Publications by authors named "Y M Vakhrushev"

Aim: To characterize of the features of changes in the cavity and parietal microbiota of the small intestine in patients with non-alcoholic fatty liver disease (NAFLD).

Materials And Methods: Fifty four patients with NAFLD at the stage of steatosis and steatohepatitis at the age of 1860 years were examined. The diagnosis was verified by ultrasound of the hepatobiliary system using a SONIX OP analyzer (Canada), FibroMax test data and liver elastography using an AIXPLORER apparatus (France).

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Aim: To assess the psychoemotional status and the state of the autonomic nervous system and their importance in the violation of the motor-evacuation function of the gastrointestinal tract in chronic duodenal insufficiency (CDI).

Materials And Methods: A prospective study of 40 patients with CDI was carried out. The control group consisted of 30 healthy individuals.

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Aim: A comprehensive assessment of metabolic parameters in patients with non-alcoholic fatty liver disease and based on them the development of prognostic criteria for the development of liver fibrosis.

Materials And Methods: 288 patients with non-alcoholic fatty liver disease at the stage of steatosis were examined. The patients underwent ultrasound examination of the hepatobiliary system using the SONIX OP apparatus (Canada), the FibroMax test, and liver elastography using the AIXPLORER apparatus (France).

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Aim: To study the basic metabolic functions of the liver in patients with non-alcoholic fatty liver disease and to assess the relationship of these disorders with the bacterial overgrowth syndrome.

Materials And Methods: 50 patients with non-alcoholic fatty liver disease at the stage of steatosis were examined. In the verification of the diagnosis, hepatobiliary system ultrasound and FibroMax test data were used.

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Article Synopsis
  • RNA-binding motif protein 20 (RBM20) is crucial for splicing various cardiac genes, and mutations in this protein can lead to serious heart diseases like cardiomyopathies.
  • The initial discovery linked RBM20 mutations to dilated cardiomyopathy through improper splicing of the titin gene, which is vital for heart muscle function.
  • This summary also highlights a specific clinical case of an uncommon arrhythmogenic phenotype related to an unclear genetic variant, despite the absence of visible heart structure issues.
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