006p050
Low bone density and fragility fractures in unbalanced translocation T(9;11)
ba0006p051
Hypophosphatasia - from symptom to diagnosis - case report
ba0006p052
Determinants of bone density in Duchenne muscular dystrophy
ba0006p053
The influence of immune dysregulation on bone metabolism in children with inflammatory bowel disease: the potential for bone as a secondary lymphoid organ
ba0006p054
Abstract unavailable
ba0006p055
Conservative management of metabolic derangements in osseous tissue among patients with vitamin d-dependent rickets type 2
ba0006p056
Zebrafish as a model for hypophosphatasia
ba0006p057
The relationship between maternal and child bone density in Nigerian children with and without nutritional rickets
ba0006p058
Retrospective evaluation of serum alkaline phosphatases (ALP) in Italian children referred to a tertiary children's hospital
ba0006p059
Abstract unavailable
ba0006p060
Renal tubular acidosis with an elevated urinary β-2 microglobulin in a boy presenting with sporadic hypophosphataemic rickets and intellectual disability (Dent's Disease)
ba0006p061
Lysinuric protein intolerance presenting with short stature and osteoporosis
ba0006p062
Effects of KRN23, a fully human anti-FGF23 monoclonal antibody, on functional outcomes in children with X-linked hypophosphatemia (XLH): results from a randomized, open-label Phase 2 study
ba0006p063
Extensive periosteal new bone formation secondary to copper deficiency in a 2 year-old boy with arterial tortuosity syndrome
ba0006p064
A novel form of congenital rickets due to a recurrent gain of function mutation in CYP3A4
ba0006p065
Unusual presentation of acquired hypophosphataemic rickets
ba0006p066
Mid-gestation anomaly scan cannot be relied upon for screening for severe perinatal hypophosphatasia
ba0006p067
Craniosynostosis can occur in children with nutritional rickets
ba0006p068
Multiple fractures that begun in utero in a pre-adolescent child with low ALP levels and nephrocalcinosis: clinical aproximation for the differential diagnosis of hypophosphatasia (HPP)
ba0006p069
The abnormally high and heterogeneous bone matrix mineralization after childhood solid organ transplantation is not further increased by bisphosphonate treatment
ba0006p070
In search of hypophosphatasia: a need to establish normative data for low alkaline phosphatase in pediatric population
ba0006p071
Raised intracranial pressure in a boy with Pycnodysostosis with open fontanelles
ba0006p072
Spectrum of paediatric hypophosphataemic rickets in a tertiary centre
ba0006p073
High bone turnover markers and disturbances of bone mineral density in children with hypophosphataemic rickets
ba0006p074
Improvement of bone density in eating disorders correlates with improvements in growth
ba0006p075
Abstract unavailable
ba0006p076
The role of bone age in the evaluation of trabecular bone score (TBS) of children and adolescents 5--19 years old
ba0006p077
Abstract unavailable
ba0006p078
Assessment of a semi-automated software program for the identification of vertebral fractures in children
ba0006p079
Bone age assessment using Greulich and Pyle and Tanner-Whitehouse methods: a systematic review
ba0006p080
Bone age determination using dual-energy X-ray absorptiometry
ba0006p081
Impact of age, sex, location of injury, physical activity, vitamin D and calcium intake on the injury outcome of wrist and ankle in children
ba0006p082
Schmorl's node and vitamin D deficiency: cause or coincidence
ba0006p083
Chronological age, height adjusted age and bone age: Which of them correlates better to bone mineral density in kidney-transplant recipient children?
ba0006p084
Cumulative radiation exposure from diagnostic imaging and associated lifetime cancer risk in children with Osteogenesis Imperfecta
ba0006p085
Feasibility and reproducibility using HRpQCTII in children and adolescents
ba0006p086
Cranial synostosis and Chiari 1 malformation in X-linked hypophosphatemic rickets
ba0006p087
Normative data for lateral distal femur bone mineral density in children from 3 to 18 years of age using Lunar Prodigy absorptiometry
ba0006p088
Cross Calibration of GE Lunar DPX Pro and GE Lunar iDXA
ba0006p089
Intra-observer precision of vertebral height measurements using spine X-Rays And DXA in boys with Duchenne Muscular Dystrophy
ba0006p090
Reliability and validity of DXA based images for measurement of height in children
ba0006p091
Bone mineral density and quantitative ultrasound in the longitudinal monitoring of bone status in patient with Neurofibromatosis Type 1
ba0006p092
A boy with spondylo-epiphyseal dysplasia tarda
ba0006p093
Bone health assessment in children with thalassaemia major
ba0006p094
Legg Calve Perthes disease and growth hormone treatment
ba0006p095
Chronic intermittent torticollis in a toddler: a rare case of axis (C2) Ewing sarcoma presentation
ba0006p096
Evaluation of the use of body quantitative computed tomography for the assessment of the tibia in children with Neurofibromatosis 1
ba0006p097
Preliminary precision-error estimates of bone mineral density in children with cerebral palsy
ba0006p098
Bone strength and microarchitectural deficits in children with cystinosis
ba0006p099
Decreased bone turnover in HIV-infected children on antiretroviral therapy
ba0006p100
Establishing the clinical need for a dedicated service for children and adolescents with Osteogenesis Imperfecta in the Republic of Ireland
ba0006p101
Do measures of adiposity and muscle cross-sectionally predict the health of weight-bearing bones in 11--12 year old Australian children?: A population-based study
ba0006p102
Femoral fractures in infants -- comparison of a population-based and an osteogenesis imperfecta-cohort
ba0006p103
Dietary calcium deficiency contributes to the causation of nutritional rickets (NR) in the United Kingdom (UK): data from the British Paediatric Surveillance Unit (BPSU) NR survey
ba0006p104
Low serum alkaline phosphatase is often not recognised by clinicians
ba0006p105
Does growth hormone and estrogens prevent girls with Turner syndrome from increased fracture rates?
