547 related articles for article (PubMed ID: 19944211)
1. 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]
2. Genetic prevalence and characteristics in children with recurrent pancreatitis.
Sultan M; Werlin S; Venkatasubramani N
J Pediatr Gastroenterol Nutr; 2012 May; 54(5):645-50. PubMed ID: 22094894
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
Tzetis M; Kaliakatsos M; Fotoulaki M; Papatheodorou A; Doudounakis S; Tsezou A; Makrythanasis P; Kanavakis E; Nousia-Arvanitakis S
Clin Genet; 2007 May; 71(5):451-7. PubMed ID: 17489851
[TBL] [Abstract][Full Text] [Related]
9. Hereditary chronic pancreatitis.
Teich N; Mössner J
Best Pract Res Clin Gastroenterol; 2008; 22(1):115-30. PubMed ID: 18206817
[TBL] [Abstract][Full Text] [Related]
10. Analysis of CFTR, SPINK1, PRSS1 and AAT mutations in children with acute or chronic pancreatitis.
Sobczyńska-Tomaszewska A; Bak D; Oralewska B; Oracz G; Norek A; Czerska K; Mazurczak T; Teisseyre M; Socha J; Zagulski M; Bal J
J Pediatr Gastroenterol Nutr; 2006 Sep; 43(3):299-306. PubMed ID: 16954950
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hereditary chronic pancreatitis.
Rosendahl J; Bödeker H; Mössner J; Teich N
Orphanet J Rare Dis; 2007 Jan; 2():1. PubMed ID: 17204147
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Clinical and morphological characteristics of sporadic genetically determined pancreatitis as compared to idiopathic pancreatitis: higher risk of pancreatic cancer in CFTR variants.
Hamoir C; Pepermans X; Piessevaux H; Jouret-Mourin A; Weynand B; Habyalimana JB; Leal T; Geubel A; Gigot JF; Deprez PH
Digestion; 2013; 87(4):229-39. PubMed ID: 23751316
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Genetic counseling for hereditary pancreatitis--the role of molecular genetics testing for the cationic trypsinogen gene, cystic fibrosis and serine protease inhibitor Kazal type 1.
Ellis I
Gastroenterol Clin North Am; 2004 Dec; 33(4):839-54. PubMed ID: 15528021
[TBL] [Abstract][Full Text] [Related]
18. Association of SPINK1 gene mutation and CFTR gene polymorphisms in patients with pancreas divisum presenting with idiopathic pancreatitis.
Garg PK; Khajuria R; Kabra M; Shastri SS
J Clin Gastroenterol; 2009 Oct; 43(9):848-52. PubMed ID: 19593166
[TBL] [Abstract][Full Text] [Related]
19. High incidence of PRSS1 and SPINK1 mutations in Korean children with acute recurrent and chronic pancreatitis.
Lee YJ; Kim KM; Choi JH; Lee BH; Kim GH; Yoo HW
J Pediatr Gastroenterol Nutr; 2011 Apr; 52(4):478-81. PubMed ID: 21415673
[TBL] [Abstract][Full Text] [Related]
20. CFTR, SPINK1, PRSS1, and CTRC mutations are not associated with pancreatic cancer in German patients.
Schubert S; Traub F; Brakensiek K; von Kopylow K; Marohn B; Maelzer M; Gaedcke J; Kreipe H; Stuhrmann M
Pancreas; 2014 Oct; 43(7):1078-82. PubMed ID: 25003218
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
