A newborn infant with protracted diarrhea and metabolic acidosis.

[1]  M. Tsai,et al.  Mutant neurogenin-3 in congenital malabsorptive diarrhea. , 2006, The New England journal of medicine.

[2]  A. Phillips.  Diarrhées intraitables dues à des anomalies congénitales des entérocytes , 2006, Annales Nestlé (Ed. française).

[3]  Vann Schaffner,et al.  Small bowel biopsy in a 6-week-old infant. Microvillous inclusion disease of the small intestine. , 2006, Archives of pathology & laboratory medicine.

[4]  A. Phillips.  Intractable Diarrhoea due to Congenital Enterocyte Defects , 2005, Annales Nestlé (English ed.).

[5]  G. Schwartz,et al.  Back to basics: acidosis and alkalosis. , 2004, Pediatrics in review.

[6]  Y. Révillon,et al.  NEW PERSPECTIVES FOR CHILDREN WITH MICROVILLOUS INCLUSION DISEASE: EARLY SMALL BOWEL TRANSPLANTATION , 2004, Transplantation.

[7]  P. Sherman,et al.  Neonatal Enteropathies: Defining the Causes of Protracted Diarrhea of Infancy , 2004, Journal of pediatric gastroenterology and nutrition.

[8]  C. Zuppan,et al.  Microvillous Inclusion Disease with Abundant Vermiform, Electron-Lucent Vesicles , 2003, Ultrastructural pathology.

[9]  H. Naim,et al.  Autophagocytosis of the apical membrane in microvillus inclusion disease , 2002, Gut.

[10]  J. Soriano,et al.  Renal tubular acidosis: the clinical entity. , 2002, Journal of the American Society of Nephrology : JASN.

[11]  G. Groisman,et al.  CD10: A Valuable Tool for the Light Microscopic Diagnosis of Microvillous Inclusion Disease (Familial Microvillous Atrophy) , 2002, The American journal of surgical pathology.

[12]  F. Gottrand,et al.  Neonatal severe intractable diarrhoea as the presenting manifestation of an unclassified congenital disorder of glycosylation (CDG-x) , 2001, Archives of disease in childhood. Fetal and neonatal edition.

[13]  A. Phillips,et al.  Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies. , 2000, Journal of pediatric gastroenterology and nutrition.

[14]  J. Pohl,et al.  A cluster of microvillous inclusion disease in the Navajo population. , 1999, The Journal of pediatrics.

[15]  S. Koletzko,et al.  Congenital enterocyte heparan sulphate deficiency with massive albumin loss, secretory diarrhoea, and malnutrition , 1996, The Lancet.

[16]  A. Phillips,et al.  Familial Microvillous Atrophy: A Clinicopathological Survey of 23 Cases , 1992, Journal of pediatric gastroenterology and nutrition.

[17]  N. Brousse,et al.  Classification of intractable diarrhea in infancy using clinical and immunohistological criteria. , 1990, Gastroenterology.

[18]  B. Lake.  Microvillus inclusion disease: specific diagnostic features shown by alkaline phosphatase histochemistry. , 1988, Journal of clinical pathology.

[19]  F. Raafat,et al.  Congenital microvillous atrophy: specific diagnostic features. , 1985, Archives of disease in childhood.

[20]  E. Cutz,et al.  Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy , 1978 .

[21]  Hal B. Jenson,et al.  Nelson Textbook of Pediatrics , 1965 .