Relationships among Dietary Intakes and Persistent Gastrointestinal Symptoms in Patients Receiving Enzyme Treatment for Genetic Sucrase-Isomaltase Deficiency
Author:
Publisher
Elsevier BV
Subject
Nutrition and Dietetics,General Medicine,Food Science
Reference29 articles.
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3. Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis;Belmont;BMC Pediatr,2002
4. Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency;Treem;Gastroenterology,1993
5. Clinical aspects and treatment of congenital sucrase-isomaltase deficiency;Treem;J Pediatr Gastroenterol Nutr,2012
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2. Congenital Sucrase–Isomaltase Deficiency: Same Mutation with Different Clinical Presentations;Turkish Journal of Gastroenterology;2024-04-01
3. Congenital sucrase–isomaltase deficiency in Türkiye; a single center experience;Scandinavian Journal of Gastroenterology;2024-03-08
4. Sucrase-Isomaltase Deficiency: Hiding in Plain Sight?;Current Treatment Options in Gastroenterology;2021-07-13
5. The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency;Quality of Life Research;2021-03-27
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