122 related articles for article (PubMed ID: 28176071)
1. 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]
2. 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]
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. Cystic fibrosis gene mutations detected in hereditary pancreatitis.
Ravnik-Glavac M; Glavac D; di Sant' Agnese P; Chernick M; Dean M
Pflugers Arch; 1996; 431(6 Suppl 2):R191-2. PubMed ID: 8992448
[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. 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]
7. [Hereditary pancreatitis].
Kim YT
Korean J Gastroenterol; 2005 Feb; 45(2):143-7. PubMed ID: 15725720
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Trypsinogen gene mutations in patients with chronic or recurrent acute pancreatitis.
Truninger K; Köck J; Wirth HP; Muellhaupt B; Arnold C; von Weizsäcker F; Seifert B; Ammann RW; Blum HE
Pancreas; 2001 Jan; 22(1):18-23. PubMed ID: 11138965
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis.
Nishimori I; Kamakura M; Fujikawa-Adachi K; Morita M; Onishi S; Yokoyama K; Makino I; Ishida H; Yamamoto M; Watanabe S; Ogawa M
Gut; 1999 Feb; 44(2):259-63. PubMed ID: 9895387
[TBL] [Abstract][Full Text] [Related]
14. 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]
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. 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]
17. 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]
18. Identification of a hereditary pancreatitis mutation in four West Virginia families.
Elitsur Y; Chertow BC; Jewell RD; Finver SN; Primerano DA
Pediatr Res; 1998 Dec; 44(6):927-30. PubMed ID: 9853929
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Screening for mutations of the cationic trypsinogen gene: are they of relevance in chronic alcoholic pancreatitis?
Teich N; Mössner J; Keim V
Gut; 1999 Mar; 44(3):413-6. PubMed ID: 10026330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
