Whitcomb DC - Search Results

1

Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.

Orenstein SR, Shalaby TM, Finch R, Pfuetzer RH, DeVandry S, Chensny LJ, Bannada MM, Whitcomb DC. Orenstein SR, et al. Among authors: whitcomb dc. Am J Gastroenterol. 2002 Nov;97(11):2725-32. doi: 10.1111/j.1572-0241.2002.07060.x. Am J Gastroenterol. 2002. PMID: 12425539

2

Chronic abdominal pain caused by thoracic disc herniation.

Whitcomb DC, Martin SP, Schoen RE, Jho HD. Whitcomb DC, et al. Am J Gastroenterol. 1995 May;90(5):835-7. Am J Gastroenterol. 1995. PMID: 7733103

3

A gene for hereditary pancreatitis maps to chromosome 7q35.

Whitcomb DC, Preston RA, Aston CE, Sossenheimer MJ, Barua PS, Zhang Y, Wong-Chong A, White GJ, Wood PG, Gates LK Jr, Ulrich C, Martin SP, Post JC, Ehrlich GD. Whitcomb DC, et al. Gastroenterology. 1996 Jun;110(6):1975-80. doi: 10.1053/gast.1996.v110.pm8964426. Gastroenterology. 1996. PMID: 8964426

4

Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG).

Sossenheimer MJ, Aston CE, Preston RA, Gates LK Jr, Ulrich CD, Martin SP, Zhang Y, Gorry MC, Ehrlich GD, Whitcomb DC. Sossenheimer MJ, et al. Among authors: whitcomb dc. Am J Gastroenterol. 1997 Jul;92(7):1113-6. Am J Gastroenterol. 1997. PMID: 9219780

5

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.

Gorry MC, Gabbaizedeh D, Furey W, Gates LK Jr, Preston RA, Aston CE, Zhang Y, Ulrich C, Ehrlich GD, Whitcomb DC. Gorry MC, et al. Among authors: whitcomb dc. Gastroenterology. 1997 Oct;113(4):1063-8. doi: 10.1053/gast.1997.v113.pm9322498. Gastroenterology. 1997. PMID: 9322498

6

SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis.

Pfützer RH, Barmada MM, Brunskill AP, Finch R, Hart PS, Neoptolemos J, Furey WF, Whitcomb DC. Pfützer RH, et al. Among authors: whitcomb dc. Gastroenterology. 2000 Sep;119(3):615-23. doi: 10.1053/gast.2000.18017. Gastroenterology. 2000. PMID: 10982753

7

Chronic pancreatitis: diagnosis, classification, and new genetic developments.

Etemad B, Whitcomb DC. Etemad B, et al. Among authors: whitcomb dc. Gastroenterology. 2001 Feb;120(3):682-707. doi: 10.1053/gast.2001.22586. Gastroenterology. 2001. PMID: 11179244 Review.

8

Motivations and concerns of patients with access to genetic testing for hereditary pancreatitis.

Applebaum-Shapiro SE, Peters JA, O'Connell JA, Aston CE, Whitcomb DC. Applebaum-Shapiro SE, et al. Among authors: whitcomb dc. Am J Gastroenterol. 2001 May;96(5):1610-7. doi: 10.1111/j.1572-0241.2001.03787.x. Am J Gastroenterol. 2001. PMID: 11374708

9

Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.

Pfützer R, Myers E, Applebaum-Shapiro S, Finch R, Ellis I, Neoptolemos J, Kant JA, Whitcomb DC. Pfützer R, et al. Among authors: whitcomb dc. Gut. 2002 Feb;50(2):271-2. doi: 10.1136/gut.50.2.271. Gut. 2002. PMID: 11788572 Free PMC article.

10

Genetics of gastroesophageal reflux disease: a review.

Orenstein SR, Shalaby TM, Barmada MM, Whitcomb DC. Orenstein SR, et al. Among authors: whitcomb dc. J Pediatr Gastroenterol Nutr. 2002 May;34(5):506-10. doi: 10.1097/00005176-200205000-00005. J Pediatr Gastroenterol Nutr. 2002. PMID: 12050574 Review. No abstract available.

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