Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D. V. Svetlichnaya"'
Autor:
E. A. Kulish, A. S. Kotov, E. V. Mukhina, Y. Y. Kotalevskaya, D. V. Svetlichnaya, M. V. Panteleeva
Publikováno v:
Русский журнал детской неврологии, Vol 14, Iss 2, Pp 23-28 (2019)
The authors present a unique clinical observation of the case of a hereditary deficiency of a type 1 glucose transporter, also called de Vivo disease. The type 1 glucose transporter deficiency syndrome (OMIM: 606777, ORPHA: 71277) is an extremely rar
Externí odkaz:
https://doaj.org/article/2f29544abdc54bd7bfb1533877c69f48
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9893130bce3b4d4a377efff09f6b8f0a
https://doi.org/10.18565/urology.2020.6.126-130
https://doi.org/10.18565/urology.2020.6.126-130
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40c0d9da16181f440e807e92a414e05
https://doi.org/10.18565/urology.2020.3.81-86
https://doi.org/10.18565/urology.2020.3.81-86
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1abe91cffbb58c79bb7c3ac7820fd17
https://doi.org/10.18565/urology.2019.6.125-130
https://doi.org/10.18565/urology.2019.6.125-130
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2db88ec79ffb72e0868632aaa49736f
https://doi.org/10.18565/urology.2019.5.140-143
https://doi.org/10.18565/urology.2019.5.140-143
Autor:
M M, Litvinova, T V, Filippova, K F, Khafizov, D V, Svetlichnaya, D A, Ahmedzyanova, V I, Rudenko, Z K, Gadzhieva, M V, Shumikhina
Publikováno v:
Urologiia (Moscow, Russia : 1999). (6)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11278933bd1ecefdbf51fb19a1304754
https://pubmed.ncbi.nlm.nih.gov/33377691
https://pubmed.ncbi.nlm.nih.gov/33377691
Autor:
T V Filippova, Sevda Z Nuralieva, Lilit Egshatyan, D V Svetlichnaya, Aliy Yu. Asanov, M M Litvinova
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1de17aadf60048fb135016b75d8fb1ab
https://doi.org/10.1530/endoabs.70.aep185
https://doi.org/10.1530/endoabs.70.aep185
Autor:
T V, Filippova, D V, Svetlichnaya, V I, Rudenko, Y G, Alyaev, E G, Tadevosyan, M M, Azova, T I, Subbotina, Z K, Gadzhieva, A Y, Asanov, K R, Khamidullin, A M, Pushkarev, M M, Litvinova
Publikováno v:
Urologiia (Moscow, Russia : 1999). (6)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abe8ed86cd176295bec14271ea9839eb
https://pubmed.ncbi.nlm.nih.gov/32003182
https://pubmed.ncbi.nlm.nih.gov/32003182
Autor:
T V, Filippova, D V, Svetlichnaya, V I, Rudenko, Y G, Alyaev, M V, Shumikhina, M M, Azova, T I, Subbotina, Z K, Gadzhieva, A Yu, Asanov, M M, Litvinova
Publikováno v:
Urologiia (Moscow, Russia : 1999). (5)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88c5cf3a4ef4948b6b2c60e194c56b09
https://pubmed.ncbi.nlm.nih.gov/31808650
https://pubmed.ncbi.nlm.nih.gov/31808650