Measurement of fecal elastase improves performance of newborn screening for cystic fibrosis

Journal of Cystic Fibrosis

Volumn 15, Issue 3, 2016, Pages 313-317

  Barben, Juerg ^a   Rueegg, Corina S ^b,c   Jurca, Maja ^b   Spalinger, Johannes ^d   Kuehni, Claudia E ^b   Barazzone, Constance ^e   Baumgartner, Matthias ^e   Casaulta, Carmen ^e   Eng, Peter ^e   Fingerhut, Ralph ^e   Gallati, Sabina ^e   Hafen, Gaudenz ^e   Hammer, Juerg ^e   Jung, Andreas ^e   Moeller, Alex ^e   Mornand, Anne ^e   Mueller, Dominik ^e   Regamey, Nicolas ^e   Rochat, Isabelle ^e   Schiller, Barbara ^e   Schoeni, Martin H ^e   Spinas, Renate ^e   Torresani, Toni ^e   Trachsel, Daniel ^e   Zanolari, Maura ^e   more..

^a Kantonsspital St Gallen   (Switzerland)

^b UNIVERSITY OF BERN   (Switzerland)

^c UNIVERSITY OF LUCERNE   (Switzerland)

^d LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^e NONE   (Switzerland)

Author keywords

CFSPID; Cystic fibrosis; Fecal elastase; Newborn screening

Indexed keywords

DNA; ELASTASE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; PANCREATIC ELASTASE; TRYPSINOGEN;

ARTICLE; CYSTIC FIBROSIS; DNA DETERMINATION; DNA SCREENING; FECES ANALYSIS; FECES LEVEL; HUMAN; NEWBORN; NEWBORN SCREENING; PANCREAS; PRACTICE GUIDELINE; PROGNOSIS; SWEAT TEST; SWITZERLAND; ALGORITHM; CLASSIFICATION; CLINICAL PROTOCOL; EARLY DIAGNOSIS; EARLY INTERVENTION; EPIDEMIOLOGY; GENETIC SCREENING; GENETICS; METABOLISM; PROCEDURES; STANDARDS; SWEAT; TIME FACTOR; TOTAL QUALITY MANAGEMENT;

ALGORITHMS; CLINICAL PROTOCOLS; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EARLY DIAGNOSIS; EARLY MEDICAL INTERVENTION; GENETIC TESTING; HUMANS; INFANT, NEWBORN; NEONATAL SCREENING; PANCREATIC ELASTASE; PROGNOSIS; QUALITY IMPROVEMENT; SWEAT; SWITZERLAND; TIME FACTORS; TRYPSINOGEN;

EID: 84955573754     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2015.12.024     Document Type: Article

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