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Correction: Characterizing the neurological phenotype of the hyperinsulinism hyperammonemia syndrome.
Rosenfeld, Elizabeth; Nanga, Ravi Prakash Reddy; Lucas, Alfredo; Revell, Andrew Y; Thomas, Allison; Thomas, Nina H; Roalf, David R; Shinohara, Russell T; Reddy, Ravinder; Davis, Kathryn A; De León, Diva D.
Afiliación
  • Rosenfeld E; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, 3500 Civic Center Boulevard, Philadelphia, PA, 19140, USA. rosenfelde@chop.edu.
  • Nanga RPR; Congenital Hyperinsulinism Center, Children's Hospital of Philadelphia, Philadelphia, PA, USA. rosenfelde@chop.edu.
  • Lucas A; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. rosenfelde@chop.edu.
  • Revell AY; Center for Advanced Metabolic Imaging in Precision Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
  • Thomas A; Penn Center for Neuroengineering and Therapeutics, University of Pennsylvania, Philadelphia, PA, USA.
  • Thomas NH; Penn Center for Neuroengineering and Therapeutics, University of Pennsylvania, Philadelphia, PA, USA.
  • Roalf DR; Behavioral Neuroscience Core, Center for Human Phenomic Science, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Shinohara RT; Behavioral Neuroscience Core, Center for Human Phenomic Science, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Reddy R; Department of Child and Adolescent Psychiatry and Behavioral Sciences, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Davis KA; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
  • De León DD; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Orphanet J Rare Dis ; 17(1): 315, 2022 Aug 18.
Article en En | MEDLINE | ID: mdl-35982497
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos