Zobrazeno 1 - 10
of 10
pro vyhledávání: '"E P Golitsina"'
Autor:
I G Rekhtina, E P Golitsina, E Iu Varlamova, V A Varshavskiĭ, A A Kireeva, L S Biriukova, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 85, Iss 3, Pp 80-85 (2013)
AIM: To study the pathomorphology of kidneys in patients with multiple myeloma (MM) and severe renal failure (RF) and to compare the results of morphological, immunohistochemical, and electron microscopic examinations of nephrobiopsy specimens with t
Externí odkaz:
https://doaj.org/article/40cd2255520d427f91dfb01fc676e1d1
Autor:
Irina Germanovna Rekhtina, Ekaterina Petrovna Golitsina, Lyudmila Semenovna Biryukova, I G Rekhtina, E P Golitsina, L S Biryukova
Publikováno v:
Терапевтический архив, Vol 83, Iss 7, Pp 65-68 (2011)
A rare variant of nephropathy in multiple myeloma (MM) is reported. Nephropathy is characterized basing on the study of nephrobiopsy with light, immunofluorescent and electron microscopy. A repeat biopsy of the kidney was made after achievement of a
Externí odkaz:
https://doaj.org/article/047cf285758a47c2b180a9e83f8515d5
Autor:
Svetlana Vladimirovna Gorchakova, Irina Germanovna Rekhtina, Konstantin Vladimirovich Yatskov, Galina Aleksandrovna Sukhanova, Ekaterina Petrovna Golitsina, Vladimir Anatol'evich Varshavskiy, Lyudmila Semenovna Biryukova, S V Gorchakova, I G Rekhtina, K V Yatskov, G A Sukhanova, E P Golitsina, V A Varshavsky, L S Biryukova
Publikováno v:
Терапевтический архив, Vol 81, Iss 7, Pp 78-82 (2009)
A case of the immunoglobuline deposit disease diagnosis in MM patient having the symptoms of intensive proteinuria, macrohematuria and terminal renal failure is reported. The disease was diagnosed by the evidence from electron microscopy of the kidne
Externí odkaz:
https://doaj.org/article/9efeb218e8d044bab1fd5eea1acd0cef
Autor:
I M Kutyrina, S A Martynov, M Yu Shvetsov, N L Livshits, N G Miroshnichenko, E P Golitsina, V A Varshavsky
Publikováno v:
Терапевтический архив, Vol 79, Iss 9, Pp 10-15 (2004)
Aim. To study prevalence of arterial hypertension (AH) in patients with chronic glomerulonephritis (CGN), its relationship with activity of the renal process, renal function; to analyse policy and efficacy of antihypertensive therapy. Material and me
Externí odkaz:
https://doaj.org/article/8d2865340ced4dbba056ff17d5a3c68b
Publikováno v:
Arkhiv patologii. 75(3)
Fibrillary glomerulonephritis is a disease from a group of glomerular diseases with organized deposits. Its etiology and pathogenesis have not been studied. The paper deals with the clinical, morphological, immunohistochemical, and electron microscop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5130a5af55ddd6bf04df56dd76fe67b4
https://pubmed.ncbi.nlm.nih.gov/24006767
https://pubmed.ncbi.nlm.nih.gov/24006767
Publikováno v:
Arkhiv patologii. 71(1)
Immunotactoid glomerulonephritis is a rare disease of unclear etiology and pathogenesis. Clinically immunotactoid glomerulonephritis manifests itself as the nephrotic syndrome in most cases. The diagnosis of the disease is based on electron microscop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d84cdbb12e9300b34ff2d256b6bda0e
https://pubmed.ncbi.nlm.nih.gov/19514359
https://pubmed.ncbi.nlm.nih.gov/19514359
Publikováno v:
Klinicheskaia meditsina. 87(3)
Amyloidosis is a pathology caused by tissue deposition of amyloid, a compound composed of insoluble fibrillar proteins. AL-amyloidosis (primary amyloidosis) most frequently leads to cardiac disorders 50% of which are cases of chronic heart failure (C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bf837b11289600a9806cefd7f61099a
https://pubmed.ncbi.nlm.nih.gov/19469251
https://pubmed.ncbi.nlm.nih.gov/19469251
Publikováno v:
Arkhiv patologii. 66(6)
The results of this study confirm the importance of virus infection in nephropathy onset and progression. Virus-like inclusions were found at electron microscopy in 70 (46 children and 24 adults) of 136 total diagnostic biopsies. In another group of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dabc548e81a5ab30f6cc6a4dfcf3fc39
https://pubmed.ncbi.nlm.nih.gov/15648164
https://pubmed.ncbi.nlm.nih.gov/15648164
Autor:
N A, Mukhin, L V, Kozlovskaia, I N, Bobkova, V V, Rameev, N B, Chebotareva, O K, Plieva, A V, Shcherbak, V A, Varshavskiĭ, E P, Golitsina
Publikováno v:
Arkhiv patologii. 66(6)
Tubulointerstitial fibrosis (TIF) is thought now to be a key factor in progression of renal failure in chronic nephropathies. A similar pattern of changes in glomerulonephritis and amyloidosis suggests common mechanisms operating in progression of re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4d256881f7c565f2f1e862ad67c9788
https://pubmed.ncbi.nlm.nih.gov/15648161
https://pubmed.ncbi.nlm.nih.gov/15648161
Autor:
I M, Kutyrina, S A, Martynov, M Iu, Shvetsov, N L, Lifshits, N G, Miroshnichenko, E P, Golitsina, V A, Varshavskiĭ
Publikováno v:
Terapevticheskii arkhiv. 76(9)
To study prevalence of arterial hypertension (AH) in patients with chronic glomerulonephritis (CGN), its relationship with activity of the renal process, renal function; to analyse policy and efficacy of antihypertensive therapy. MATERIAL AND METHODS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9585a812e2975c6d698293012ea6eab
https://pubmed.ncbi.nlm.nih.gov/15532369
https://pubmed.ncbi.nlm.nih.gov/15532369