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Items: 1 to 20 of 103

1.

Tufting enteropathy revisited: the utility of MOC31 (EpCAM) immunohistochemistry in diagnosis.

Ranganathan S, Schmitt LA, Sindhi R.

Am J Surg Pathol. 2014 Feb;38(2):265-72. doi: 10.1097/PAS.0000000000000106.

PMID:
24418860
2.

Evaluation of intestinal biopsies for pediatric enteropathy: a proposed immunohistochemical panel approach.

Martin BA, Kerner JA, Hazard FK, Longacre TA.

Am J Surg Pathol. 2014 Oct;38(10):1387-95. doi: 10.1097/PAS.0000000000000314.

PMID:
25188866
3.

A novel nonsense mutation in the EpCAM gene in a patient with congenital tufting enteropathy.

Thoeni C, Amir A, Guo C, Zhang S, Avitzur Y, Heng YM, Cutz E, Muise AM.

J Pediatr Gastroenterol Nutr. 2014 Jan;58(1):18-21. doi: 10.1097/MPG.0000000000000106.

PMID:
24048167
4.

Features of gastric and colonic mucosa in congenital enteropathies: a study in histology and immunohistochemistry.

Treetipsatit J, Hazard FK.

Am J Surg Pathol. 2014 Dec;38(12):1697-706. doi: 10.1097/PAS.0000000000000287.

PMID:
25007148
5.

mTrop1/Epcam knockout mice develop congenital tufting enteropathy through dysregulation of intestinal E-cadherin/β-catenin.

Guerra E, Lattanzio R, La Sorda R, Dini F, Tiboni GM, Piantelli M, Alberti S.

PLoS One. 2012;7(11):e49302. doi: 10.1371/journal.pone.0049302. Epub 2012 Nov 28. Erratum in: PLoS One. 2013;8(5). doi:10.1371/annotation/4336e050-68c3-48ef-869e-80c2232b7e65.

6.

Functional consequences of EpCam mutation in mice and men.

Mueller JL, McGeough MD, Peña CA, Sivagnanam M.

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

7.

Identification of EpCAM as the gene for congenital tufting enteropathy.

Sivagnanam M, Mueller JL, Lee H, Chen Z, Nelson SF, Turner D, Zlotkin SH, Pencharz PB, Ngan BY, Libiger O, Schork NJ, Lavine JE, Taylor S, Newbury RO, Kolodner RD, Hoffman HM.

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

8.

Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form.

Salomon J, Goulet O, Canioni D, Brousse N, Lemale J, Tounian P, Coulomb A, Marinier E, Hugot JP, Ruemmele F, Dufier JL, Roche O, Bodemer C, Colomb V, Talbotec C, Lacaille F, Campeotto F, Cerf-Bensussan N, Janecke AR, Mueller T, Koletzko S, Bonnefont JP, Lyonnet S, Munnich A, Poirier F, Smahi A.

Hum Genet. 2014 Mar;133(3):299-310. doi: 10.1007/s00439-013-1380-6. Epub 2013 Oct 19.

PMID:
24142340
9.

[Tufting enteropathy: a case report, histopathological methodology, and differential diagnoses].

Bosaleh A, Contreras M, García de Dávila MT.

Acta Gastroenterol Latinoam. 2015 Mar;45(1):65-9. Spanish.

PMID:
26076517
10.

A rare cause of congenital diarrhea in a Turkish newborn: tufting enteropathy.

Kahvecioğlu D, Yıldız D, Kılıç A, İnce-Alkan B, Erdeve Ö, Kuloğlu Z, Atasay B, Ensari A, Yılmaz R, Arsan S.

Turk J Pediatr. 2014 Jul-Aug;56(4):440-3.

PMID:
25818968
11.

Superficial punctate keratitis and conjunctival erosions associated with congenital tufting enteropathy.

Roche O, Putterman M, Salomon J, Lacaille F, Brousse N, Goulet O, Dufier JL.

Am J Ophthalmol. 2010 Jul;150(1):116-121.e1. doi: 10.1016/j.ajo.2010.01.034. Epub 2010 May 5.

PMID:
20447614
12.

Small intestinal mucosal fat in childhood enteropathies.

Variend S, Placzek M, Raafat F, Walker-Smith JA.

J Clin Pathol. 1984 Apr;37(4):373-7.

13.

Tufting Enteropathy with EpCAM Mutations in Two Siblings.

Ko JS, Seo JK, Shim JO, Hwang SH, Park HS, Kang GH.

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

14.

Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy.

Davidson GP, Cutz E, Hamilton JR, Gall DG.

Gastroenterology. 1978 Nov;75(5):783-90.

PMID:
100367
15.

Intractable diarrhea with tufting enteropathy: a favorable outcome is possible.

Lemale J, Coulomb A, Dubern B, Boudjemaa S, Viola S, Josset P, Tounian P, Girardet JP.

J Pediatr Gastroenterol Nutr. 2011 Jun;52(6):734-9. doi: 10.1097/MPG.0b013e31820731db.

PMID:
21478758
16.

[Clinical studies of pediatric malabsorption syndromes].

Hosoyamada T.

Fukuoka Igaku Zasshi. 2006 Nov;97(11):322-50. Japanese.

PMID:
17228786
17.

Perinodular ductular reaction/epithelial cell adhesion molecule loss in small hepatic nodules.

Zhang Q, Zhang CS, Xin Q, Ma Z, Liu GQ, Liu BB, Wang FM, Gao YT, Du Z.

World J Gastroenterol. 2014 Aug 21;20(31):10908-15. doi: 10.3748/wjg.v20.i31.10908.

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20.

[Rotavirus and malabsorption. Immunofluorescence microscopy studies of small intestine specimens].

Fiehring C, Körting HJ, Jung G.

Dtsch Z Verdau Stoffwechselkr. 1984;44(1):1-5. German.

PMID:
6368189

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