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Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.
Haffner, Dieter; Emma, Francesco; Eastwood, Deborah M; Duplan, Martin Biosse; Bacchetta, Justine; Schnabel, Dirk; Wicart, Philippe; Bockenhauer, Detlef; Santos, Fernando; Levtchenko, Elena; Harvengt, Pol; Kirchhoff, Martha; Di Rocco, Federico; Chaussain, Catherine; Brandi, Maria Louisa; Savendahl, Lars; Briot, Karine; Kamenicky, Peter; Rejnmark, Lars; Linglart, Agnès.
Afiliación
  • Haffner D; Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hannover, Germany. Haffner.Dieter@mh-hannover.de.
  • Emma F; Center for Congenital Kidney Diseases, Center for Rare Diseases, Hannover Medical School, Hannover, Germany. Haffner.Dieter@mh-hannover.de.
  • Eastwood DM; Department of Pediatric Subspecialties, Division of Nephrology, Children's Hospital Bambino Gesù - IRCCS, Rome, Italy.
  • Duplan MB; Department of Orthopaedics, Great Ormond St Hospital for Children, Orthopaedics, London, UK.
  • Bacchetta J; The Catterall Unit Royal National Orthopaedic Hospital NHS Trust, Stanmore, UK.
  • Schnabel D; Dental School, Université Paris Descartes Sorbonne Paris Cité, Montrouge, France.
  • Wicart P; APHP, Department of Odontology, Bretonneau Hospital, Paris, France.
  • Bockenhauer D; APHP, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, and Filière OSCAR, Paris, France.
  • Santos F; Department of Pediatric Nephrology, Rheumatology and Dermatology, University Children's Hospital, Lyon, France.
  • Levtchenko E; Center for Chronic Sick Children, Pediatric Endocrinology, Charitè, University Medicine, Berlin, Germany.
  • Harvengt P; APHP, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, and Filière OSCAR, Paris, France.
  • Kirchhoff M; APHP, Department of Pediatric Orthopedic Surgery, Necker - Enfants Malades University Hospital, Paris, France.
  • Di Rocco F; Paris Descartes University, Paris, France.
  • Chaussain C; University College London, Centre for Nephrology and Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Brandi ML; Hospital Universitario Central de Asturias (HUCA), University of Oviedo, Oviedo, Spain.
  • Savendahl L; Department of Pediatric Nephrology and Development and Regeneration, University Hospitals Leuven, University of Leuven, Leuven, Belgium.
  • Briot K; RVRH-XLH, French Patient Association for XLH, Suresnes, France.
  • Kamenicky P; Phosphatdiabetes e.V., German Patient Association for XLH, Lippstadt, Germany.
  • Rejnmark L; Pediatric Neurosurgery, Hôpital Femme Mère Enfant, Centre de Référence Craniosténoses, Université de Lyon, Lyon, France.
  • Linglart A; Dental School, Université Paris Descartes Sorbonne Paris Cité, Montrouge, France.
Nat Rev Nephrol ; 15(7): 435-455, 2019 07.
Article en En | MEDLINE | ID: mdl-31068690
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Nat Rev Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Nat Rev Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania