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Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.
Aalbers, Bente L; Yaakov, Yasmin; Derichs, Nico; Simmonds, Nicholas J; De Wachter, Elke; Melotti, Paola; De Boeck, Kris; Leal, Teresinha; Tümmler, Burkhart; Wilschanski, Michael; Bronsveld, Inez.
Afiliación
  • Aalbers BL; Department of Pulmonology, University Medical Center Utrecht, Postbus 85500, 3508, GA, Utrecht, the Netherlands. Electronic address: b.l.aalbers-2@umcutrecht.nl.
  • Yaakov Y; Pediatric Gastroenterology Unit and Cystic Fibrosis Center, Hadassah-Hebrew University Medical Center, Kiryat Hadassah, POB 12000, Jerusalem 91120, Israel.
  • Derichs N; CF Center, Pediatric Pulmonology and Immunology, Charité Universitätsmedizin, Charitépl. 1, 10117 Berlin, Germany.
  • Simmonds NJ; Department of Cystic Fibrosis, Royal Brompton Hospital and Imperial College, Sydney Street, SW3 6NP London, United Kingdom.
  • De Wachter E; Department of Pediatric Pneumology, UZ Brussel, Laarbeeklaan 101, B-1090 Brussels, Belgium.
  • Melotti P; Cystic Fibrosis Centre, Azienda Ospedaliera Universitaria Integrata. Piazzale Aristide Stefani 1, 37126 Verona, Italy.
  • De Boeck K; Department of Pediatric Pulmonology, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium.
  • Leal T; Louvain Centre for Toxicology and Applied Pharmacology (LTAP), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain, Place de l'Université 1, B-1348 Louvain-la-Neuve, Brussels, Belgium.
  • Tümmler B; CF Center and Clinical Research Group, Department of Pediatric Pneumology and Neonatology, OE 6710, Medical School Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
  • Wilschanski M; Pediatric Gastroenterology Unit and Cystic Fibrosis Center, Hadassah-Hebrew University Medical Center, Kiryat Hadassah, POB 12000, Jerusalem 91120, Israel.
  • Bronsveld I; Department of Pulmonology, University Medical Center Utrecht, Postbus 85500, 3508, GA, Utrecht, the Netherlands.
J Cyst Fibros ; 19(4): 627-631, 2020 07.
Article en En | MEDLINE | ID: mdl-31331863
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sudor / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística / Potenciales de la Membrana / Mucosa Nasal Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sudor / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística / Potenciales de la Membrana / Mucosa Nasal Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Año: 2020 Tipo del documento: Article