Congenital diarrhoeal disorders: Advances in this evolving web of inherited enteropathies

Nature Reviews Gastroenterology and Hepatology

Volumn 12, Issue 5, 2015, Pages 293-302

  Canani, Roberto Berni ^a   Castaldo, Giuseppe ^a   Bacchetta, Rosa ^b   Martín, Martín G ^c   Goulet, Olivier ^d  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c MATTEL CHILDREN S HOSPITAL   (United States)

^d UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DIACYLGLYCEROL ACYLTRANSFERASE 1; INTERLEUKIN 10; INTERLEUKIN 10 RECEPTOR;

ABSORPTION; CELL DIFFERENTIATION; CLINICAL FEATURE; CONGENITAL DIARRHEAL DISORDER; DEHYDRATION; DIARRHEA; DIGESTION; DISEASE SEVERITY; ELECTROLYTE DISTURBANCE; ENTEROENDOCRINE CELL; ENTEROPATHY; ERYTHROMELALGIA; GENE MUTATION; HUMAN; INTESTINE CELL; IPEX SYNDROME; MICROVILLUS; MOLECULAR DIAGNOSIS; MOLECULAR GENETICS; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; SYSTEMIC DISEASE; CHRONIC DISEASE; GENETICS; INTESTINAL DISEASES; PATHOPHYSIOLOGY;

CHRONIC DISEASE; DIARRHEA; HUMANS; INTESTINAL DISEASES;

EID: 84929702339     PISSN: 17595045     EISSN: 17595053     Source Type: Journal    
DOI: 10.1038/nrgastro.2015.44     Document Type: Review

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