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XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH).
Seefried, Lothar; Alzahrani, Ali; Arango Sancho, Pedro; Bacchetta, Justine; Crowley, Rachel; Emma, Francesco; Gibbins, Jonathan; Grandone, Anna; Javaid, Muhammad Kassim; Mindler, Gabriel; Raimann, Adalbert; Rothenbuhler, Anya; Tucker, Ian; Zeitlin, Leonid; Linglart, Agnès.
Afiliação
  • Seefried L; Orthopedic Institute, König-Ludwig Haus, University of Würzburg, Würzburg, Germany.
  • Alzahrani A; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Arango Sancho P; Department of Pediatric Nephrology, Hospital Sant Joan de Déu, Barcelona, Spain.
  • Bacchetta J; Department of Onco-Nephrology, Pediatric Cancer Center, Barcelona, Spain.
  • Crowley R; Pediatric Nephrology, Reference Center for Rare Diseases of Calcium and Phosphate, Filières OSCAR et ORKID, INSERM1033, Hospices Civils de Lyon, Lyon, France.
  • Emma F; St Vincent's University Hospital and Rare Disease Clinical Trial Network, University College Dublin, Dublin, Ireland.
  • Gibbins J; Division of Nephrology, Children's Hospital Bambino Gesù-IRCCS, Rome, Italy.
  • Grandone A; Evelina London Children's Hospital, London, UK.
  • Javaid MK; Department of Woman, Child, General and Specialized Surgery, University of Campania L. Vanvitelli, Naples, Italy.
  • Mindler G; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
  • Raimann A; Department of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Vienna, Austria.
  • Rothenbuhler A; Vienna Bone and Growth Center, Vienna, Austria.
  • Tucker I; Vienna Bone and Growth Center, Vienna, Austria.
  • Zeitlin L; APHP, Endocrinology and Diabetology for Children, Bicêtre Paris Saclay Hospital, Le Kremlin-Bicêtre, France.
  • Linglart A; APHP, Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Filière OSCAR, Paris, France.
Orphanet J Rare Dis ; 18(Suppl 2): 333, 2023 Oct 27.
Article em En | MEDLINE | ID: mdl-37885021
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Raquitismo Hipofosfatêmico Familiar Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Raquitismo Hipofosfatêmico Familiar Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article