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Items: 1 to 20 of 540

1.

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.

PMID:
17489851
2.

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.

PMID:
16954950
3.

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.

4.
5.

Identification of CFTR, PRSS1, and SPINK1 mutations in 381 patients with pancreatitis.

Keiles S, Kammesheidt A.

Pancreas. 2006 Oct;33(3):221-7.

PMID:
17003641
6.

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. Epub 2007 Dec 12.

PMID:
18076731
7.

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. Epub 2005 Jun 29.

9.
10.

Clinical and radiological outcome of patients suffering from chronic pancreatitis associated with gene mutations.

Frulloni L, Scattolini C, Graziani R, Cavestro GM, Pravadelli C, Amodio A, Manfredi R, Scarpa A, Vantini I.

Pancreas. 2008 Nov;37(4):371-6. doi: 10.1097/MPA.0b013e31817f52a1.

PMID:
18953248
11.

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. doi: 10.1097/MPG.0b013e31823f0269.

PMID:
22094894
12.

Mutations in the SPINK1 gene in idiopathic pancreatitis Italian patients.

Gomez-Lira M, Bonamini D, Castellani C, Unis L, Cavallini G, Assael BM, Pignatti PF.

Eur J Hum Genet. 2003 Jul;11(7):543-6.

13.

CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.

Tzetis M, Efthymiadou A, Strofalis S, Psychou P, Dimakou A, Pouliou E, Doudounakis S, Kanavakis E.

Hum Genet. 2001 Mar;108(3):216-21.

PMID:
11354633
14.

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. doi: 10.1097/MCG.0b013e3181a4e772.

PMID:
19593166
15.
16.

Cystic fibrosis gene mutations and pancreatitis risk: relation to epithelial ion transport and trypsin inhibitor gene mutations.

Noone PG, Zhou Z, Silverman LM, Jowell PS, Knowles MR, Cohn JA.

Gastroenterology. 2001 Dec;121(6):1310-9.

PMID:
11729110
17.

[Mutations of SPINK1 and PRSS1 gene in Korean patients with chronic pancreatitis].

Lee KH, Yoon WJ, Ryu JK, Kim YT, Yoon YB, Kim CY.

Korean J Gastroenterol. 2004 Aug;44(2):93-8. Korean.

18.

Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations.

Midha S, Khajuria R, Shastri S, Kabra M, Garg PK.

Gut. 2010 Jun;59(6):800-7. doi: 10.1136/gut.2009.191239.

PMID:
20551465
19.

Relevance of variants in serum antiproteinases for the course of chronic pancreatitis.

Teich N, Walther K, Bödeker H, Mössner J, Keim V.

Scand J Gastroenterol. 2002 Mar;37(3):360-5.

PMID:
11916201
20.

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. doi: 10.1016/j.jpedsurg.2009.05.023.

PMID:
19944211
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