ba0006p106
A case of a novel de novo PLS3 deletion, presenting with vertebral fractures and mild dysmorphism
ba0006p107
Genetic transmission of osteogenesis imperfecta type V by a healthy mosaic carrier father
ba0006p108
Microdeletion of 12p11.22-p11.21 resulting in a skeletal dysplasia characterized by significant metaphyseal abnormalities and osteolysis
ba0006p109
Case report: a potentially new skeletal dysplasia with autosomal recessive inheritance
ba0006p110
Vitamin D-dependent rickets type 1 due to a novel mutation in
CYP27B1
ba0006p111
A novel mutation of CYP27B1 in two siblings with vitamin D-dependent rickets type 1A
ba0006p112
A challenging case of hyperphosphatemic tumoral calcinosis
ba0006p113
Rare copy number variants in array-based comparative genomic hybridization in early-onset skeletal fragility
ba0006p114
Expanding the genotype--phenotype correlation of osteogenesis imperfecta with a novel mutation in Col1A2 gene
ba0006p115
Classical
SATB2
-associated syndrome with severe osteoporosis, recurrent bony fractures and tibial bowing
ba0006p116
Uptake of influenza vaccine in UK patients with fibrodysplasia ossificans progressiva
ba0006p117
Genome-wide association study identifies five novel genetic determinants of dental maturation
ba0006p118
Phenotypic spectrum in Weyers acrofacial dysostosis: A case report
ba0006p119
Vitamin D-dependent rickets - a rare form of rickets - diagnostics and therapeutic problem
ba0006p120
Abstract unavailable
ba0006p121
Bisphosphonate treatment initiated in the newborn period - our experience
ba0006p122
Abstract unavailable
ba0006p123
The treatment of Hyperphosphatemic Familial Tumoral Calcinosis
ba0006p124
Identification and characterization of a novel microRNA inhibiting osteoblast functions by suppressing actin polymerization
ba0006p125
A case of severe reaction following the use of Bisphosphonates in a patient with Osteogenesis Imperfecta
ba0006p126
Growth hormone treatment in two short peri-pubertal brothers with X-linked hypophosphatemic rickets
ba0006p127
Growth and clinical outcome in a 16 year-old male with childhood hypophosphatasia after 1 year therapy with asfotase alfa
ba0006p128
The case of severe osteoporosis in patient with recessive dystrophic Epidermolysis Bullosa
ba0006p129
The impact of intravenous bisphosphonate on vertebral morphometry in children with secondary osteoporosis and vertebral fractures
ba0006p130
The treatment of Camurati-Engelmann disease with Losartan: a case report
ba0006p131
Anti-RANKL treatment in a murine model of fibrous dysplasia
ba0006p132
Long term treatment with intravenous pamidronate in two children with severe form of juvenile Paget's disease
ba0006p133
Improvement in spinal involvement with zoledronic acid in pediatric patients with chronic recurrent multifocal osteomyelitis: a case series
ba0006p134
Continuous subcutaneous PTH infusion in autosomal dominant hypocalcaemia
ba0006p135
Preliminary results for a ramping model of pamidronate administration
ba0006p136
Growth, bone and muscle mass are adversely affected in bone marrow transplant recipients: a body composition analysis
ba0006p137
Fibrodysplasia ossificans progressiva: baseline characteristics of 101 subjects participating in a global, longitudinal, natural history study
ba0006p138
Relative impact of muscle strength and muscle mass on bone mineral density in Japanese adolescents: data from the Kitakata Kids Health Study
ba0006p139
Bone mineral accretion is increased during winter and is positively related to lean mass accretion in healthy children 2--8 years
ba0006p140
Unique correlation pattern between cortical trabecular bone qualities and standard dynamometer handgrip strength in girls with adolescent idiopathic scoliosis (AIS)?
