Editorial: The ESPGHAN cystic fibrosis working group: Defining dios and constipation in cystic fibrosis with a multicenter study on the incidence, characteristics, and treatment of DIOS

Journal of Pediatric Gastroenterology and Nutrition

Volumn 50, Issue 1, 2010, Pages 8-

  Raia, V ^a   Fuiano, L ^a   Staiano, A ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; CONSTIPATION; CYSTIC FIBROSIS; DISTAL INTESTINAL OBSTRUCTION SYNDROME; EDITORIAL; GENE MUTATION; HUMAN; INTESTINE OBSTRUCTION; LIFE EXPECTANCY; MECONIUM ILEUS; PRIORITY JOURNAL; GENETICS; GENOTYPE; ILEUM DISEASE; MECONIUM; MULTICENTER STUDY; MUTATION; NOTE;

CONSTIPATION; CYSTIC FIBROSIS; GENOTYPE; HUMANS; ILEAL DISEASES; INTESTINAL OBSTRUCTION; MECONIUM; MULTICENTER STUDIES AS TOPIC; MUTATION;

EID: 76149102247     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e3181a6da59     Document Type: Editorial

References (4)

1. Houwen RHJ, van der Doef HPJ, Sermet I, et al. The ESPGHAN Cystic Fibrosis Working Group: Defining DIOS and Constipation in Cystic Fibrosis with a multicenter study on the incidence, characteristics and treatment of DIOS. J Pediatr Gastroenterol Nutr 2009;49:X-X.
2. Ratjen F, Doring G. Cystic fibrosis. Lancet 2003;361:681-689
3. Chaudry G, Navarro OM, Levine DS, et al. Abdominal manifestations of cystic fibrosis in children. Pediatr Radiol 2006;36:233-240
4. Borowitz D, Durie PR, Clarke LL, Werlin SL, et al. Gastrointestinal outcomes and confounders in cystic fibrosis. J Pediatr Gastroenterol Nutr 2005;41:273-285