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Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis.
Abdul Majeed, Nehna; Font-Montgomery, Esperanza; Lukose, Linda; Bryant, Joy; Veppumthara, Peter; Choyke, Peter L; Turkbey, Ismail B; Heller, Theo; Gahl, William A; Gunay-Aygun, Meral.
Afiliación
  • Abdul Majeed N; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA; MedStar Health, Internal Medicine, Baltimore, MD, USA.
  • Font-Montgomery E; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA; University of Missouri, Department of Pediatrics and Medical Genetics, Columbia, MO 65212, USA.
  • Lukose L; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA; RBK Pediatrics, Commack, NY 11725, USA.
  • Bryant J; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Veppumthara P; Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
  • Choyke PL; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Turkbey IB; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Heller T; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Gahl WA; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, MD 20892, USA.
  • Gunay-Aygun M; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA; Johns Hopkins University School of Medicine, McKusick-Nathans Department of Genetic Medicine, Department of Pediatrics, Baltimore, MD 2128
Mol Genet Metab ; 131(1-2): 267-276, 2020.
Article en En | MEDLINE | ID: mdl-32919899
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Riñón Poliquístico Autosómico Recesivo / Receptores de Superficie Celular / Enfermedades Genéticas Congénitas / Hipertensión Portal / Cirrosis Hepática Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Riñón Poliquístico Autosómico Recesivo / Receptores de Superficie Celular / Enfermedades Genéticas Congénitas / Hipertensión Portal / Cirrosis Hepática Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article