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Persistent Lung Disease in Adults with NKX2.1 Mutation and Familial Neuroendocrine Cell Hyperplasia of Infancy.
Nevel, Rebekah J; Garnett, Errine T; Worrell, John A; Morton, Ronald L; Nogee, Lawrence M; Blackwell, Timothy S; Young, Lisa R.
Afiliación
  • Nevel RJ; 1 Division of Pulmonary Medicine, Department of Pediatrics.
  • Garnett ET; 2 Division of Allergy, Pulmonary, and Critical Care, Department of Medicine, and.
  • Worrell JA; 3 Department of Radiology and Radiological Sciences, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Morton RL; 4 Division of Pulmonary Medicine, University of Louisville, Louisville, Kentucky; and.
  • Nogee LM; 5 Eudowood Neonatal Pulmonary Division, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland.
  • Blackwell TS; 2 Division of Allergy, Pulmonary, and Critical Care, Department of Medicine, and.
  • Young LR; 1 Division of Pulmonary Medicine, Department of Pediatrics.
Ann Am Thorac Soc ; 13(8): 1299-304, 2016 08.
Article en En | MEDLINE | ID: mdl-27187870
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Células Neuroendocrinas / Factor Nuclear Tiroideo 1 / Pulmón Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ann Am Thorac Soc Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Células Neuroendocrinas / Factor Nuclear Tiroideo 1 / Pulmón Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ann Am Thorac Soc Año: 2016 Tipo del documento: Article