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Detection of iron deficiency in children with Down syndrome.
Hart, Sarah J; Zimmerman, Kanecia; Linardic, Corinne M; Cannon, Sheila; Pastore, Anna; Patsiogiannis, Vasiliki; Rossi, Paolo; Santoro, Stephanie L; Skotko, Brian G; Torres, Amy; Valentini, Diletta; Vellody, Kishore; Worley, Gordon; Kishnani, Priya S.
Affiliation
  • Hart SJ; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA. sarah.hart@duke.edu.
  • Zimmerman K; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Linardic CM; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Cannon S; Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
  • Pastore A; Down Syndrome Center of Western Pennsylvania, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Patsiogiannis V; Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Rossi P; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
  • Santoro SL; Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Skotko BG; Department of Pediatrics, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Torres A; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
  • Valentini D; Division of Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
  • Vellody K; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Worley G; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
  • Kishnani PS; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Genet Med ; 22(2): 317-325, 2020 02.
Article de En | MEDLINE | ID: mdl-31417190
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome de Down / Anémie par carence en fer / Ferritines Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limites: Child / Child, preschool / Female / Humans / Infant / Male Langue: En Journal: Genet Med Sujet du journal: GENETICA MEDICA Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome de Down / Anémie par carence en fer / Ferritines Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limites: Child / Child, preschool / Female / Humans / Infant / Male Langue: En Journal: Genet Med Sujet du journal: GENETICA MEDICA Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique