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Objective To explore the frequency and impact of an autoimmune disease past-medical history (PMH) in the clinical picture and outcomes of patients with antineutrophil cytoplasmic autoantibodies (ANCA) associated vasculitis (AAV). Methods This was a r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f3d10e885570d2270a063aa272120b85
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219551
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219551
Early diagnosis and initiation of appropriate immunosuppressive treatment remain the cornerstone of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis at the cost of significant toxicity. In this report, we present a case of a 69-year-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e9fa75beb7dab51c2dc70c94674f9166
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219308
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219308
Autor:
Kapsia, E. Marinaki, S. Michelakis, I. Liapis, G. Sfikakis, P.P. Tektonidou, M.G. Boletis, J.
Introduction: Pure membranous lupus nephritis (MLN) accounts for 10–20% of total cases of lupus nephritis and is generally associated with a better patient and renal survival compared to proliferative classes. Studies of MLN are limited by small sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a8d41affcb4c78a36f4862160013916c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219520
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219520
Objectives Kidney transplant (KTx) recipients with IgAN as primary disease, were compared with recipients with other causes of renal failure, in terms of long-term outcomes. Methods Ninety-nine KTx recipients with end-stage kidney disease (ESKD) due
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https://explore.openaire.eu/search/publication?articleId=od______2127::6b6544ee60b49d21bb198e5282784ce4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056270
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056270
Fibrillary glomerulonephritis (FGN) is a diverse glomerular disease with poor renal prognosis. The optimal therapeutic approach remains undetermined, as treatment outcomes vary across different studies.We retrospectively reviewed the medical data of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d690bc3ca81e465eafc5ef436e3f3d05
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102399
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102399
Background: Hypocomplementemic urticarial vasculitis syndrome is an infrequent condition characterized by ocular, renal, gastrointestinal and pulmonary involvement with low serum complement levels and autoantibodies. Renal manifestations vary from mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::211e4075305115798988ece61ccb1b4e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104019
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104019
Background: Nuchal-type fibroma is a rare benign tumor arising from the connective tissue. Our aim was to present our experience via two cases of this tumor and a comprehensive review of the literature. Patients and Methods: We report a case of a 23-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6958460a9c07ad9f569077ea47ea6b9b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020744
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020744
Kidney involvement is frequent in patients with systemic lupus erythematosus (SLE), although it may not be present from disease onset. Renal lupus itself is highly heterogenous with respect to the combination and/or severity of clinical and/or labora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::0a83a8ac80458b21fbe3932e536ab48f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104908
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104908
Autor:
Mylona, E., Alexandrou, P., Mpakali, A., Giannopoulou, I., Liapis, G., Markaki, S., Keramopoulos, A., Nakopoulou, L.
Publikováno v:
In European Journal of Surgical Oncology 2007 33(3):294-300