Durie PR - Search Results

1

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation.

Gallinger S, Aronson M, Shayan K, Ratcliffe EM, Gerstle JT, Parkin PC, Rothenmund H, Croitoru M, Baumann E, Durie PR, Weksberg R, Pollett A, Riddell RH, Ngan BY, Cutz E, Lagarde AE, Chan HS. Gallinger S, et al. Among authors: durie pr. Gastroenterology. 2004 Feb;126(2):576-85. doi: 10.1053/j.gastro.2003.11.008. Gastroenterology. 2004. PMID: 14762794

2

Congenital cholesteatoma in a child carrying a gene mutation for adenomatous polyposis coli.

Shaoul R, Papsin B, Cutz E, Durie P. Shaoul R, et al. J Pediatr Gastroenterol Nutr. 1999 Jan;28(1):100-3. doi: 10.1097/00005176-199901000-00023. J Pediatr Gastroenterol Nutr. 1999. PMID: 9890479 No abstract available.

3

Cardiac rhabdomyomata and megacystis-microcolon-intestinal hypoperistalsis syndrome.

Couper RT, Byard RW, Cutz E, Stringer DA, Durie PR. Couper RT, et al. Among authors: durie pr. J Med Genet. 1991 Apr;28(4):274-6. doi: 10.1136/jmg.28.4.274. J Med Genet. 1991. PMID: 1856835 Free PMC article.

4

Deficiency of Sbds in the mouse pancreas leads to features of Shwachman-Diamond syndrome, with loss of zymogen granules.

Tourlakis ME, Zhong J, Gandhi R, Zhang S, Chen L, Durie PR, Rommens JM. Tourlakis ME, et al. Among authors: durie pr. Gastroenterology. 2012 Aug;143(2):481-92. doi: 10.1053/j.gastro.2012.04.012. Epub 2012 Apr 14. Gastroenterology. 2012. PMID: 22510201

5

The radiologic and endoscopic investigation and etiologic classification of gastritis in children.

Manson DE, Stringer DA, Durie PR, Cutz E. Manson DE, et al. Among authors: durie pr. Can Assoc Radiol J. 1990 Aug;41(4):201-6. Can Assoc Radiol J. 1990. PMID: 2207775

6

Management of fibrosing pancreatitis in children presenting with obstructive jaundice.

Sylvester FA, Shuckett B, Cutz E, Durie PR, Marcon MA. Sylvester FA, et al. Among authors: durie pr. Gut. 1998 Nov;43(5):715-20. doi: 10.1136/gut.43.5.715. Gut. 1998. PMID: 9824357 Free PMC article.

7

Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation.

Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG. Cutz E, et al. Among authors: durie pr. N Engl J Med. 1989 Mar 9;320(10):646-51. doi: 10.1056/NEJM198903093201006. N Engl J Med. 1989. PMID: 2537465 No abstract available.

8

Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.

Ooi CY, Dorfman R, Cipolli M, Gonska T, Castellani C, Keenan K, Freedman SD, Zielenski J, Berthiaume Y, Corey M, Schibli S, Tullis E, Durie PR. Ooi CY, et al. Among authors: durie pr. Gastroenterology. 2011 Jan;140(1):153-61. doi: 10.1053/j.gastro.2010.09.046. Epub 2010 Nov 9. Gastroenterology. 2011. PMID: 20923678

9

Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression.

Mack DR, Forstner GG, Wilschanski M, Freedman MH, Durie PR. Mack DR, et al. Among authors: durie pr. Gastroenterology. 1996 Dec;111(6):1593-602. doi: 10.1016/s0016-5085(96)70022-7. Gastroenterology. 1996. PMID: 8942739

10

Assessment of the efficacy of in vivo CFTR protein replacement therapy in CF mice.

Ramjeesingh M, Huan LJ, Wilschanski M, Durie P, Li C, Gyomorey K, Wang Y, Kent G, Tanswell KA, Cutz E, Ackerley C, Bear CE. Ramjeesingh M, et al. Hum Gene Ther. 1998 Mar 1;9(4):521-8. doi: 10.1089/hum.1998.9.4-521. Hum Gene Ther. 1998. PMID: 9525313

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