ba0006p141
Walking within 12 months of age is related to higher whole body lean mass and bone mineral density in children at 3 years of age
ba0006p142
Gender differences in bone health in a cohort of adolescents with developmental coordination disorder
ba0006p143
Soft tissues, areal bone mineral density and hip geometry estimates in active young boys: the PRO-BONE study
ba0006p144
Longitudinal growth and bone development in glucocorticoid treated boys with Duchenne muscular dystrophy
ba0006p145
Stature and longitudinal growth in glucocorticoid naive boys with Duchenne Muscular Dystrophy
ba0006p146
Bone health in boys with Duchenne muscular dystrophy (DMD): the dichotomy between bone density and fracture
ba0006p147
Muscle density measurement in muscular dystrophy
ba0006p148
Abstract unavailable
ba0006p149
DXA based evaluation of the bone mass and body composition in a group of Romanian cystic fibrosis children
ba0006p150
Characterisation of skeletal developmental in mouse models of Duchenne Muscular Dystrophy
ba0006p151
Seasonal variation in internet searches for vitamin D
ba0006p152
Vitamin D intake and status in children 2-18 years: a meta-analysis
ba0006p153
Maximal suppression of parathyroid hormone as a determinant of optimal vitamin D status in adolescents
ba0006p154
Dietary protein is associated with bone adaptations and performance of pre-adolescents
ba0006p155
Bone health status of underprivileged Indian adolescent girls
ba0006p156
Are there gender differences in abdominal fat distribution in healthy teenagers?
ba0006p157
Bone metabolism in adolescent girls with anorexia nervosa
ba0006p158
Maternal calcium supplementation in a rural Gambian population associated with reduced blood pressure among adolescent female, but not male, offspring
ba0006p159
Maternal calcium supplementation in a rural Gambian population associated with reduced height and weight among adolescent female, but not male, offspring
ba0006p160
Early-life vitamin D status and bone mass at five years in a prospective birth cohort study
ba0006p161
Nutritional rickets presenting to secondary care in children (<16 years) -- A UK surveillance study
ba0006p162
Vitamin D insufficiency and inadequate bone mineral status in newcomer immigrant and refugee children in Canada
ba0006p163
Abstract unavailable
ba0006p164
Abstract unavailable
ba0006p165
Abstract unavailable
ba0006p166
Stable and functional osteosynthesis with intramedullary growing rods: results of surgical correction in eleven patients with systemic skeletal disease
ba0006p167
Cortico-cancellous bone allografting in treatment of children with orthopedic diseases
ba0006p168
Orthopaedic management of leg length discrepancy in Proteus syndrome: a case series
ba0006p169
Physical activity is negatively correlated with circulating sclerostin in 6--12 year-old children
ba0006p170
Review of lower limb range of movement following intramedullary fixation in children with Osteogensis Imperfecta
ba0006p171
Bone health at 11-12 years, physical activity and sedentariness: a cross-sectional Australian population-based study
ba0006p172
Results of surgical treatment of tibia deformity in patients with Campanaccis disease
ba0006p173
Maffucci syndrome - as an extremely rare form of Ollier disease
ba0006p174
Management of Gorham disease in the cervicothoracic spine with mobile gravity traction and Sirolimus
ba0006p175
System epidermal nevus with hyperkeratosis and violations of bone tissue metabolism -- therapy of drug of pamidrinic acid and surgical orthopedic treatment. Case from practice
ba0006p176
The elbow in type V osteogenesis imperfecta: is early functional loss related to radiographic findings?
