Zobrazeno 1 - 10
of 90
pro vyhledávání: '"V I Rudenko"'
Publikováno v:
Measurement Techniques. 65:679-685
Publikováno v:
Experimental and Сlinical Urology. 14:100-110
Introduction. Purine dysmetabolism is occured by increased production of uric acid, which leads to hyperuricemia and hyperuricuria. The most common forms of purine metabolism disorders are the uratenephropathy, gout, and asymptomatic hyperuricemia. P
Autor:
V I Rudenko, Yu L Demidko
Publikováno v:
Фармакология & Фармакотерапия. :54-59
Autor:
Kamil Khafizov, Z K Gadzhieva, D A Ahmedzyanova, M M Litvinova, T V Filippova, M V Shumikhina, V I Rudenko, D V Svetlichnaya
Publikováno v:
Urologiia. :126-130
The article describes a clinical case of kidney stone disease (KSD) in a child of 4 y.o. with calcium urolithiasis. Analysis of chemical content of the kidney stones revealed their calcium-oxalate composition. According to the results of clinical exo
Publikováno v:
Тонкие химические технологии, Vol 8, Iss 4, Pp 64-72 (2013)
For the first time the composition and microstructure of large (more than 2 cm) urinary stones, including staghorn stones, were studied according to their volume by a set of techniques (X-ray, X-ray microanalysis, scanning electron microscopy, infrar
Externí odkaz:
https://doaj.org/article/5d946404da5d4ae7ad7cb3111207c9f3
Autor:
M V Shumikhina, T I Subbotina, M M Litvinova, S Z Nuralieva, T V Filippova, D V Svetlichnaya, I S Chugunov, S L Morozov, Z K Gadzhieva, V I Rudenko
Publikováno v:
Scopus-Elsevier
Kidney stone disease (KSD) is an actual problem of modern health care. By now, more than 80 monogenic forms of urolithiasis have been described. To diagnose such forms of KSD different molecular genetic technologies are used. In the current article 5
Autor:
Yuri Alyaev, V I Rudenko, D V Svetlichnaya, M M Litvinova, T I Subbotina, Z K Gadzhieva, E G Tadevosyan, T V Filippova, A Y Asanov, K R Khamidullin, M M Azova, A M Pushkarev
Publikováno v:
Urologiia. :125-130
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease. The mutations in the AGXT, GRHPR, HOGA1 genes are
Autor:
K A Aleksandrova, T.I. Miskaryan, D.N. Fiev, V I Rudenko, L.B. Kapanadze, N S Serova, M A Gazimiev
Publikováno v:
Urologiia. :38-43
Introduction Urinary stone disease is one of the most significant urologic diseases, since its prevalence increases annually, which makes it necessary to study and improve effective preventive measures, diagnostic methods and to implement new treatme
Publikováno v:
Urologiia. :31-36
The aim To assess the diagnostic performance of dual-energy computed tomography (DECT) in the evaluation of the composition of urinary stones "in vivo". Materials and methods A total of 91 patients aged from 20 to 70 years old (mean 42.7) with urinar
Autor:
Yuri Alyaev, V I Rudenko, T I Subbotina, Z K Gadzhieva, D V Svetlichnaya, A Y Asanov, M V Shumikhina, M M Azova, T V Filippova, M M Litvinova
Publikováno v:
Urologiia. :140-143
Primary hyperoxaluria is a group of inherited metabolic diseases characterized by increased formation of calcium-oxalate stones in kidneys with development of nephrolithiasis and chronic kidney disease. The article summarizes the modern information o