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Newborn Screening for Vitamin B6 Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy.
Okun, Jürgen G; Gan-Schreier, Hongying; Ben-Omran, Tawfeq; Schmidt, Kathrin V; Fang-Hoffmann, Junmin; Gramer, Gwendolyn; Abdoh, Ghassan; Shahbeck, Noora; Al Rifai, Hilal; Al Khal, Abdul Latif; Haege, Gisela; Chiang, Chuan-Chi; Kasper, David C; Wilcken, Bridget; Burgard, Peter; Hoffmann, Georg F.
Afiliação
  • Okun JG; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany. juergen.okun@med.uni-heidelberg.de.
  • Gan-Schreier H; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Ben-Omran T; Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
  • Schmidt KV; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Fang-Hoffmann J; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Gramer G; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Abdoh G; Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
  • Shahbeck N; Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
  • Al Rifai H; Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
  • Al Khal AL; Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
  • Haege G; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Chiang CC; Chinese Foundation of Health, Taipei City, Taiwan.
  • Kasper DC; Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
  • Wilcken B; NSW Newborn Screening Programme, The Children's Hospital at Westmead, Westmead, NSW, Australia.
  • Burgard P; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
  • Hoffmann GF; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
JIMD Rep ; 32: 87-94, 2017.
Article em En | MEDLINE | ID: mdl-27325427
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: JIMD Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: JIMD Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos