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24. [Release of pancreatic polypeptide after administration of cholecystokinin in children with mucoviscidosis]. Cichy W; Socha J; Barra E Pediatr Pol; 1985 Jun; 60(6):440-4. PubMed ID: 4069838 [No Abstract] [Full Text] [Related]
25. Studies of the function of the sweat gland, parotid gland and the pancreas in chronic bronchitis and heterozygous mucoviscidosis or cystic fibrosis. Toivonen S Ann Med Intern Fenn; 1967; 56(50):Suppl 50:9-48. PubMed ID: 6050826 [No Abstract] [Full Text] [Related]
26. The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). Kerem E; Corey M; Kerem BS; Rommens J; Markiewicz D; Levison H; Tsui LC; Durie P N Engl J Med; 1990 Nov; 323(22):1517-22. PubMed ID: 2233932 [TBL] [Abstract][Full Text] [Related]
27. Relationship between bile acid malabsorption and pancreatic insufficiency in cystic fibrosis. Weber AM; Roy CC; Chartrand L; Lepage G; Dufour OL; Morin CL; Lasalle R Gut; 1976 Apr; 17(4):295-9. PubMed ID: 773791 [TBL] [Abstract][Full Text] [Related]
29. [Changes in the pancreatic and respiratory functions in cystic fibrosis. The influence of the time of the evolution of the disease]. Ericson N; Navarro S; Valderrama R; Adrián MJ; Lloberes P; Cobos N Med Clin (Barc); 1993 Nov; 101(17):650-2. PubMed ID: 8289509 [TBL] [Abstract][Full Text] [Related]
30. Refining the continuum of CFTR-associated disorders in the era of newborn screening. Levy H; Nugent M; Schneck K; Stachiw-Hietpas D; Laxova A; Lakser O; Rock M; Dahmer MK; Biller J; Nasr SZ; Baker M; McColley SA; Simpson P; Farrell PM Clin Genet; 2016 May; 89(5):539-49. PubMed ID: 26671754 [TBL] [Abstract][Full Text] [Related]
31. Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D. Parad RB J Med Genet; 1996 Aug; 33(8):711-3. PubMed ID: 8863168 [TBL] [Abstract][Full Text] [Related]
32. [Diagnosis and treatment of exocrine pancreatic insufficiency in mucoviscidosis]. Shmerling DH Z Allgemeinmed; 1972 Aug; 48(24):1080-4. PubMed ID: 4649650 [No Abstract] [Full Text] [Related]
33. [Exocrine pancreatic function in infants with cystic fibrosis]. Hager-Malecka B; Janiec W; Lukas W; Kalaciński W; Bielecka W Pol Tyg Lek; 1977 Mar; 32(13):485-7. PubMed ID: 850652 [No Abstract] [Full Text] [Related]
34. [Cystic fibrosis: analysis of 24 cases]. Kimura HM; Rozov T; Barbieri D; Nakaie CM; Cardieri JM Rev Paul Med; 1982; 99(1):13-7. PubMed ID: 7146739 [No Abstract] [Full Text] [Related]
35. The steatocrit: a simple method for monitoring fat malabsorption in patients with cystic fibrosis. Colombo C; Maiavacca R; Ronchi M; Consalvo E; Amoretti M; Giunta A J Pediatr Gastroenterol Nutr; 1987; 6(6):926-30. PubMed ID: 3681578 [TBL] [Abstract][Full Text] [Related]
36. Complex cystic fibrosis allele R334W-R1158X results in reduced levels of correctly processed mRNA in a pancreatic sufficient patient. Duarte A; Amaral M; Barreto C; Pacheco P; Lavinha J Hum Mutat; 1996; 8(2):134-9. PubMed ID: 8844211 [TBL] [Abstract][Full Text] [Related]
38. Pathophysiological aspects of pancreatic diseases in childhood. The case of cystic fibrosis. Mastella G; Baldessari G; Olivieri D; Pederzini F; Rizzotti P; Zanchetta M; Burlina A Ric Clin Lab; 1984; 14(3):367-81. PubMed ID: 6522957 [No Abstract] [Full Text] [Related]
39. Stool elastase as a diagnostic test for pancreatic function in children with cystic fibrosis. Wallis C; Leung T; Cubitt D; Reynolds A Lancet; 1997 Oct; 350(9083):1001. PubMed ID: 9329517 [No Abstract] [Full Text] [Related]
40. Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndrome. Ren CL; Desai H; Platt M; Dixon M Pediatr Pulmonol; 2011 Nov; 46(11):1079-84. PubMed ID: 21538969 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]