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Page 1
Food Intolerances.
Tuck CJ, Biesiekierski JR, Schmid-Grendelmeier P, Pohl D. Tuck CJ, et al. Nutrients. 2019 Jul 22;11(7):1684. doi: 10.3390/nu11071684. Nutrients. 2019. PMID: 31336652 Free PMC article. Review.
Enzyme deficiencies have been proposed to result in other food sensitivities including low amine oxidase activity resulting in histamine intolerance and sucrase-isomaltase deficiency resulting in reduced tolerance to sugars and starch. ...
Enzyme deficiencies have been proposed to result in other food sensitivities including low amine oxidase activity resulting in histamine int …
Genetic and acquired sucrase-isomaltase deficiency: A clinical review.
Danialifar TF, Chumpitazi BP, Mehta DI, Di Lorenzo C. Danialifar TF, et al. J Pediatr Gastroenterol Nutr. 2024 Apr;78(4):774-782. doi: 10.1002/jpn3.12151. Epub 2024 Feb 8. J Pediatr Gastroenterol Nutr. 2024. PMID: 38327254 Review.
Genetic sucrase-isomaltase deficiency (GSID) is an inherited deficiency in the ability to digest sucrose and potentially starch due to mutations in the sucrase-isomaltase (SI) gene. Congenital sucrase-isomaltase deficiency is historically …
Genetic sucrase-isomaltase deficiency (GSID) is an inherited deficiency in the ability to digest sucrose and potentiall …
Congenital sucrase-isomaltase deficiency.
Treem WR. Treem WR. J Pediatr Gastroenterol Nutr. 1995 Jul;21(1):1-14. doi: 10.1097/00005176-199507000-00001. J Pediatr Gastroenterol Nutr. 1995. PMID: 8576798 Review. No abstract available.
The History of Maltose-active Disaccharidases.
Lentze MJ. Lentze MJ. J Pediatr Gastroenterol Nutr. 2018 Jun;66 Suppl 3:S4-S6. doi: 10.1097/MPG.0000000000001960. J Pediatr Gastroenterol Nutr. 2018. PMID: 29762367 Review.
Borkstrom's coworker, Dahlqvist, investigated the maltose-active enzymes in pig intestine, and a second group around Semenza studied the maltase-active enzymes in rabbit intestine. After the first descriptions of congenital sucrase-isomaltase deficiency in 19 …
Borkstrom's coworker, Dahlqvist, investigated the maltose-active enzymes in pig intestine, and a second group around Semenza studied the mal …
Selected disorders of malabsorption.
Siddiqui Z, Osayande AS. Siddiqui Z, et al. Prim Care. 2011 Sep;38(3):395-414; vii. doi: 10.1016/j.pop.2011.05.002. Prim Care. 2011. PMID: 21872088 Review.
These disorders may be congenital or acquired and include cystic fibrosis and Shwachman-Diamond syndrome; the rare congenital lactase deficiency; glucose-galactose malabsorption; sucrase-isomaltase deficiency; adult-type hypolactasia leading to acquired lacto …
These disorders may be congenital or acquired and include cystic fibrosis and Shwachman-Diamond syndrome; the rare congenital lactase defici …
Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
Wanes D, Husein DM, Naim HY. Wanes D, et al. Nutrients. 2019 Feb 22;11(2):461. doi: 10.3390/nu11020461. Nutrients. 2019. PMID: 30813293 Free PMC article. Review.
The symptoms are similar to those in other carbohydrate malabsorption disorders, such as congenital sucrase-isomaltase deficiency, and include severe osmotic watery diarrhea. ...
The symptoms are similar to those in other carbohydrate malabsorption disorders, such as congenital sucrase-isomaltase defi …
Disaccharide digestion and maldigestion.
Gudmand-Høyer E, Skovbjerg H. Gudmand-Høyer E, et al. Scand J Gastroenterol Suppl. 1996;216:111-21. doi: 10.3109/00365529609094566. Scand J Gastroenterol Suppl. 1996. PMID: 8726284 Review.
However, the prevalence varies widely between different populations. Sucrase-isomaltase deficiency is a very rare congenital condition except in Greenland. ...
However, the prevalence varies widely between different populations. Sucrase-isomaltase deficiency is a very rare conge …
18 results