Microvillus inclusion disease: specific diagnostic features shown by alkaline phosphatase histochemistry.

Author:

Lake B D

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference12 articles.

1. Familial enteropathy: a syndrome of protracted diarrhoea from birth, failure to thrive and hypoplastic villus atrophy;Davidson, G.P.; Cutz, E.; Hamilton, JR, Gall; D.G.;Gastroenterology,1978

2. Congenital microvillus atrophy. A rare cause of neonatal intractable diarrhoea;Schmitz, J.; Ginies, J.L.; Arnaud-Battandier, F.;Pediatric Res,1982

3. A pathological condition due to congenital disorganisation of the brush border. In: Brush border membranes. CIBA Foundation Symposium;Schmitz, J.,1983

4. Congenital microvillous atrophy: specific diagnostic features;Phillips, A.D.; Jenkins, P.; Raafat, F.; Walker-Smith, J.A.;Arch Dis Child,1985

5. A tetrazolium method for non-specific alkaline phosphatase;McGadey, J.;Histochemie,1970

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