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Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review.
Jurca, Claudia Maria; Iuhas, Oana; Kozma, Kinga; Petchesi, Codruta Diana; Zaha, Dana Carmen; Bembea, Marius; Jurca, Sanziana; Paul, Corina; Jurca, Alexandru Daniel.
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  • Jurca CM; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
  • Iuhas O; Regional Center of Medical Genetics Bihor, County Emergency Clinical Hospital Oradea, Romania, (Part of ERN THACA), 410469 Oradea, Romania.
  • Kozma K; Regional Center of Medical Genetics Bihor, County Emergency Clinical Hospital Oradea, Romania, (Part of ERN THACA), 410469 Oradea, Romania.
  • Petchesi CD; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
  • Zaha DC; Regional Center of Medical Genetics Bihor, County Emergency Clinical Hospital Oradea, Romania, (Part of ERN THACA), 410469 Oradea, Romania.
  • Bembea M; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
  • Jurca S; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
  • Paul C; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
  • Jurca AD; Faculty of Medicine and Pharmacy, Department of Preclinical Disciplines, 1 December Sq., University of Oradea, 410081 Oradea, Romania.
Genes (Basel) ; 13(8)2022 08 04.
Article en En | MEDLINE | ID: mdl-36011303
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar / Genu Varum Tipo de estudio: Guideline Límite: Child / Female / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía Pais de publicación: Suiza
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Raquitismo Hipofosfatémico Familiar / Genu Varum Tipo de estudio: Guideline Límite: Child / Female / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía Pais de publicación: Suiza