用于簇绒性肠病的孤立性小肠移植 - Suppr

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Isolated small bowel transplantation for tufting enteropathy.

作者信息

Paramesh Anil S, Fishbein Thomas, Tschernia Allan, Leleiko Neil, Magid Margret S, Gondolesi Gabriel E, Kaufman Stuart S

机构信息

The Recanati Miller Transplantation Institute, Sinai School of Medicine, New York, New York 10029, USA.

出版信息

J Pediatr Gastroenterol Nutr. 2003 Jan;36(1):138-40. doi: 10.1097/00005176-200301000-00026.

DOI:10.1097/00005176-200301000-00026

PMID:12500010

Abstract

摘要

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Isolated small bowel transplantation for tufting enteropathy.

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引用本文的文献

[A Case of Congenital Tufting Enteropathy with Gene Complex Heterozygous Mutation (c.491+1G>A; c.352_353ins CACC)].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 May;53(3):493-496. doi: 10.12182/20220560109.

Tufting Enteropathy: A Review of Clinical and Histological Presentation, Etiology, Management, and Outcome.

Gastroenterol Res Pract. 2020 Sep 23;2020:5608069. doi: 10.1155/2020/5608069. eCollection 2020.

A case of severe malnutrition infant with neonatal onset intractable diarrhea.

BMC Pediatr. 2020 Mar 23;20(1):133. doi: 10.1186/s12887-020-1999-0.

Enteroids expressing a disease-associated mutant of EpCAM are a model for congenital tufting enteropathy.

Am J Physiol Gastrointest Liver Physiol. 2019 Nov 1;317(5):G580-G591. doi: 10.1152/ajpgi.00098.2019. Epub 2019 Aug 21.

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.

Hum Mutat. 2019 Feb;40(2):142-161. doi: 10.1002/humu.23688. Epub 2018 Nov 29.

Identification of mutation: clinical use of microarray.

Clin Case Rep. 2017 May 10;5(6):980-985. doi: 10.1002/ccr3.914. eCollection 2017 Jun.

New mutations of gene for tufting enteropathy in Saudi Arabia.

Saudi J Gastroenterol. 2017 Mar-Apr;23(2):123-126. doi: 10.4103/1319-3767.203359.

Functional consequences of EpCam mutation in mice and men.

Am J Physiol Gastrointest Liver Physiol. 2014 Feb 15;306(4):G278-88. doi: 10.1152/ajpgi.00286.2013. Epub 2013 Dec 12.

Tufting Enteropathy with EpCAM Mutations in Two Siblings.

Gut Liver. 2010 Sep;4(3):407-10. doi: 10.5009/gnl.2010.4.3.407. Epub 2010 Sep 24.

Identification of EpCAM as the gene for congenital tufting enteropathy.

Gastroenterology. 2008 Aug;135(2):429-37. doi: 10.1053/j.gastro.2008.05.036. Epub 2008 May 15.

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相似文献

Isolated small bowel transplantation for tufting enteropathy.

J Pediatr Gastroenterol Nutr. 2003 Jan;36(1):138-40. doi: 10.1097/00005176-200301000-00026.

[Small intestine transplant for intestinal failure in children].

Ugeskr Laeger. 2010 Mar 15;172(11):883-5.

[The first Danish child with small bowel transplantation].

Ugeskr Laeger. 2010 Mar 15;172(11):886-7.

Liver and small bowel transplantation: therapeutic alternatives for the treatment of liver disease and intestinal failure.

Semin Liver Dis. 2000;20(4):437-50. doi: 10.1055/s-2000-13151.

Intestinal transplantation in humans under FK 506.

Transplant Proc. 1993 Feb;25(1 Pt 2):1198-9.

Preliminary experience with combined liver and small bowel transplantation in children.

Transplant Proc. 1998 Sep;30(6):2526-7. doi: 10.1016/s0041-1345(98)00710-6.

Small bowel and liver/small bowel transplantation in children.

Semin Pediatr Surg. 1993 Nov;2(4):289-300.

Intestinal transplantation in children.

Transplant Proc. 1996 Oct;28(5):2752.

Small bowel transplantation. A life-saving option for selected patients with intestinal failure.

Dig Dis Sci. 1996 May;41(5):875-83. doi: 10.1007/BF02091526.

[Intestinal transplantation--an experimental therapy which has become a realistic alternative].

Lakartidningen. 2004 Sep 16;101(38):2874-8.

引用本文的文献

[A Case of Congenital Tufting Enteropathy with Gene Complex Heterozygous Mutation (c.491+1G>A; c.352_353ins CACC)].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 May;53(3):493-496. doi: 10.12182/20220560109.

Tufting Enteropathy: A Review of Clinical and Histological Presentation, Etiology, Management, and Outcome.

Gastroenterol Res Pract. 2020 Sep 23;2020:5608069. doi: 10.1155/2020/5608069. eCollection 2020.

A case of severe malnutrition infant with neonatal onset intractable diarrhea.

BMC Pediatr. 2020 Mar 23;20(1):133. doi: 10.1186/s12887-020-1999-0.

Enteroids expressing a disease-associated mutant of EpCAM are a model for congenital tufting enteropathy.

Am J Physiol Gastrointest Liver Physiol. 2019 Nov 1;317(5):G580-G591. doi: 10.1152/ajpgi.00098.2019. Epub 2019 Aug 21.

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.

Hum Mutat. 2019 Feb;40(2):142-161. doi: 10.1002/humu.23688. Epub 2018 Nov 29.

Identification of mutation: clinical use of microarray.

Clin Case Rep. 2017 May 10;5(6):980-985. doi: 10.1002/ccr3.914. eCollection 2017 Jun.

New mutations of gene for tufting enteropathy in Saudi Arabia.

Saudi J Gastroenterol. 2017 Mar-Apr;23(2):123-126. doi: 10.4103/1319-3767.203359.

Functional consequences of EpCam mutation in mice and men.

Am J Physiol Gastrointest Liver Physiol. 2014 Feb 15;306(4):G278-88. doi: 10.1152/ajpgi.00286.2013. Epub 2013 Dec 12.

Tufting Enteropathy with EpCAM Mutations in Two Siblings.

Gut Liver. 2010 Sep;4(3):407-10. doi: 10.5009/gnl.2010.4.3.407. Epub 2010 Sep 24.

Identification of EpCAM as the gene for congenital tufting enteropathy.

Gastroenterology. 2008 Aug;135(2):429-37. doi: 10.1053/j.gastro.2008.05.036. Epub 2008 May 15.