Sacrosidase therapy for congenital sucrase-isomaltase deficiency

Journal of Pediatric Gastroenterology and Nutrition

Volumn 28, Issue 2, 1999, Pages 137-142

  Treem, William R ^a,c   McAdams, Luanne ^a   Stanford, Lesley ^a   Kastoff, Geraldine ^b   Justinich, Christopher ^b   Hyams, Jeffrey ^b  

^a DUKE UNIVERSITY   (United States)

^b Farmington   (United States)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Carbohydrate malabsorption; Disaccharidases; Sacrosidase; Sucrase isomaltase deficiency

Indexed keywords

DISACCHARIDASE; SACROSIDASE; SUCRASE ISOMALTASE; UNCLASSIFIED DRUG;

ABDOMINAL CRAMP; ARTICLE; BREATH ANALYSIS; CARBOHYDRATE INTOLERANCE; CHILD; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIARRHEA; DISEASE SEVERITY; DOSE RESPONSE; DOUBLE BLIND PROCEDURE; DRUG EFFICACY; DRUG SAFETY; ENZYME DEFICIENCY; GASTROINTESTINAL SYMPTOM; HUMAN; INFANT; PHASE 1 CLINICAL TRIAL; PHASE 2 CLINICAL TRIAL; PRIORITY JOURNAL; RANDOMIZED CONTROLLED TRIAL; WHEEZING;

ANIMALS; BREATH TESTS; CARBOHYDRATE METABOLISM, INBORN ERRORS; CHILD; CHILD, PRESCHOOL; DIARRHEA; DOUBLE-BLIND METHOD; HUMANS; HYDROGEN; INFANT; KINETICS; MILK; PLACEBOS; SACCHAROMYCES CEREVISIAE; SUCRASE; SUCRASE-ISOMALTASE COMPLEX; SUCROSE;

SACCHAROMYCES CEREVISIAE;

EID: 0033008474     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-199902000-00008     Document Type: Article

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