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A retrospective study of adult patients with noncirrhotic hyperammonemia.
Stergachis, Andrew B; Mogensen, Kris M; Khoury, Charbel C; Lin, Alexander P; Peake, Roy Wa; Baker, Joshua J; Barkoudah, Ebrahim; Sahai, Inderneel; Sweetser, David A; Berry, Gerard T; Krier, Joel B.
Afiliación
  • Stergachis AB; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Mogensen KM; Department of Nutrition, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Khoury CC; Renal Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Lin AP; Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Peake RW; Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Baker JJ; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Barkoudah E; Hospital Medicine Unit, Division of General Internal Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Sahai I; Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Sweetser DA; Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Berry GT; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Krier JB; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Inherit Metab Dis ; 43(6): 1165-1172, 2020 11.
Article en En | MEDLINE | ID: mdl-32713002
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hiperamonemia / Trastornos Innatos del Ciclo de la Urea Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Inherit Metab Dis Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hiperamonemia / Trastornos Innatos del Ciclo de la Urea Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Inherit Metab Dis Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos