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International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up.
Welling, Lindsey; Bernstein, Laurie E; Berry, Gerard T; Burlina, Alberto B; Eyskens, François; Gautschi, Matthias; Grünewald, Stephanie; Gubbels, Cynthia S; Knerr, Ina; Labrune, Philippe; van der Lee, Johanna H; MacDonald, Anita; Murphy, Elaine; Portnoi, Pat A; Õunap, Katrin; Potter, Nancy L; Rubio-Gozalbo, M Estela; Spencer, Jessica B; Timmers, Inge; Treacy, Eileen P; Van Calcar, Sandra C; Waisbren, Susan E; Bosch, Annet M.
Afiliação
  • Welling L; Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
  • Bernstein LE; Section of Clinical Genetics and Metabolism, Inherited Metabolic Disease Nutrition Department, University of Colorado-Denver School of Medicine, The Children's Hospital Colorado, Aurora, CO, USA.
  • Berry GT; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Burlina AB; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Eyskens F; Department of Pediatrics, Metabolic Unit, University Hospital, University of Padova, Padova, Italy.
  • Gautschi M; Department of Metabolic Disorders in Children, Antwerp University Hospital UZA, Edegem, Belgium.
  • Grünewald S; University Children's Hospital, Pediatric Endocrinology, Diabetes and Metabolism, and Institute of Clinical Chemistry, Inselspital, University of Bern, Bern, Switzerland.
  • Gubbels CS; Metabolic Unit, Great Ormond Street Hospital and Institute of Child Health, University College London, London, UK.
  • Knerr I; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Labrune P; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • van der Lee JH; National Centre for Inherited Metabolic Disorders, Temple St. Children's University Hospital, Dublin, Ireland.
  • MacDonald A; Department of Pediatrics, APHP, Hopital Antoine Béclère, Cedex Clamart, France.
  • Murphy E; Pediatric Clinical Research Office, Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
  • Portnoi PA; Birmingham Children's Hospital, Steelhouse Lane, Birmingham, UK.
  • Õunap K; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
  • Potter NL; Medical Advisory Panel, Galactosemia Support Group UK, West Midlands, UK.
  • Rubio-Gozalbo ME; Department of Pediatrics, University of Tartu, Tartu, Estonia.
  • Spencer JB; Department of Genetics, Tartu University Hospital, Tartu, Estonia.
  • Timmers I; Department of Speech and Hearing Sciences, Washington State University, Spokane, WA, USA.
  • Treacy EP; Department of Pediatrics and Laboratory Genetic Metabolic Diseases, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Van Calcar SC; Department of Gynecology and Obstetrics, School of Medicine, Emory University, Atlanta, Georgia.
  • Waisbren SE; Department of Cognitive Neuroscience, Maastricht University, Maastricht, The Netherlands.
  • Bosch AM; National Centre for Inherited Metabolic Disorders, Temple St. Children's University Hospital and Mater Misericordiae University Hospital, Dublin, Ireland.
J Inherit Metab Dis ; 40(2): 171-176, 2017 03.
Article em En | MEDLINE | ID: mdl-27858262
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Galactosemias Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Galactosemias Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article