186 related articles for article (PubMed ID: 10653140)
1. Evidence that hereditary pancreatitis is genetically heterogeneous disorder.
Ravnik-Glavac M; Dean M; di Sant'Agnese P; Chernick M; Kozelj M; Krizman I; Glavac D
Pflugers Arch; 2000; 439(3 Suppl):R50-2. PubMed ID: 10653140
[TBL] [Abstract][Full Text] [Related]
2. Evidence that hereditary pancreatitis is genetically heterogeneous disorder.
Ravnik-Glavač M; Dean M; Sant'Agnese PD; Chernick M; Koželj M; Križman I; Glavač D
Pflugers Arch; 2000 Jan; 439(Suppl 1):r050-r052. PubMed ID: 28176071
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of hereditary pancreatitis.
Chen JM; Ferec C
Eur J Hum Genet; 2000 Jul; 8(7):473-9. PubMed ID: 10909845
[TBL] [Abstract][Full Text] [Related]
4. Heterogeneity in hereditary pancreatitis.
Dasouki MJ; Cogan J; Summar ML; Neblitt W; Foroud T; Koller D; Phillips JA
Am J Med Genet; 1998 Apr; 77(1):47-53. PubMed ID: 9557894
[TBL] [Abstract][Full Text] [Related]
5. Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis.
Ockenga J; Stuhrmann M; Ballmann M; Teich N; Keim V; Dörk T; Manns MP
Am J Gastroenterol; 2000 Aug; 95(8):2061-7. PubMed ID: 10950058
[TBL] [Abstract][Full Text] [Related]
6. Genetic aspects of chronic pancreatitis.
Teich N; Mössner J
Med Sci Monit; 2004 Dec; 10(12):RA325-8. PubMed ID: 15567996
[TBL] [Abstract][Full Text] [Related]
7. Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis.
Creighton JE; Lyall R; Wilson DI; Curtis A; Charnley RM
Br J Surg; 2000 Feb; 87(2):170-5. PubMed ID: 10671922
[TBL] [Abstract][Full Text] [Related]
8. Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
Teich N; Bauer N; Mössner J; Keim V
Am J Gastroenterol; 2002 Feb; 97(2):341-6. PubMed ID: 11866271
[TBL] [Abstract][Full Text] [Related]
9. CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in Brazilian patients.
Bernardino AL; Guarita DR; Mott CB; Pedroso MR; Machado MC; Laudanna AA; Tani CM; Almeida FL; Zatz M
JOP; 2003 Sep; 4(5):169-77. PubMed ID: 14526128
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
Férec C; Raguénès O; Salomon R; Roche C; Bernard JP; Guillot M; Quéré I; Faure C; Mercier B; Audrézet MP; Guillausseau PJ; Dupont C; Munnich A; Bignon JD; Le Bodic L
J Med Genet; 1999 Mar; 36(3):228-32. PubMed ID: 10204851
[TBL] [Abstract][Full Text] [Related]
11. The variable phenotype of the p.A16V mutation of cationic trypsinogen (PRSS1) in pancreatitis families.
Grocock CJ; Rebours V; Delhaye MN; Andrén-Sandberg A; Weiss FU; Mountford R; Harcus MJ; Niemczyck E; Vitone LJ; Dodd S; Jørgensen MT; Ammann RW; Schaffalitzky de Muckadell O; Butler JV; Burgess P; Kerr B; Charnley R; Sutton R; Raraty MG; Devière J; Whitcomb DC; Neoptolemos JP; Lévy P; Lerch MM; Greenhalf W;
Gut; 2010 Mar; 59(3):357-63. PubMed ID: 19951905
[TBL] [Abstract][Full Text] [Related]
12. Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.
Weiss FU; Simon P; Bogdanova N; Mayerle J; Dworniczak B; Horst J; Lerch MM
Gut; 2005 Oct; 54(10):1456-60. PubMed ID: 15987793
[TBL] [Abstract][Full Text] [Related]
13. Genetic, epidemiological, and clinical aspects of hereditary pancreatitis: a population-based cohort study in Denmark.
Joergensen MT; Brusgaard K; Crüger DG; Gerdes AM; Schaffalitzky de Muckadell OB
Am J Gastroenterol; 2010 Aug; 105(8):1876-83. PubMed ID: 20502448
[TBL] [Abstract][Full Text] [Related]
14. Novel mutation and polymorphism of PRSS1 gene in the Chinese patients with hereditary pancreatitis and chronic pancreatitis.
Liu QC; Gao F; Ou QS; Zhuang ZH; Lin SR; Yang B; Cheng ZJ
Chin Med J (Engl); 2008 Jan; 121(2):108-11. PubMed ID: 18272034
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the cationic trypsinogen (PRSS1) gene, and the serine protease inhibitor, Kazal type 1 (SPINK1) gene in patients with alcoholic chronic pancreatitis.
Perri F; Piepoli A; Stanziale P; Merla A; Zelante L; Andriulli A
Eur J Hum Genet; 2003 Sep; 11(9):687-92. PubMed ID: 12939655
[TBL] [Abstract][Full Text] [Related]
16. Determination of the relative contribution of three genes-the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene-to the etiology of idiopathic chronic pancreatitis.
Audrézet MP; Chen JM; Le Maréchal C; Ruszniewski P; Robaszkiewicz M; Raguénès O; Quéré I; Scotet V; Férec C
Eur J Hum Genet; 2002 Feb; 10(2):100-6. PubMed ID: 11938439
[TBL] [Abstract][Full Text] [Related]
17. Identification of CFTR, PRSS1, and SPINK1 mutations in 381 patients with pancreatitis.
Keiles S; Kammesheidt A
Pancreas; 2006 Oct; 33(3):221-7. PubMed ID: 17003641
[TBL] [Abstract][Full Text] [Related]
18. Screening for human cationic trypsinogen (PRSS1) and trypsinogen inhibitor gene (SPINK1) mutations in a Finnish family with hereditary pancreatitis.
Räty S; Piironen A; Babu M; Pelli H; Sand J; Uotila S; Nordback I; Herzig KH
Scand J Gastroenterol; 2007 Aug; 42(8):1000-5. PubMed ID: 17613931
[TBL] [Abstract][Full Text] [Related]
19. Hereditary pancreatitis in children: surgical implications with special regard to genetic background.
Schmitt F; Le Henaff G; Piloquet H; Leclair MD; David A; Heloury Y; Podevin G
J Pediatr Surg; 2009 Nov; 44(11):2078-82. PubMed ID: 19944211
[TBL] [Abstract][Full Text] [Related]
20. Pancreatitis risk in primary hyperparathyroidism: relation to mutations in the SPINK1 trypsin inhibitor (N34S) and the cystic fibrosis gene.
Felderbauer P; Karakas E; Fendrich V; Bulut K; Horn T; Lebert R; Holland-Letz T; Schmitz F; Bartsch D; Schmidt WE
Am J Gastroenterol; 2008 Feb; 103(2):368-74. PubMed ID: 18076731
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
