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Hypoxia-Inducible Factor-1α (HIF-1α) expression is upregulated in Sickle Cell Disease (SCD) and correlates with various laboratory markers of disease severity. Nitric Oxide plays a pivotal role in SCD pathophysiology and endothelial Nitric Oxide Sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::39ea766e6b0638f239bcdaf49523100e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077108
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077108
Sickle cell disease (SCD), a hereditary form of chronic hemolytic anemia, is characterized by acute vascular occlusion and chronic complications as pulmonary hypertension (PH), a hallmark of higher mortality. This study aimed to determine peripheral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a48925dfca51130f583101423260e65a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3122186
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3122186
In this article, we present data on endothelial Nitric Oxide Synthase (eNOS) gene T786C and G894T polymorphisms in Greek steady-state Sickle Cell Disease patients in comparison to healthy controls. Moreover, eNOS mRNA levels were determined in periph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6b7439de8588662f9e339257b5178f2f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056724
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056724
Endothelial Nitric Oxide Synthase (eNOS) is crucial for vascular homeostasis. Polymorphisms T786C and G894T affect eNOS regulation and have been related to various diseases. Sickle Cell Disease (SCD), a clinically diverse chronic hemolytic anemia, im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::845f7f3a8b89fd022b6798e23c20fb89
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086755
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086755
Splenomegaly is a common finding in beta-thalassemia; however, its hemodynamic features and its potential correlations with high output state and hepatic disorders, both also frequent in thalassemia, have not yet been assessed in these patients. Eigh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6e1b0c83df613e8af6a373c4eb134172
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3092579
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3092579
Multiple myeloma (MM) is rare among patients with sickle cell syndromes (SCS). We describe six Greek sickle cell patients aged 56 to 65 years: five haemoglobin S beta (+)thalassaemia (HbS beta (+)thal), one sickle cell anaemia (HbSS), who developed M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::2ca5da90cb5ad386e9e357c368b49ccc
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3054387
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3054387
Behcet’s disease (BD) is a chronic, relapsing vasculitis of unknown etiology. Its association with chronic myelogenous leukemia (CML) is extremely rare, and typical manifestations of an were observed in a very few patients with CML, mainly under in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a92db4ed975adf0f5497a1488a9e4766
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3054252
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3054252
Publikováno v:
Transplantation. 65(10)
Background. Neurotoxicity is a well-recognized side effect of cyclosporine therapy in transplant recipients. Cyclosporine can cause a wide range of adverse effects on both the central and peripheral nervous systems. Methods. We present a case history
Publikováno v:
Thrombosis et diathesis haemorrhagica. 1(2)