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Administration and monitoring of clofazimine for NTM infections in children with and without cystic fibrosis.
Cameron, L H; Peloquin, C A; Hiatt, P; Mann, M; Starke, J R; Faircloth, J; McNeil, J C; Patel, A; Ruiz, F.
Afiliación
  • Cameron LH; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Infectious Diseases, United States. Electronic address: lindsay.cameron@bcm.edu.
  • Peloquin CA; University of Florida, Department of Pharmacy, United States.
  • Hiatt P; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Pulmonology, United States.
  • Mann M; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Pulmonology, United States.
  • Starke JR; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Infectious Diseases, United States.
  • Faircloth J; Section of Pediatric Pulmonology, United States; Texas Children's Hospital, Department of Pharmacy, United States.
  • McNeil JC; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Infectious Diseases, United States.
  • Patel A; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Pulmonology, United States.
  • Ruiz F; Baylor College of Medicine, Department of Pediatrics, United States; Section of Pediatric Pulmonology, United States.
J Cyst Fibros ; 21(2): 348-352, 2022 03.
Article en En | MEDLINE | ID: mdl-34479810

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Quística / Infecciones por Mycobacterium no Tuberculosas Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Humans Idioma: En Revista: J Cyst Fibros Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Quística / Infecciones por Mycobacterium no Tuberculosas Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Humans Idioma: En Revista: J Cyst Fibros Año: 2022 Tipo del documento: Article