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Journal Abstract Search

193 related items for PubMed ID: 12658038

  • 1. Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 test.
    Walkowiak J, Nousia-Arvanitakis S, Agguridaki C, Fotoulaki M, Strzykala K, Balassopoulou A, Witt M, Herzig KH.
    J Pediatr Gastroenterol Nutr; 2003 Apr; 36(4):474-8. PubMed ID: 12658038
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  • 3. Fecal elastase-1 is superior to fecal chymotrypsin in the assessment of pancreatic involvement in cystic fibrosis.
    Walkowiak J, Herzig KH, Strzykala K, Przyslawski J, Krawczynski M.
    Pediatrics; 2002 Jul; 110(1 Pt 1):e7. PubMed ID: 12093988
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  • 5. Serum lipase after secretin stimulation detects mild pancreatic involvement in cystic fibrosis.
    Walkowiak J, Nousia-Arvanitakis S, Lisowska A, Piotrowski R, Strzykala K, Bychowiec B, Songin T, Galli-Tsinopoulou A, Sands D, Pidonia I, Krawczynski M, Milanowski A, Herzig KH.
    J Pediatr Gastroenterol Nutr; 2004 Apr; 38(4):430-5. PubMed ID: 15085023
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  • 7. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K, Weren M, Proesmans M, Kerem E.
    Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
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  • 8. Exocrine pancreatic function testing in patients with cystic fibrosis and pancreatic sufficiency: a correlation study.
    Weintraub A, Blau H, Mussaffi H, Picard E, Bentur L, Kerem E, Stankiewicz H, Wilschanski M.
    J Pediatr Gastroenterol Nutr; 2009 Mar; 48(3):306-10. PubMed ID: 19274786
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  • 11. Faecal elastase-1 and fat-soluble vitamin profiles in patients with cystic fibrosis in Western Norway.
    Dorlöchter L, Aksnes L, Fluge G.
    Eur J Nutr; 2002 Aug; 41(4):148-52. PubMed ID: 12242582
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  • 12. The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype.
    Augarten A, Ben Tov A, Madgar I, Barak A, Akons H, Laufer J, Efrati O, Aviram M, Bentur L, Blau H, Paret G, Wilschanski M, Kerem BS, Yahav Y.
    Eur J Gastroenterol Hepatol; 2008 Mar; 20(3):164-8. PubMed ID: 18301294
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  • 13. Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency.
    Walkowiak J, Herzig KH, Witt M, Pogorzelski A, Piotrowski R, Barra E, Sobczynska-Tomaszewska A, Trawinska-Bartnicka M, Strzykala K, Cichy W, Sands D, Rutkiewicz E, Krawczynski M.
    Eur J Clin Invest; 2001 Sep; 31(9):796-801. PubMed ID: 11589722
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  • 14. Fecal elastase-1 is decreased in villous atrophy regardless of the underlying disease.
    Walkowiak J, Herzig KH.
    Eur J Clin Invest; 2001 May; 31(5):425-30. PubMed ID: 11380594
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  • 16. Faecal elastase-1 concentration in cystic fibrosis patients with CFTR I1234V mutation.
    Abdel Rahman H, Abdul Wahab A, Abdel Rahman MO, Mostafa OA.
    Acta Paediatr; 2006 Sep; 95(9):1066-9. PubMed ID: 16938751
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  • 17. Diagnostic accuracy of fecal elastase 1 assay in patients with pancreatic maldigestion or intestinal malabsorption: a collaborative study of the Italian Society of Pediatric Gastroenterology and Hepatology.
    Carroccio A, Verghi F, Santini B, Lucidi V, Iacono G, Cavataio F, Soresi M, Ansaldi N, Castro M, Montalto G.
    Dig Dis Sci; 2001 Jun; 46(6):1335-42. PubMed ID: 11414313
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  • 18. Fecal chymotrypsin and elastase-1 determination on one single stool collected at random: diagnostic value for exocrine pancreatic status.
    Molinari I, Souare K, Lamireau T, Fayon M, Lemieux C, Cassaigne A, Montaudon D.
    Clin Biochem; 2004 Sep; 37(9):758-63. PubMed ID: 15329313
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  • 20. Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosis.
    Borowitz D, Baker SS, Duffy L, Baker RD, Fitzpatrick L, Gyamfi J, Jarembek K.
    J Pediatr; 2004 Sep; 145(3):322-6. PubMed ID: 15343184
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