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Literature DB >> 4952790

Sugar malabsorption due to deficiencies of disaccharidase activities and of monosaccharide transport.

A Holzel.

Abstract

Entities: Chemical Disease

Mesh：

Substances：

Year: 1967 PMID： 4952790 PMCID： PMC2019782 DOI： 10.1136/adc.42.224.341

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

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62 in total

1. SODIUM ACTIVATION OF HUMAN INTESTINAL SUCRASE AND ITS POSSIBLE SIGNIFICANCE IN THE ENZYME ORGANIZATION OF BRUSH BORDERS.

Authors: G SEMENZA; R TOSI; M C VALLOTTON-DELACHAUX; E MUELHAUPT
Journal: Biochim Biophys Acta Date: 1964-07-08

2. Intestinal sucrase and isomaltase deficiency in two siblings.

Authors: C M ANDERSON; M MESSER; R R TOWNLEY; M FREEMAN
Journal: Pediatrics Date: 1963-06 Impact factor: 7.124

3. INTESTINAL ABSORPTION OF SUCROSE IN MAN: THE SITE OF HYDROLYSIS AND ABSORPTION.

Authors: G M GRAY; F J INGELFINGER
Journal: J Clin Invest Date: 1965-03 Impact factor: 14.808

4. A defect in disaccharide metabolism after gastrojejunostomy.

Authors: J D GRYBOSKI; W R THAYER; W A GRYBOSKI; I W GABRIELSON; H M SPIRO
Journal: N Engl J Med Date: 1963-01-10 Impact factor: 91.245

5. Severe lactose intolerance in infancy.

Authors: A HOLZEL; T MEREU; M L THOMSON
Journal: Lancet Date: 1962-12-29 Impact factor: 79.321

6. Tribal incidence of lactase deficiency in Uganda.

Authors: G C Cook; S K Kajubi
Journal: Lancet Date: 1966-04-02 Impact factor: 79.321

7. Intestinal lactase deficiency and lactose intolerance in adults.

Authors: F Kern; J E Struthers
Journal: JAMA Date: 1966-03-14 Impact factor: 56.272

8. [On the residual activity of defective enzymes in hereditary monosaccharide and disaccharide malabsorption].

Authors: F Linneweh; E Schaumlöffel; E H Graul; H H Bode
Journal: Schweiz Med Wochenschr Date: 1966-04-02

9. [Lactate deficiency of the mucosa of the small intestine as the cause of certain forms of acquired milk intolerance in adults].

Authors: U P Haemmerli; H J Kistler; R Ammann; S Auricchio; A Prader
Journal: Helv Med Acta Date: 1963-11

10. Postnatal changes in beta-galactosidase activity in the jejunum and ileum of mice, rabbits, and guinea pigs.

Authors: O Koldovský; A Heringová; V Jirsová; F Chytil; J Hosková
Journal: Can J Biochem Date: 1966-05

15 in total

Review 1. Sugar-induced diarrhoea in children.

Authors: M Gracey; V Burke
Journal: Arch Dis Child Date: 1973-05 Impact factor: 3.791

Sugar malabsorption due to deficiencies of disaccharidase activities and of monosaccharide transport.

1. SODIUM ACTIVATION OF HUMAN INTESTINAL SUCRASE AND ITS POSSIBLE SIGNIFICANCE IN THE ENZYME ORGANIZATION OF BRUSH BORDERS.

2. Intestinal sucrase and isomaltase deficiency in two siblings.

3. INTESTINAL ABSORPTION OF SUCROSE IN MAN: THE SITE OF HYDROLYSIS AND ABSORPTION.

4. A defect in disaccharide metabolism after gastrojejunostomy.

5. Severe lactose intolerance in infancy.

6. Tribal incidence of lactase deficiency in Uganda.

7. Intestinal lactase deficiency and lactose intolerance in adults.

8. [On the residual activity of defective enzymes in hereditary monosaccharide and disaccharide malabsorption].

9. [Lactate deficiency of the mucosa of the small intestine as the cause of certain forms of acquired milk intolerance in adults].

10. Postnatal changes in beta-galactosidase activity in the jejunum and ileum of mice, rabbits, and guinea pigs.

Review 1. Sugar-induced diarrhoea in children.

2. Editorial: sugar-induced diarrhea in children.

3. Role of chemical examination of the stool in diagnosis of sugar malabsorption in children.

4. Comparison of three methods used in assessment of carbohydrate absorption in malnourished children.

Review 5. The management of chronic or recurrent diarrhoea in childhood.

6. [Small intestine suction biopsy in childhood: technic complications, importance in diagnosis of intestinal diseases].

7. Tolerance of young children with severe gastroenteritis to dietary lactose: a controlled study.

8. Congenital lactose malabsorption.

9. Persistent post-enteritis diarrhoea.

10. Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).