275 related articles for article (PubMed ID: 18572020)
21. Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy.
Bodian DL; Vilboux T; Hourigan SK; Jenevein CL; Mani H; Kent KC; Khromykh A; Solomon BD; Hauser NS
Cold Spring Harb Mol Case Stud; 2017 Nov; 3(6):. PubMed ID: 28701297
[TBL] [Abstract][Full Text] [Related]
22. Tufting enteropathy and chronic arthritis: a newly recognized association with a novel EpCAM gene mutation.
Al-Mayouf SM; Alswaied N; Alkuraya FS; Almehaidib A; Faqih M
J Pediatr Gastroenterol Nutr; 2009 Nov; 49(5):642-4. PubMed ID: 19820410
[No Abstract] [Full Text] [Related]
23. Frequency of rearrangements in Lynch syndrome cases associated with MSH2: characterization of a new deletion involving both EPCAM and the 5' part of MSH2.
Pérez-Cabornero L; Infante Sanz M; Velasco Sampedro E; Lastra Aras E; Acedo Becares A; Miner Pino C; Durán Domínguez M
Cancer Prev Res (Phila); 2011 Oct; 4(10):1556-62. PubMed ID: 21791569
[TBL] [Abstract][Full Text] [Related]
24. Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
Güvenoğlu M; Şimşek-Kiper PÖ; Koşukcu C; Taskiran EZ; Saltık-Temizel İN; Gucer S; Utine E; Boduroğlu K
Pediatr Gastroenterol Hepatol Nutr; 2022 Nov; 25(6):441-452. PubMed ID: 36451688
[TBL] [Abstract][Full Text] [Related]
25. New mutations of
AlMahamed S; Hammo A
Saudi J Gastroenterol; 2017; 23(2):123-126. PubMed ID: 28361844
[TBL] [Abstract][Full Text] [Related]
26. Further evidence for EpCAM as the gene for congenital tufting enteropathy.
Sivagnanam M; Schaible T; Szigeti R; Byrd RH; Finegold MJ; Ranganathan S; Gopalakrishna GS; Tatevian N; Kellermayer R
Am J Med Genet A; 2010 Jan; 152A(1):222-4. PubMed ID: 20034091
[No Abstract] [Full Text] [Related]
27. Chronic enteropathy: molecular basis.
Ruemmele FM
Nestle Nutr Workshop Ser Pediatr Program; 2007; 59():73-85; discussion 85-8. PubMed ID: 17245092
[TBL] [Abstract][Full Text] [Related]
28. Congenital Tufting Enteropathy: Biology, Pathogenesis and Mechanisms.
Das B; Sivagnanam M
J Clin Med; 2020 Dec; 10(1):. PubMed ID: 33374714
[TBL] [Abstract][Full Text] [Related]
29. [The congenital tufting enteropathy, or when the intestine is under low cellular tension].
Gaston C; Salomon J; Goulet O; Delacour D
Med Sci (Paris); 2017; 33(8-9):694-697. PubMed ID: 28945548
[No Abstract] [Full Text] [Related]
30. 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. PubMed ID: 20981223
[TBL] [Abstract][Full Text] [Related]
31. A novel nonsense mutation in CEP290 induces exon skipping and leads to a relatively mild retinal phenotype.
Littink KW; Pott JW; Collin RW; Kroes HY; Verheij JB; Blokland EA; de Castro Miró M; Hoyng CB; Klaver CC; Koenekoop RK; Rohrschneider K; Cremers FP; van den Born LI; den Hollander AI
Invest Ophthalmol Vis Sci; 2010 Jul; 51(7):3646-52. PubMed ID: 20130272
[TBL] [Abstract][Full Text] [Related]
32. Kocuria kristinae-caused sepsis in an infant with congenital tufting enteropathy.
Aydin M; Ganschow R; Jankofsky M
Turk J Pediatr; 2017; 59(1):93-96. PubMed ID: 29168373
[TBL] [Abstract][Full Text] [Related]
33. Identification of a Japanese Lynch syndrome patient with large deletion in the 3' region of the EPCAM gene.
Eguchi H; Kumamoto K; Suzuki O; Kohda M; Tada Y; Okazaki Y; Ishida H
Jpn J Clin Oncol; 2016 Feb; 46(2):178-84. PubMed ID: 26613680
[TBL] [Abstract][Full Text] [Related]
34. Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy.
Yanamoto S; Kawasaki G; Yoshitomi I; Iwamoto T; Hirata K; Mizuno A
Oral Oncol; 2007 Oct; 43(9):869-77. PubMed ID: 17207659
[TBL] [Abstract][Full Text] [Related]
35. 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. PubMed ID: 20447614
[TBL] [Abstract][Full Text] [Related]
36. Intestinal epithelial dysplasia (tufting enteropathy).
Goulet O; Salomon J; Ruemmele F; de Serres NP; Brousse N
Orphanet J Rare Dis; 2007 Apr; 2():20. PubMed ID: 17448233
[TBL] [Abstract][Full Text] [Related]
37. A Novel Compound-Heterozygous Epithelial Cell Adhesion Molecule Mutation in Tufting Enteropathy.
Shakhnovich V; Dinwiddie D; Hildreth A; Attard T; Kingsmore S
J Pediatr Gastroenterol Nutr; 2017 Jan; 64(1):e14-e16. PubMed ID: 25383784
[No Abstract] [Full Text] [Related]
38. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
Cohen D; Bar-Yosef U; Levy J; Gradstein L; Belfair N; Ofir R; Joshua S; Lifshitz T; Carmi R; Birk OS
Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
[TBL] [Abstract][Full Text] [Related]
39. A case of severe malnutrition infant with neonatal onset intractable diarrhea.
Fang Y; Luo Y; Yu J; Chen J
BMC Pediatr; 2020 Mar; 20(1):133. PubMed ID: 32293360
[TBL] [Abstract][Full Text] [Related]
40. Single nucleotide polymorphisms of the EpCAM-coding gene TACSTD1 in patients with ovarian cancer and their potential translational aspects.
Heubner M; Wimberger P; Kasimir-Bauer S; Singer BB; Ruf P; Kimmig R; Siffert W
Arch Gynecol Obstet; 2015 Dec; 292(6):1367-72. PubMed ID: 26115884
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
