Is clinical status at diagnosis a prognostic factor in CF infants identified by neonatal screening?
Author:
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference19 articles.
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1. Question 2 Quelle stratégie pour maintenir un état nutritionnel optimal? Quelle strategie pour maintenir un état nutritionnel optimal chez les patients atteints de mucoviscidose? Quand et comment évaluer l'état nutritionnel et les moyens d'iinterventions thérapeutiques?;Archives de Pédiatrie;2003-08
2. CFTR gene: molecular analysis in patients from South Brazil;Molecular Genetics and Metabolism;2003-04
3. Évaluation du diagnostic et du suivi de la cohorte normande d'enfants dépistés atteints de mucoviscidose;Archives de Pédiatrie;2001-08
4. Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis;American Journal of Medical Genetics;1998-04-01
5. Failure to thrive: the earliest feature of cystic fibrosis in infants diagnosed by neonatal screening;Acta Paediatrica;1997-11
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