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Atheroembolic renal disease and membranous nephropathy, in a patient with myelodysplastic syndrome, eosinophilia, and trisomy 8

Autor: Dimitra Rontoianni, Sotsiou F, John Apostolidis, T. Apostolou, Constantinos Pappas, Nikoletta Nikolopoulou

Publikováno v: Nephrology Dialysis Transplantation. 17:1336-1338

Atheroembolic renal disease (ARD) is an important and often misdiagnosed cause of renal failure. It usually occurs in adult patients suffering from atherosclerosis and is a result of embolization of cholesterol crystals from atheromatous plaques, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::953797d5cb45fdec66289be64c9f937f
https://doi.org/10.1093/ndt/17.7.1336

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Skin Biopsy for the diagnosis of Alport Syndrome

Autor: Lagona, E, Tsartsali, L, Kostaridou, S, Skiathitou, A, Georgaki, E, Sotsiou, F

Alport syndrome (AS) is the most common hereditary nephritis often associated with extrarenal manifestations. It was first described by Alport on 1927. There is a primary disorder in collagen type IV which is the main component of the basement membra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cf9968f0acb72eb7408a87775390a325
https://europepmc.org/articles/PMC2464308/

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Reduction in glucocorticoid receptors in renal biopsies of patients with lupus nephritis

Autor: Sotsiou F, Nikoletta Nikolopoulou, Anna A. Tziraki, Michael A. Tzirakis, Paraskevi Moutsatsou, Valsamakis Hadjiconstantinou, Antonios Kominakis

Publikováno v: Clinical biochemistry. 40(16-17)

Objectives: The first-line treatment for lupus nephritis is the administration of glucocorticoids (GC) that mediate their effects via the glucocorticoid receptor (GR). The aim of this study was to investigate the expression of GR protein in the corti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64e98cd6ec4fbc0591a24437067392d
https://pubmed.ncbi.nlm.nih.gov/17880936

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Antiphospholipid syndrome nephropathy in patients with systemic lupus erythematosus and antiphospholipid antibodies: Prevalence, clinical associations, and long-term outcome

Autor: Tektonidou, M.G. Sotsiou, F. Nakopoulou, L. Vlachoyiannopoulos, P.G. Moutsopoulos, H.M.

Objective. To evaluate the prevalence, clinical associations, and outcome of antiphospholipid syndrome (APS) nephropathy in patients with systemic lupus erythematosus (SLE) and antiphospholipid antibodies (aPL) and in SLE patients without aPL. Method

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::74ed224bdd9f8f0c2b2e51e704c84827
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3004746

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Clinicopathologic predictors of death and ESRD in patients with pauci-immune necrotizing glomerulonephritis

Autor: Kapitsinou, P. P., Ioannidis, J. P., Boletis, J. N., Sotsiou, F., Nakopoulou, L., Daphnis, E., Moutsopoulos, H. M.

BACKGROUND: Pauci-immune necrotizing glomerulonephritis (PING) occurs in various settings and has a very variable prognosis. We investigated whether clinicopathologic findings at the time of renal biopsy may predict major disease outcomes. METHODS: W

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10561::759ce38a4a2fb9747724661a51e01510
http://olympias.lib.uoi.gr/jspui/handle/123456789/23047

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Clinicopathologic predictors of death and ESRD in patients with pauci-immune necrotizing glomerulonephritis

Autor: Kapitsinou, PP Ioannidis, JPA Boletis, JN Sotsiou, F and Nakopoulou, L Daphnis, E Moutsopoulos, HM

Background: Pauci-immune necrotizing glomerulonephritis (PING) occurs in various settings and has a very variable prognosis. We investigated whether clinicopathologic findings at the time of renal biopsy may predict major disease outcomes. Methods: W

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::7d8d5b1458ea53fffdcacd4de8cc24cd
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082797

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