58th Annual ESPE meeting
Vienna,
Austria
19 Sep 2019 - 21 Sep 2019
The theme of this year’s meeting is Variety and Variation in Paediatric Endocrinology. Join us in Vienna to explore the diversity we encounter in our discipline and the care that we have to exercise when using the term “normality”. Whilst gaining an update on the latest treatments, clinical best practice and cutting edge research in the field of paediatric endocrinology.
Free Communications
Bone, Growth Plate and Mineral Metabolism Session 1
Continued Improvement in Clinical Outcomes with Burosumab, a Fully Human Anti-FGF23 Monoclonal Antibody: Results from a 3-Year, Phase 2, Clinical Trial in Children with X-Linked Hypophosphatemia (XLH)
Linglart Agnès
Carpenter Thomas O.
Högler Wolfgang
Imel Erik A.
Portale Anthony A.
Boot Annemieke
Padidela Raja
Van't Hoff William
Mao Meng
Skrinar Alison
Scott Roberts Mary
San Martin Javier
Whyte Michael P.
1APHP Hôpital Bicêtre Paris Sud, New Haven, France. 2Yale School of Medicine, New Haven, USA. 3Johannes Kepler University Linz, Linz, Austria. 4Indiana University School of Medicine, Indianapolis, USA. 5University of California, San Francisco, San Francisco, USA. 6University of Groningen, Groningen, Netherlands. 7Royal Manchester Children's Hospital, Manchester, United Kingdom. 8Great Ormond Street Hospital, London, United Kingdom. 9Ultragenyx Pharmaceutical Inc, Novato, USA. 10Shriners Hospital for Children and Washington University School of Medicine, St. Louis, USA
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Benefits of Long-Term Burosumab Persist in 11 Girls with X-Linked Hypophosphatemia (XLH) Who Transitioned into Adolescence During the Phase 2 CL201 Trial
Boot Annemieke
Carpenter Thomas O.
Högler Wolfgang
Imel Erik A.
Portale Anthony A.
Linglart Agnès
Padidela Raja
Van't Hoff William
Mao Meng
Skrinar Alison
Scott Roberts Mary
San Martin Javier
Whyte Michael P.
1University of Groningen, New Haven, Netherlands. 2Yale School of Medicine, New Haven, USA. 3Johannes Kepler University Linz, Linz, Austria. 4Indiana University School of Medicine, Indianapolis, USA. 5University of California, San Francisco, San Francisco, USA. 6APHP Hôpital Bicêtre Paris Sud, Le Kremlin-Bicêtre, France. 7Royal Manchester Children's Hospital, Manchester, United Kingdom. 8Great Ormond Street Hospital, London, United Kingdom. 9Ultragenyx Pharmaceutical Inc, Novato, USA. 10Shriners Hospital for Children and Washington University School of Medicine, St. Louis, USA
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Higher Dose of Burosumab is Needed for Treatment of Children with Severe Forms of X-Linked Hypophosphatemia
Zhukouskaya Volha
Audrain Christelle
Lambert Anne-Sophie
Kamenicky Peter
Adamsbaum Catherine
Nevoux Jerome
Chaussain Catherine
Wicart Philippe
Briot Karine
Di Rocco Federico
Colao Annamaria
Di Somma Carolina
Trabado Séverine
Prié Dominique
Rothenbuhler Anya
Linglart Agnès
1APHP, Reference Center for Rare Disorders of the Calcium and Phosphate Metabolism, Filiere OSCAR and Platform of expertise for rare diseases Paris-Sud, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 2Department of Clinical Medicine and Surgery, Division of Endocrinology, University of Naples Federico II, Naples, Italy. 3APHP, Department of Endocrinology and Diabetology for children, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 4APHP, Department of Endocrinology and Reproductive Diseases, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 5Paris Sud – Paris Saclay University, Faculté de Médecine, Le Kremlin-Bicetre, France. 6APHP, Department Pediatric Radiology, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 7APHP, Department of ORL, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 8APHP, Department of Odontology-Maladies Rares, Hospital Bretonneau Paris, Paris, France. 9Université Paris Descartes Paris, Paris, France. 10APHP, Department of Pediatric orthopaedic surgery, Necker - Sick Kids University Hospital, Paris, France. 11APHP, Department of Rheumatology Hospital Cochin, Paris, France. 12Pediatric Neurosurgery, Hospital Femme Mere Enfant, Hospices Civiles de Lyon and University Claude Bernard Lyon, Bron Cedex, France. 13Reference Center for Craniosynostosis, INSERM 1033, Lyon, France. 14APHP, Department of Molecular Genetics, Pharmacogenetics and Hormonology, Bicêtre Paris-Sud Hospital, Le Kremlin-Bicetre, France. 15APHP, Hôpital Necker Enfants Malades,15APHP, Hôpital Necker Enfants Malades, INSERM U115115APHP, Hôpital Necker Enfants Malades, INSERM U1151 INSERM U1151, Paris, France
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New Imaging Approaches to the Quantification of Musculoskeletal Alterations in X-linked Hypophosphatemic Rickets (XLH)
Raimann Adalbert
Mehany Sarah N.
Feil Patricia
Weber Michael
Pietschmann Peter
Boni-Mikats Andrea
Klepochova Radka
Krssak Martin
Haeusler Gabriele
Schneider Johannes
Raum Kay
Patsch Janina
1Medical University of Vienna, Vienna, Austria. 2The High Field MR Centre, Vienna, Austria. 3Charité - Universitätsmedizin Berlin, Berlin, Germany. 4Medical University of Vienna, Vienna, Germany
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Age and Gender-Specific Reference Data for High-Resolution Magnetic Resonance Based Musculoskeletal Parameters in Healthy Children and Young People
Elsharkasi Huda M.
Chen ¹Suet C.
Steell Lewis
Joseph Shuko
Abdalrahman Naiemh
Johnston Blair
Foster John E.
Wong Sze C.
Ahmed S. Faisal
1Developmental Endocrinology Research Group, School of Medicine, Dentistry & Nursing, University of Glasgow, Royal Hospital for Children, Glasgow, United Kingdom. 2Department of Clinical Physics and Bioengineering, NHS Greater Glasgow & Clyde and University of Glasgow, Glasgow, United Kingdom
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Validation of a New Version of BoneXpert Bone Age in Children with Congenital Adrenal Hyperplasia (CAH), Precocious Puberty (PP), Growth Hormone Deficiency (GHD), Turner Syndrome (TS), and other Short Stature Diagnoses
1Visiana, Hørsholm, Denmark. 2University Children's Hospital, Tübingen, Germany. 3Witten/Herdecke University, Herdecke, Germany
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ESPE Abstracts
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