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Literature DB >> 23103658

Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.

William R Treem¹.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 2012 PMID： 23103658 DOI： 10.1097/01.mpg.0000421401.57633.90

Source DB: PubMed Journal: J Pediatr Gastroenterol Nutr ISSN： 0277-2116 Impact factor: 2.839

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23 in total

1. Variable Use of Disaccharidase Assays When Evaluating Abdominal Pain.

Authors: Stanley A Cohen; Hannah Oloyede
Journal: Gastroenterol Hepatol (N Y) Date: 2018-01

2. Structure-function analysis of human sucrase-isomaltase identifies key residues required for catalytic activity.

Authors: Birthe Gericke; Natalie Schecker; Mahdi Amiri; Hassan Y Naim
Journal: J Biol Chem Date: 2017-05-18 Impact factor: 5.157

3. Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

Authors: Julien L Marcadier; Margaret Boland; C Ronald Scott; Kheirie Issa; Zaining Wu; Adam D McIntyre; Robert A Hegele; Michael T Geraghty; Matthew A Lines
Journal: CMAJ Date: 2014-12-01 Impact factor: 8.262

4. The Role of Metal Oxide Nanoparticles, Escherichia coli, and Lactobacillus rhamnosus on Small Intestinal Enzyme Activity.

Authors: Alba García-Rodríguez; Fabiola Moreno-Olivas; Ricard Marcos; Elad Tako; Cláudia N H Marques; Gretchen J Mahler
Journal: Environ Sci Nano Date: 2020-11-09

5. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

Authors: Ozge Ceyhan-Birsoy; Jaclyn B Murry; Kalotina Machini; Matthew S Lebo; Timothy W Yu; Shawn Fayer; Casie A Genetti; Talia S Schwartz; Pankaj B Agrawal; Richard B Parad; Ingrid A Holm; Amy L McGuire; Robert C Green; Heidi L Rehm; Alan H Beggs
Journal: Am J Hum Genet Date: 2019-01-03 Impact factor: 11.025

Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.

1. Variable Use of Disaccharidase Assays When Evaluating Abdominal Pain.

2. Structure-function analysis of human sucrase-isomaltase identifies key residues required for catalytic activity.

3. Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

4. The Role of Metal Oxide Nanoparticles, Escherichia coli, and Lactobacillus rhamnosus on Small Intestinal Enzyme Activity.

5. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

6. Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.

Review 7. What Are the Pearls and Pitfalls of the Dietary Management for Chronic Diarrhoea?

8. The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.

Review 9. Routine disaccharidase testing: are we there yet?

10. Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.