Results 31 to 40 of about 544 (156)
A felnőttkori hypolactasia születésikohorsz-vizsgálata [PDF]
Abstract: Introduction and aim: To assess the prevalence of lactase gene promoter C/T13910 phenotypes in patients with lactose intolerance symptoms and to analyze the birth-cohort phenomenon in lactose-intolerant patients. Method: 1266 patients consulted between 2010 and 2017 were enrolled.
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DIGESTIVE DISORDERS IN PREMATURELY BORN CHILDREN
The article contains data on functional digestive disorders in newborns, mainly on the problem of lactase (disaccharidase) insufficiency. The information on the prevalence of this condition, modern classification of hypolactasia, diagnostic techniques ...
I. A. Belyaeva +2 more
doaj +1 more source
Lactase (LCT) deficiency affects approximately 75% of the world's adult population and may lead to lactose malabsorption and intolerance. Currently, the regulation of LCT gene expression remains poorly known.
Mathurin Fumery +13 more
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Lactose Hydrolysis in Milk and Dairy Whey Using Microbial β‐Galactosidases
This work aimed at evaluating the influence of enzyme concentration, temperature, and reaction time in the lactose hydrolysis process in milk, cheese whey, and whey permeate, using two commercial β‐galactosidases of microbial origins. We used Aspergillus oryzae (at temperatures of 10 and 55°C) and Kluyveromyces lactis (at temperatures of 10 and 37°C) β‐
Michele Dutra Rosolen +4 more
wiley +1 more source
Review article: Evidence‐based dietary management of inflammatory bowel disease
Summary Background Dietary management of patients with inflammatory bowel disease (IBD) involves more than defining a therapeutic diet. The profusion of ‘expert advice’ is not necessarily built on evidence. Aims To provide evidence‐based guidance on all clinically relevant aspects of nutritional and dietary management of patients with IBD.
Peter R. Gibson +2 more
wiley +1 more source
The aim of this study was to establish a retrospective evaluation and comparison of the hydrogen/methane (H2/CH4) breath test and genetic test (C/T−13910 polymorphism) results in lactose malabsorption testing. In total 263 consecutive patients with suspected lactose malabsorption were included in this study.
Dietmar Enko +4 more
wiley +1 more source
Objective. To establish whether supplementation with a standard oral dose of Beta‐Galactosidase affects hydrogen breath excretion in patients presenting with lactose malabsorption. Methods. Ninety‐six consecutive patients positive to H2 Lactose Breath Test were enrolled.
Ivan Ibba +4 more
wiley +1 more source
Hypolactasia associated with severe iron-deficiency anemia has been reported in several studies. The objective of the present study was to determine whether hypolactasia is associated with the degree and duration of iron-deficiency anemia.
M.R. Vieira +2 more
doaj +1 more source
Adult-type hypolactasia and lactose malabsorption in Poland.
The available data on the incidence of lactose malabsorption are contradictory. Potential bias in random selection is a major drawback of studies performed to-date. Moreover, molecular analysis of polymorphism -13910 C>T upstream of the lactase (LCT) gene (NM_005915.4:c.1917+326C>T; rs4988235) has not been reported in those studies. Therefore, in
Mądry, E. +7 more
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Regulation of intestinal lactase in adult hypolactasia. [PDF]
Relative deficiency of intestinal lactase activity during adulthood, adult hypolactasia, is a common condition worldwide. We studied the regulation of lactase-phlorizin hydrolase in normal and adult hypolactasic subjects by correlating transcript abundance in intestinal biopsies with relative synthetic rates for the protein in cultured intestinal ...
M, Lloyd +8 more
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