Moroz SP - Search Results

1

Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.

Holzinger A, Maier EM, Bück C, Mayerhofer PU, Kappler M, Haworth JC, Moroz SP, Hadorn HB, Sadler JE, Roscher AA. Holzinger A, et al. Among authors: moroz sp. Am J Hum Genet. 2002 Jan;70(1):20-5. doi: 10.1086/338456. Epub 2001 Nov 21. Am J Hum Genet. 2002. PMID: 11719902 Free PMC article.

2

Celiac disease in a patient with a congenital deficiency of intestinal enteropeptidase.

Moroz SP, Hadorn B, Rossi TM, Haworth JC. Moroz SP, et al. Am J Gastroenterol. 2001 Jul;96(7):2251-4. doi: 10.1111/j.1572-0241.2001.03970.x. Am J Gastroenterol. 2001. PMID: 11467662

3

Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family.

Haworth JC, Demaugre F, Booth FA, Dilling LA, Moroz SP, Seshia SS, Seargeant LE, Coates PM. Haworth JC, et al. Among authors: moroz sp. J Pediatr. 1992 Oct;121(4):553-7. doi: 10.1016/s0022-3476(05)81143-6. J Pediatr. 1992. PMID: 1403388

4

Allelic association and linkage studies in Wilson disease.

Thomas GR, Roberts EA, Rosales TO, Moroz SP, Lambert MA, Wong LT, Cox DW. Thomas GR, et al. Among authors: moroz sp. Hum Mol Genet. 1993 Sep;2(9):1401-5. doi: 10.1093/hmg/2.9.1401. Hum Mol Genet. 1993. PMID: 7902160

5

The congenital intrahepatic arterioportal fistula syndrome: elucidation and proposed classification.

Norton SP, Jacobson K, Moroz SP, Culham G, Ng V, Turner J, John P. Norton SP, et al. Among authors: moroz sp. J Pediatr Gastroenterol Nutr. 2006 Aug;43(2):248-55. doi: 10.1097/01.mpg.0000221890.13630.ad. J Pediatr Gastroenterol Nutr. 2006. PMID: 16877994 Review.

6

Liver disease associated with alpha1-antitrypsin deficiency in childhood.

Moroz SP, Cutz E, Cox DW, Sass-Kortsak A. Moroz SP, et al. J Pediatr. 1976 Jan;88(1):19-25. doi: 10.1016/s0022-3476(76)80720-2. J Pediatr. 1976. PMID: 1082017

7

Floating-Harbor syndrome and celiac disease.

Chudley AE, Moroz SP. Chudley AE, et al. Among authors: moroz sp. Am J Med Genet. 1991 Mar 15;38(4):562-4. doi: 10.1002/ajmg.1320380413. Am J Med Genet. 1991. PMID: 2063899

8

Biliary atresia: the Canadian experience.

Schreiber RA, Barker CC, Roberts EA, Martin SR, Alvarez F, Smith L, Butzner JD, Wrobel I, Mack D, Moroz S, Rashid M, Persad R, Levesque D, Brill H, Bruce G, Critch J; Canadian Pediatric Hepatology Research Group. Schreiber RA, et al. J Pediatr. 2007 Dec;151(6):659-65, 665.e1. doi: 10.1016/j.jpeds.2007.05.051. Epub 2007 Oct 22. J Pediatr. 2007. PMID: 18035148

9

Membranoproliferative glomerulonephritis in childhood cirrhosis associated with alpha1-antitrypsin deficiency.

Moroz SP, Cutz E, Balfe JW, Sass-Kortsak A. Moroz SP, et al. Pediatrics. 1976 Feb;57(2):232-8. Pediatrics. 1976. PMID: 1082572

10

Acute pancreatitis in a patient with glutaric acidemia type I.

Lemire EG, Moroz S, Pollack B, Postuma R, Greenberg CR. Lemire EG, et al. J Pediatr. 1996 Apr;128(4):589-90. doi: 10.1016/s0022-3476(96)70383-9. J Pediatr. 1996. PMID: 8618204 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

20 results

Search Page