Neonates with cystic fibrosis have a reduced nasal liquid pH; A small pilot study

Journal of Cystic Fibrosis

Volumn 13, Issue 4, 2014, Pages 373-377

  Abou Alaiwa, Mahmoud H ^a   Beer, Alison M ^a   Pezzulo, Alejandro A ^a   Launspach, Janice L ^a   Horan, Rebecca A ^a   Stoltz, David A ^a   Starner, Timothy D ^a   Welsh, Michael J ^a   Zabner, Joseph ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

Airway surface liquid (ASL); Cystic fibrosis; Neonatal screen; Neonates; PH

Indexed keywords

ACIDITY; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; HUMAN; MALE; NASAL AIRWAY SURFACE LIQUID PH; NEWBORN; NEWBORN DISEASE; NEWBORN MONITORING; NEWBORN SCREENING; NORMAL VALUE; PEDIATRICS; PH; PH MEASUREMENT; PILOT STUDY; RESPIRATORY TRACT PARAMETERS; ADOLESCENT; BODY FLUID; CHEMISTRY; FOLLOW UP; GENETICS; GENOTYPE; INFANT; METABOLISM; MIDDLE AGED; MUTATION; NOSE MUCOSA; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SECRETION (PROCESS); YOUNG ADULT;

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADOLESCENT; ADULT; BODY FLUIDS; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; HUMANS; HYDROGEN-ION CONCENTRATION; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGED; MUTATION; NASAL MUCOSA; PILOT PROJECTS; RETROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84902333159     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2013.12.006     Document Type: Article

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