181 related articles for article (PubMed ID: 17784640)
1. Microvillus inclusion disease: progressive mucosal pathology. A scanning and transmission electron microscopic study, and thoughts about possible pathogenesis.
Poley JR
J Submicrosc Cytol Pathol; 2006; 38(2-3):125-36. PubMed ID: 17784640
[TBL] [Abstract][Full Text] [Related]
2. Microvillous inclusion disease: ultrastructural variability.
Iancu TC; Mahajnah M; Manov I; Shaoul R
Ultrastruct Pathol; 2007; 31(3):173-88. PubMed ID: 17613997
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 20505500
[TBL] [Abstract][Full Text] [Related]
4. Ultrastructural aspects of enterocyte defects in infancy and childhood.
Iancu TC; Manov I
Ultrastruct Pathol; 2010 May; 34(3):117-25. PubMed ID: 20455660
[TBL] [Abstract][Full Text] [Related]
5. [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; 146(31):1448-52. PubMed ID: 12190012
[TBL] [Abstract][Full Text] [Related]
6. Microvillous inclusion disease with abundant vermiform, electron-lucent vesicles.
Weeks DA; Zuppan CW; Malott RL; Mierau GW
Ultrastruct Pathol; 2003; 27(5):337-40. PubMed ID: 14708724
[TBL] [Abstract][Full Text] [Related]
7. Microvillous inclusion disease--an ultrastructural diagnosis: with a review of the literature.
Khubchandani SR; Vohra P; Chitale AR; Sidana P
Ultrastruct Pathol; 2011 Apr; 35(2):87-91. PubMed ID: 21299349
[TBL] [Abstract][Full Text] [Related]
8. The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Poley JR
Scanning Microsc; 1991 Dec; 5(4):1037-62; discussion 1062-3. PubMed ID: 1822028
[TBL] [Abstract][Full Text] [Related]
9. Microvillous atrophy: atypical presentations.
Perry A; Bensallah H; Martinez-Vinson C; Berrebi D; Arbeille B; Salomon J; Goulet O; Marinier E; Drunat S; Samson-Bouma ME; Gérard B; Hugot JP
J Pediatr Gastroenterol Nutr; 2014 Dec; 59(6):779-85. PubMed ID: 25111220
[TBL] [Abstract][Full Text] [Related]
10. [Ultrastructural changes in the intestinal mucosa of children with chronic diarrhea].
Jiang TA
Zhonghua Yi Xue Za Zhi; 1991 Feb; 71(2):68-71, 6. PubMed ID: 1647838
[TBL] [Abstract][Full Text] [Related]
11. Microvillous inclusion disease diagnosed by gastric biopsy.
Thomas N; Pulimood AB; Kumar M; Jana AK
Indian Pediatr; 2012 Jan; 49(1):58-60. PubMed ID: 22318102
[TBL] [Abstract][Full Text] [Related]
12. Microvillous inclusion disease: a clinicopathologic study of 17 cases from the UK.
Al-Daraji WI; Zelger B; Zelger B; Hussein MR
Ultrastruct Pathol; 2010 Dec; 34(6):327-32. PubMed ID: 21070163
[TBL] [Abstract][Full Text] [Related]
13. Microvillous inclusion disease. The importance of electron microscopy for diagnosis.
Bell SW; Kerner JA; Sibley RK
Am J Surg Pathol; 1991 Dec; 15(12):1157-64. PubMed ID: 1660676
[TBL] [Abstract][Full Text] [Related]
14. Scanning electron microscopy of soy protein-induced damage of small bowel mucosa in infants.
Poley JR; Klein AW
J Pediatr Gastroenterol Nutr; 1983 May; 2(2):271-87. PubMed ID: 6683755
[TBL] [Abstract][Full Text] [Related]
15. Microvillous inclusion disease (microvillous atrophy).
Ruemmele FM; Schmitz J; Goulet O
Orphanet J Rare Dis; 2006 Jun; 1():22. PubMed ID: 16800870
[TBL] [Abstract][Full Text] [Related]
16. [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. PubMed ID: 8114773
[TBL] [Abstract][Full Text] [Related]
17. Congenital Fatal Diarrhea in Newborns.
Lingaldinna S; Sundaram MB; Kamalarathnam CN; Bavanandam S
Indian J Pediatr; 2017 Dec; 84(12):953-954. PubMed ID: 28842815
[TBL] [Abstract][Full Text] [Related]
18. An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking.
Schneeberger K; Vogel GF; Teunissen H; van Ommen DD; Begthel H; El Bouazzaoui L; van Vugt AH; Beekman JM; Klumperman J; Müller T; Janecke A; Gerner P; Huber LA; Hess MW; Clevers H; van Es JH; Nieuwenhuis EE; Middendorp S
Proc Natl Acad Sci U S A; 2015 Oct; 112(40):12408-13. PubMed ID: 26392529
[TBL] [Abstract][Full Text] [Related]
19. Enterocyte apoptosis and proliferation are increased in microvillous inclusion disease (familial microvillous atrophy).
Groisman GM; Sabo E; Meir A; Polak-Charcon S
Hum Pathol; 2000 Nov; 31(11):1404-10. PubMed ID: 11112216
[TBL] [Abstract][Full Text] [Related]
20. MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome.
Golachowska MR; van Dael CM; Keuning H; Karrenbeld A; Hoekstra D; Gijsbers CF; Benninga MA; Rings EH; van Ijzendoorn SC
J Pediatr Gastroenterol Nutr; 2012 Apr; 54(4):491-8. PubMed ID: 22441677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]