Results 21 to 30 of about 896,464 (230)

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD) [PDF]

BMC Gastroenterology, 2009
Background Congenital lactase deficiency (CLD) is a severe gastrointestinal disorder of newborns. The diagnosis is challenging and based on clinical symptoms and low lactase activity in intestinal biopsy specimens.
Höglund Pia, Catassi Carlo, Gijsbers Carolien, Routi Taina, Freddara Roberta, Torniainen Suvi, Savilahti Erkki, Järvelä Irma   +7 more
doaj   +2 more sources

Lactase Deficiency [PDF]

Nature, 1969
Michael A. Crawford
  +6 more sources

Клінічні форми лактазної недостатності в дітей

Gastroenterologìa, 2018
Актуальність. Лактазна недостатність (ЛН) — найбільш часта патологія тонкої кишки, для якої характерний розвиток синдрому порушеного травлення і всмоктування, пов’язаного з відсутністю або недостатньою активністю ферменту лактази.
T.V. Sorokman, N.A. Popelyuk, L.V. Shvygar   +2 more
doaj   +2 more sources

Lactase deficiency in children

Zdorovʹe Rebenka, 2012
In this paper the etiological, pathogenetic, clinical, laboratory and instrumental characteristic of lactase deficiency in children are presented. The features of feeding/nutrition, treatment of children with this disease are described.
N.V. Nagorna, Ye.V. Bordyugova, G.V. Dubova   +2 more
doaj   +2 more sources

Sishen Pill treats spleen-kidney yang deficiency IBS-D by influencing ATPase activity and intestinal microbiota [PDF]

Frontiers in Microbiology
BackgroundSishen Pill (SSP) has therapeutic effects on spleen-kidney yang deficiency diarrhea-predominant irritable bowel syndrome (IBS-D). Studies have shown that IBS-D with spleen-kidney yang deficiency is characterized by intestinal microbiota ...
Qi Long, Qi Long, Liwen Li, Liwen Li, Zhoujin Tan, Zhoujin Tan, Na Deng, Na Deng   +7 more
doaj   +2 more sources

CLINICAL AND BIOCHEMICAL ASPECTS OF SECONDARY LACTASE DEFICIENCY IN YOUNG CHILDREN

ОБРАЗОВАНИЕ НАУКА И ИННОВАЦИОННЫЕ ИДЕИ В МИРЕ
: Secondary lactase deficiency (SLD) is one of the common causes of malabsorption syndrome in young children and often develops against the background of acute and chronic diseases of the gastrointestinal tract.
Ahmadaliyev Sh.Sh., Askarova Feruza Gairatjon qizi   +1 more
semanticscholar   +3 more sources

[Genetics of lactase deficiency in Russia].

Voprosy pitaniia
The ability to digest lactose in adulthood is caused by a genetic mutation that emerged following the domestication of cattle approximately 10 000 years ago.
E. Kovalenko, E. Vergasova, O. Shoshina, M.S. Sheludchenko, Iaroslav Popov, A. Kim, N. Plotnikov, A. Rakitko, O.I. Volokh   +8 more
semanticscholar   +3 more sources

Dietotherapy in children with obesity associated with adult lactase deficiency

Zdorovʹe Rebenka, 2017
Background. Excess lactose in the infant’s nutrition, especially in combination with adult lactase deficiency (С/C 13910 genotype), promotes the persistence of a chronic inflammatory process associated with the formation of obesity-complicated insulin ...
A.E. Abaturov, A.A. Nikulina, D.V. Logvinov, P.A. Kolbasin   +3 more
doaj   +2 more sources

Lactase Deficiency in Children With Cystic Fibrosis

Педиатрическая фармакология, 2017
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Irina G. Gordeeva
doaj   +3 more sources

Primary Lactase Deficiency: Genetic or Acquired?

Gastroenterology, 1970
From a critical review of the literature, it would appear that, in animals, intestinal lactase is an adaptive enzyme, with adaptation occurring in 5–8 weeks. In man, short-term attempts at adaptation have not been successful, although a fall in lactase activity or lactose absorption has been found after substrate withdrawal in some subjects.
T D, Bolin, A E, Davis
openaire   +4 more sources