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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1991 1
1992 1
1993 6
1994 3
1997 2
1998 2
1999 1
2000 1
2001 4
2002 4
2003 1
2004 3
2006 5
2007 3
2008 4
2010 6
2011 4
2012 4
2013 5
2014 10
2015 10
2016 10
2017 9
2018 5
2019 8
2020 4
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Similar Articles for PMID: 32873653

100 results
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Challenges of Microvillus Inclusion Disease in the NICU.
Badawy A, Elfadul M, Aziabi M, Ageel HI, Aqeel A. Badawy A, et al. Neoreviews. 2020 Sep;21(9):e600-e604. doi: 10.1542/neo.21-9-e600. Neoreviews. 2020. PMID: 32873653
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. Schneeberger K, et al. Proc Natl Acad Sci U S A. 2015 Oct 6;112(40):12408-13. doi: 10.1073/pnas.1516672112. Epub 2015 Sep 21. Proc Natl Acad Sci U S A. 2015. PMID: 26392529 Free PMC article.
Microvillous inclusion disease (microvillous atrophy).
Ruemmele FM, Schmitz J, Goulet O. Ruemmele FM, et al. Orphanet J Rare Dis. 2006 Jun 26;1:22. doi: 10.1186/1750-1172-1-22. Orphanet J Rare Dis. 2006. PMID: 16800870 Free PMC article. Review.
Towards understanding microvillus inclusion disease.
Vogel GF, Hess MW, Pfaller K, Huber LA, Janecke AR, Müller T. Vogel GF, et al. Mol Cell Pediatr. 2016 Dec;3(1):3. doi: 10.1186/s40348-016-0031-0. Epub 2016 Jan 29. Mol Cell Pediatr. 2016. PMID: 26830108 Free PMC article.
Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation.
Julia J, Shui V, Mittal N, Heim-Hall J, Blanco CL. Julia J, et al. J Neonatal Perinatal Med. 2019;12(3):313-319. doi: 10.3233/NPM-1852. J Neonatal Perinatal Med. 2019. PMID: 30909251
Loss of syntaxin 3 causes variant microvillus inclusion disease.
Wiegerinck CL, Janecke AR, Schneeberger K, Vogel GF, van Haaften-Visser DY, Escher JC, Adam R, Thöni CE, Pfaller K, Jordan AJ, Weis CA, Nijman IJ, Monroe GR, van Hasselt PM, Cutz E, Klumperman J, Clevers H, Nieuwenhuis EE, Houwen RH, van Haaften G, Hess MW, Huber LA, Stapelbroek JM, Müller T, Middendorp S. Wiegerinck CL, et al. Gastroenterology. 2014 Jul;147(1):65-68.e10. doi: 10.1053/j.gastro.2014.04.002. Epub 2014 Apr 12. Gastroenterology. 2014. PMID: 24726755
Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2-Deficient Intestinal Organoids.
Mosa MH, Nicolle O, Maschalidi S, Sepulveda FE, Bidaud-Meynard A, Menche C, Michels BE, Michaux G, de Saint Basile G, Farin HF. Mosa MH, et al. Cell Mol Gastroenterol Hepatol. 2018 Aug 14;6(4):477-493.e1. doi: 10.1016/j.jcmgh.2018.08.001. eCollection 2018. Cell Mol Gastroenterol Hepatol. 2018. PMID: 30364784 Free PMC article.
Recent advances in understanding and managing malabsorption: focus on microvillus inclusion disease.
Jayawardena D, Alrefai WA, Dudeja PK, Gill RK. Jayawardena D, et al. F1000Res. 2019 Dec 5;8:F1000 Faculty Rev-2061. doi: 10.12688/f1000research.20762.1. eCollection 2019. F1000Res. 2019. PMID: 31824659 Free PMC article. Review.
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. Perry A, et al. J Pediatr Gastroenterol Nutr. 2014 Dec;59(6):779-85. doi: 10.1097/MPG.0000000000000526. J Pediatr Gastroenterol Nutr. 2014. PMID: 25111220
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