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Items: 1 to 20 of 79

1.

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

Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG.

N Engl J Med. 1989 Mar 9;320(10):646-51. No abstract available.

PMID:
2537465
2.

Congenital microvillus atrophy in a 4-month-old girl.

Acar Y, Ertem D, Ozg├╝ven E, Okar I, Ahiskali R, Pehlivano─člu E.

Turk J Pediatr. 1999 Oct-Dec;41(4):495-500.

PMID:
10770118
3.

Microvillous inclusion disease. The importance of electron microscopy for diagnosis.

Bell SW, Kerner JA Jr, Sibley RK.

Am J Surg Pathol. 1991 Dec;15(12):1157-64.

PMID:
1660676
5.

Gastrointestinal microvillus inclusion disease.

Schofield DE, Agostini RM Jr, Yunis EJ.

Am J Clin Pathol. 1992 Jul;98(1):119-24. Review.

PMID:
1319670
6.

[Congenital villous atrophy. Disease picture of congenital chronic diarrhea with poor prognosis].

Cegla M, Lohner M, Schaefer HE.

Monatsschr Kinderheilkd. 1993 Dec;141(12):925-7. German.

PMID:
8114773
7.

[Microvillus inclusion disease, a rare cause of severe congenital diarrhea].

Jacobs MJ, Tolboom JJ, Bosman DK, van Haelst UJ, Bult P, Kneepkens CM, Taminiau JA.

Ned Tijdschr Geneeskd. 2002 Aug 3;146(31):1448-52. Review. Dutch.

PMID:
12190012
8.

Abnormal expression of brush-border membrane transporters in the duodenal mucosa of two patients with microvillus inclusion disease.

Michail S, Collins JF, Xu H, Kaufman S, Vanderhoof J, Ghishan FK.

J Pediatr Gastroenterol Nutr. 1998 Nov;27(5):536-42.

PMID:
9822319
9.

Microvillous inclusion disease: ultrastructural variability.

Iancu TC, Mahajnah M, Manov I, Shaoul R.

Ultrastruct Pathol. 2007 May-Jun;31(3):173-88.

PMID:
17613997
10.

Increased paracellular macromolecular transport and subnormal glucose uptake in duodenal biopsies of patients with microvillus inclusion disease. Comparisons to other chronic diarrhea patients and to nondiarrhea patients.

Bijlsma PB, Kiliaan AJ, Scholten G, van der Wal A, Heyman M, Heymans HS, Groot JA, Taminiau JA.

Ann N Y Acad Sci. 2000;915:267-9. No abstract available.

PMID:
11193585
11.

Congenital microvillous atrophy: report of two cases.

Steininger H, Behrens R, Faller G, Schindler C, Kirchner T.

Gen Diagn Pathol. 1997 Feb;142(3-4):217-20.

PMID:
9065586
12.
13.

Ultrastructural aspects of enterocyte defects in infancy and childhood.

Iancu TC, Manov I.

Ultrastruct Pathol. 2010 May;34(3):117-25. doi: 10.3109/01913121003648410. Review.

PMID:
20455660
15.

Microvillous inclusion disease in Japan.

Kaneko K, Shimizu T, Fujiwara S, Igarashi J, Ohtomo Y, Yamashiro Y.

J Pediatr. 1999 Sep;135(3):400. No abstract available.

PMID:
10484813
16.

Light microscopic diagnosis of microvillus inclusion disease on colorectal specimens using CD10.

Koepsell SA, Talmon G.

Am J Surg Pathol. 2010 Jul;34(7):970-2. doi: 10.1097/PAS.0b013e3181e11e4b.

PMID:
20505500
17.

Microvillous inclusion disease with abundant vermiform, electron-lucent vesicles.

Weeks DA, Zuppan CW, Malott RL, Mierau GW.

Ultrastruct Pathol. 2003 Sep-Oct;27(5):337-40.

PMID:
14708724
19.

Microvillus inclusion disease associated with coarctation of the aorta and bicuspid aortic valve.

Gathungu GN, Pashankar DS, Sarita-Reyes CD, Zambrano E, Reyes-Mugica M, Brueckner M, Mistry PK, Husain SZ.

J Clin Gastroenterol. 2008 Apr;42(4):400-3. doi: 10.1097/01.mcg.0000225632.07039.b6.

PMID:
18277898
20.

Microvillous inclusion disease: an evolving condition.

Croft NM, Howatson AG, Ling SC, Nairn L, Evans TJ, Weaver LT.

J Pediatr Gastroenterol Nutr. 2000 Aug;31(2):185-9. No abstract available.

PMID:
10941974

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