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Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries.
Magner, Martin; Almássy, Zsuzsanna; Gucev, Zoran; Kiec-Wilk, Beata; Plaiasu, Vasilica; Tylki-Szymanska, Anna; Zafeiriou, Dimitrios; Zaganas, Ioannis; Lampe, Christina.
Afiliação
  • Magner M; Department of Paediatrics and Inherited Metabolic Disorders, General University Hospital and First Faculty of Medicine, Charles University, KPDPM 1. LF UK a VFN v Praze, Ke Karlovu 2, 128 08, Prague, Czech Republic. martin.magner@vfn.cz.
  • Almássy Z; Department of Toxicology and Metabolic Diseases, Heim Pal National Pediatric Institute, Budapest, Hungary.
  • Gucev Z; University Children's Hospital, Skopje, North Macedonia.
  • Kiec-Wilk B; Unit of Rare Metabolic Diseases, Department of Metabolic Diseases, Jagiellonian University Medical College, University Hospital, Krakow, Poland.
  • Plaiasu V; Regional Centre of Medical Genetics, INSMC Alessandrescu-Rusescu, Bucharest, Romania.
  • Tylki-Szymanska A; Department of Pediatric Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland.
  • Zafeiriou D; First Department of Pediatrics, Hippokratio General Hospital, Aristotle University, Thessaloniki, Greece.
  • Zaganas I; Neurogenetics Laboratory, Neurology Department, University Hospital of Heraklion, University of Crete, Heraklion, Greece.
  • Lampe C; Department of Child Neurology, Epileptology and Social Pediatrics, Centre for Rare Diseases, University of Giessen, Giessen, Germany.
Orphanet J Rare Dis ; 17(1): 190, 2022 05 10.
Article em En | MEDLINE | ID: mdl-35538504
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mucopolissacaridoses / Mucopolissacaridose IV Tipo de estudo: Guideline / Qualitative_research Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: República Tcheca País de publicação: Reino Unido
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mucopolissacaridoses / Mucopolissacaridose IV Tipo de estudo: Guideline / Qualitative_research Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: República Tcheca País de publicação: Reino Unido