Newborn screening for cystic fibrosis: Science, legislation, and human values

By Pollitt R. J.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 8, 2003-01 ,pp. : 725-727

Springer Publishing Company

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Neonatal screening for cystic fibrosis: France rises to the challenge

By Farriaux J. P.   Vidailhet M.   Briard M. L.   Belot V.   Dhondt J. L.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 8, 2003-01 ,pp. : 729-744

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The influence of sex, gestational age, birth weight, blood transfusion, and timing of the heel prick on the pancreatitis-associated protein concentration in newborn screening for cystic fibrosis

By Vernooij-van Langen Annette   Loeber J.   Elvers Bert   Triepels Ralf   Roefs Jos   Gille Johan   Reijntjens Sandra   Dompeling Edward   Dankert-Roelse Jeannette  

Journal of Inherited Metabolic Disease, Vol. 36, Iss. 1, 2013-01 ,pp. : 147-154

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Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European population

By Sommerburg Olaf   Lindner Martin   Muckenthaler Martina   Kohlmueller Dirk   Leible Svenja   Feneberg Reinhard   Kulozik Andreas   Mall Marcus   Hoffmann Georg  

Journal of Inherited Metabolic Disease, Vol. 33, Iss. 2, 2010-10 ,pp. : 263-271

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Newborn urine screening programme in the province of Quebec: An update of 30 years' experience

By Auray-Blais C.   Giguére R.   Lemieux B.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 4, 2003-06 ,pp. : 393-402

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