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Intra-individual biological variation in sweat chloride concentrations in CF, CFTR dysfunction, and healthy pediatric subjects.
Cirilli, Natalia; Raia, Valeria; Rocco, Ilaria; De Gregorio, Fabiola; Tosco, Antonella; Salvadori, Laura; Sepe, Angela Ornella; Buzzetti, Roberto; Minicuci, Nadia; Castaldo, Giuseppe.
Afiliação
  • Cirilli N; Mother-Child Department, Cystic Fibrosis Referral Care Center, United Hospitals, Ancona, Italy.
  • Raia V; Regional Cystic Fibrosis Care Unit, Department of Translational Medical Sciences, University "Federico II", Naples, Italy.
  • Rocco I; Neuroscience Institute, CNR, Padova, Italy.
  • De Gregorio F; Regional Cystic Fibrosis Care Unit, Department of Translational Medical Sciences, University "Federico II", Naples, Italy.
  • Tosco A; Regional Cystic Fibrosis Care Unit, Department of Translational Medical Sciences, University "Federico II", Naples, Italy.
  • Salvadori L; Regional Cystic Fibrosis Care Unit, Department of Translational Medical Sciences, University "Federico II", Naples, Italy.
  • Sepe AO; Regional Cystic Fibrosis Care Unit, Department of Translational Medical Sciences, University "Federico II", Naples, Italy.
  • Buzzetti R; Epidemiologist, Bergamo, Italy.
  • Minicuci N; Neuroscience Institute, CNR, Padova, Italy.
  • Castaldo G; CEINGE-Biotecnologie Avanzate, Naples, Italy.
Pediatr Pulmonol ; 53(6): 728-734, 2018 06.
Article em En | MEDLINE | ID: mdl-29611353
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Suor / Cloretos / Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Suor / Cloretos / Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article