Towards understanding microvillus inclusion disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s40348-016-0031-0.pdf
Reference34 articles.
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2. Phillips AD, Jenkins P, Raafat F, Walker-Smith JA (1985) Congenital microvillous atrophy: specific diagnostic features. Arch Dis Child 60(2):135–140
3. Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG (1989) Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation. N Engl J Med 320(10):646–651. doi: 10.1056/nejm198903093201006
4. Phillips AD, Schmitz J (1992) Familial microvillous atrophy: a clinicopathological survey of 23 cases. J Pediatr Gastroenterol Nutr 14(4):380–396
5. Phillips AD, Szafranski M, Man LY, Wall WJ (2000) Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies. J Pediatr Gastroenterol Nutr 30(1):34–42
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