ba0006p177
Abstract unavailable
ba0006p178
Skeletal health of young patients with perinatal HIV infection: Experience from a reference center
ba0006p179
Abstract unavailable
ba0006p180
Generalized arterial calcinosis of infancy: a case of a new mutation with central nervous system involvement and good response to bisphosphonates
ba0006p181
Osteonecrosis results in significant long term morbidity in patients with acute lymphoblastic leukaemia
ba0006p182
The treatment of severe pain in melorheostosis with daily walking program only: a case report
ba0006p183
Physical activity and health-related quality of life in patients with chronic non-bacterial osteomyelitis - pilot and model project in a rare inflammatory bone disease
ba0006p184
Effects of vitamin D with calcium supplementation or zinc supplementation on the incidence of infections in school children: a randomized controlled trial
ba0006p185
Is cherubism a systemic disease? Prospective study about 9 patients
ba0006p186
Acroosteolysis presenting as nail resorption
ba0006p187
Paradoxical response of serum parathyroid hormone concentration in response to vitamin D and calcium supplementation in undernourished Indian children
ba0006p188
A deep phenotyping of autosomal dominant osteopetrosis type 2 (ADO2) mouse model revealed multiorgan dysfunctions
ba0006p189
Development of an
in vitro
model of cancer stem cells from a rare human telangiectatic osteosarcoma
ba0006p190
Juvenile hypophosphatasia presenting with short stature: a case report
ba0006p191
Development of an osteogenesis imperfecta specific quality of life measure
ba0006p192
Sheffield children's hospital osteogenesis imperfecta service: collaboration and care
ba0006p193
Variable learning disability and behavioural difficulties in children with familial hypocalciuric hypercalcaemia type 3
ba0006p194
Concentrated growth factor for the treatment of intrabony defects in chronic periodontitis in adolescents
ba0006p195
A qualitative enquiry examining the lived experience of mothers who have children with osteogenesis imperfecta
ba0006p196
Financial burden in families of children with osteogenesis imperfecta (OI)
ba0006p197
Hearing the patient's voice: a focus group listening to the child and parent experiences of living with rare bone diseases
ba0006p198
Validation of questionnaire for measurement of sunlight exposure in children from Pune, India
ba0006p199
The platform of expertise for rare diseases Paris-Sud: an innovative model for gathering reference centers and improving care for rare diseases
ba0006p200
Posture cushions impact on spinal alignment in children with osteogenesis imperfecta - true or false?
ba0006p201
Osteosarcoma-derived Extracellular Vesicles induce tumoral-like phenotypes in normal cells
ba0006p202
Neurofibromatosis type 1 (NF1) associated congenital pseudarthrosis of the Tibia and Fibula misdiagnosed as non-accidental injury (NAI)
ba0006p203
Is a modified version of the Childhood Health Assessment Questionnaire (CHAQ) a useful tool to identify the level of disability in children with osteogenesis imperfecta?
ba0006p204
Osteopathologies and endocrine late effects in a cohort of 102 juvenile survivors of brain tumors
ba0006p205
Lysinuric protein intolerance associated with vertebral fractures and IGF-I deficiency
ba0006p206
Bone turnover in the obese children is related to gender, body compo-sition and leptin level
ba0006p207
Social barriers and needs of children with osteogenesis imperfecta (OI): a qualitative descriptive interview-based study
ba0006p208
Intensive therapy - a week of multi-disciplinary intervention at Sheffield Children's Hospital: An example of goal setting and positive outcomes
ba0006p209
Late Breaking Oral Communication Abstracts
(1)
Treatment with a Novel activin receptor IIB ligand trap improves muscle mass and bone geometry in a mouse model of severe Osteogenesis Imperfecta
ba0006lb1
The regulation of Smpd3 expression in skeletal tissues and its role in fracture healing
ba0006lb2
Mediating effect of muscle on the relationship of physical activity trajectories and bone outcomes: The Iowa Bone Development Study
ba0006lb3
Serious adverse effects of denosumab in adolescents treated for giant cell tumour of the bone: osteonecrosis of the jaw and rebound hypercalcaemia with acute kidney injury
ba0006lb4
Role of type III sodium/phosphate co-transporters in the responsiveness of osteoblasts to extracellular inorganic phosphate
ba0006lb5
Altered bone metabolism in Fanconi anemia results from defective mesenchymal stem cell differentiation
ba0006lb6
Musculoskeletal system in adolescents with type 1 diabetes
ba0006lb7
Breech presentation is associated with neonatal and early childhood deficits in bone mass and size
ba0006lb8
The cellular immune response in children with inflammatory bowel disease may mediate their low bone mineral density: a pilot study
ba0006lb9
Effects of long-term sedentary behaviour on the cortical bone mass and distribution during growth: The HAPPY bone study
ba0006lb10
Bone health status as measured by DXA and pQCT in Indian Children with Thalassemia Major
ba0006lb11
Correlation of the first fracture time and COL1A1/2 mutations in patients with Osteogenesis Imperfecta
ba0006lb12
Low dose of intravenous pamidronate therapy in quadriplegic children with osteoporosis
ba0006lb13
P4HB recurrent missense mutation causing Cole-Carpenter syndrome: exploring the underlying mechanism
ba0006lb14
Consensus paper - Physiotherapy in children with OI
ba0006lb15
Implementing an osteoporosis disease management program: what works and what doesn't work
ba0006lb16
Bone health among boys with duchenne muscular dystrophy after initiation of glucocorticoids
ba0006lb17
Occurrence of vitamin D and vitamin K deficiency in children with low-energy fractures
ba0006lb18
Selected risk factors of fractures in children -own observation
ba0006lb19
COL2A1 c.1609G[gt]A (p.Gly537Ser) a pathogenic variant causing multiple skeletal abnormalities and severe short stature
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Morbid obesity and respiratory failure in a child with pseudohypoparathyroidism type 1A
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