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Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype.
Barber, Andrew T; Shapiro, Adam J; Davis, Stephanie D; Ferkol, Thomas W; Atkinson, Jeffrey J; Sagel, Scott D; Dell, Sharon D; Olivier, Kenneth N; Milla, Carlos E; Rosenfeld, Margaret; Li, Lang; Lin, Feng-Chang; Sullivan, Kelli M; Capps, Nicole A; Zariwala, Maimoona A; Knowles, Michael R; Leigh, Margaret W.
Afiliación
  • Barber AT; Department of Pediatrics, UNC Children's, and.
  • Shapiro AJ; Department of Pediatrics, McGill University Health Centre Research Institute, Montreal, Quebec, Canada.
  • Davis SD; Department of Pediatrics, UNC Children's, and.
  • Ferkol TW; Department of Pediatrics and.
  • Atkinson JJ; Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
  • Sagel SD; Department of Pediatrics, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado.
  • Dell SD; Department of Pediatrics, BC Children's Hospital, Vancouver, British Columbia, Canada.
  • Olivier KN; Pulmonary Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland.
  • Milla CE; Department of Pediatrics, Stanford University, Palo Alto, California.
  • Rosenfeld M; Department of Pediatrics, Seattle Children's Hospital, University of Washington School of Medicine, Seattle, Washington; and.
  • Li L; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Lin FC; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Sullivan KM; Department of Medicine.
  • Capps NA; Marsico Lung Institute.
  • Zariwala MA; Department of Medicine.
  • Knowles MR; Marsico Lung Institute.
  • Leigh MW; Marsico Lung Institute.
Ann Am Thorac Soc ; 20(3): 397-405, 2023 03.
Article en En | MEDLINE | ID: mdl-36342963

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Kartagener / Trastornos de la Motilidad Ciliar / Síndrome de Heterotaxia Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Ann Am Thorac Soc Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Kartagener / Trastornos de la Motilidad Ciliar / Síndrome de Heterotaxia Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Ann Am Thorac Soc Año: 2023 Tipo del documento: Article