Results 41 to 50 of about 713 (175)
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
Lactose in drugs and lactose intolerance – realities and myths
Lactose intolerance is a set of clinical symptoms occurring after lactose intake, characterised by abdominal pain, bloating and diarrhoea. Adult-type hypolactasia is the most common cause of lactose intolerance and is associated with the physiological ...
Zygmunt Zdrojewicz +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
doaj +1 more source
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
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
Molecular genetics of adult‐type hypolactasia
Adult-type hypolactasia (lactase non-persistence; primary lactose malabsorption) is characterized by the down-regulation of the lactase enzyme activity in the intestinal wall after weaning. The down-regulation is genetically determined and a mutation has occurred that has made part of mankind tolerate milk (lactase persistence).
openaire +2 more sources
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
Nezgoda I., Naumenko O. Rotavirus infection in children with different variants allelic polymorphism C> T 13910 gene LCT = Перебіг ротавірусної інфекції у дітей з різними варіантами алельного поліморфізму С >Т 13910 гена лактази.
I. Nezgoda, O. Naumenko
doaj +3 more sources

