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57th Annual ESPE

Athens, Greece
27 Sep 2018 - 29 Sep 2018

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ESPE 2018 57th European Society for Paediatric Endocrinology Annual Meeting 27-29 September 2018 Athens, Greece

Rapid Free Communications

Bone, Growth Plate & Mineral Metabolism 1

High-Resolution MRI Imaging of Bone-Muscle-Fat in Glucocorticoid Treated Boys with Duchenne Muscular Dystrophy: Results from the ScOT-DMD Study
aDevelopmental Endocrinology Research Group, Royal Hospital for Children, Glasgow, UK; bPaediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, UK; cClinical Physics, NHS Greater Glasgow & Clyde, Glasgow, UK; dScottish Muscle Network, West of Scotland Genetic Services, Queen Elizabeth University Hospital, Glasgow, UK
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S-25OHD is Associated with Hand Grip Strength and Myopathy at Five Years in Girls: An Odense Child Cohort Study
aUniversity of Southern Denmark, Odense, Denmark; bOdense University Hospital, Odense, Denmark; cMental Health Services in the Region of Southern Denmark, Odense, Denmark; dHans Christian Andersen’s Hospital, Odense University Hospital, Odense, Denmark
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Measured Free 25-Hydroxyvitamin D in Healthy Children and Relationship to Total 25-Hydroxyvitamin D, Calculated Free 25-Hydroxyvitamin D and Vitamin D Binding Protein
aPaediatrics Department, Germans Trias i Pujol University Hospital, Badalon, Badalona, Spain; bClinical Biochemistry Department, Germans Trias i Pujol University Hospital, Badalona, Spain; cGermans Trias i Pujol University Hospital, Badalona, Spain.
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Novel Severe Skeletal Dysplasia with Under-Mineralisation Associated with Reduced In Utero Calcium Transport and TRPV6 Compound Heterozygous Variants
aDepartment of Paediatric Endocrinology, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Foundation Trust, Bristol, UK; bInstitute of Biomedical and Clinical Science, University of Exeter, Exeter, UK; cDepartment of Molecular Genetics, Royal Devon and Exeter Hospital, Exeter, UK; dDepartment of Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, UK; eDepartment of Fetomaternal Medicine, Derriford Hospital, Plymouth, UK; fDepartment of Paediatric Respiratory Medicine, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Foundation Trust, Bristol, UK; gDepartment of Clinical Genetics, St Michaels Hospital, University Hospitals Bristol NHS Foundation Trust, Bristol, UK; hBristol Medical School, Translational Health Sciences, University of Bristol, Bristol, UK
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Identification of Characteristic Neurological Complications in Infants with Achondroplasia by Routine MRI Screening
aGuy’s and St Thomas’ NHS Foundation Trust, London, UK; bGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK
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The Novel R211Q POP1 Homozygous Mutation Causes Severe Short Stature But Uniquely Only Subtle Skeletal Dysplasia
aPalestine Red Crescent Society Hospital, Hebron, Palestine; bBethlehem Arab Society for Rehabilitation, Beit Jala, Palestine; cShare Zedek Medical Center, Jerusalem, Israel; dHadassah Hebrew University Medical Center, Jerusalem, Israel
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