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Risk factors for predicting venous thromboembolism in patients with nephrotic syndrome: focus on haemostasis-related parameters
PurposeThe venous thromboembolic events (VTE) incidence is high in nephrotic syndrome (NS). We aimed to assess prospectively the risk of VTE in a large cohort of NS patients and to identifyExpand
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Molecular adsorbents recirculating system in patients with severe liver failure. Experience of a single Romanian centre.
AIM This is a retrospective, observational study regarding the experience of the Fundeni Clinical Institute in the application of the Molecular Adsorbents Recirculating System in patients with liverExpand
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Validation study of Oxford Classification of IgA Nephropathy: the significance of extracapillary hypercellularity and mesangial IgG immunostaining
The Oxford classification (OC) of IgA Nephropathy (IgAN) identified mesangial hypercellularity (M), endocapillary hypercellularity (E), segmental glomerulosclerosis (S), and tubularExpand
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“Associated” or “Secondary” IgA nephropathy? An outcome analysis
Background Whether differences in outcome between primary (pIgAN) and secondary IgA nephropathy (sIgAN) exist is uncertain. Methods We conducted a retrospective, observational study that included allExpand
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Has The Time Arrived to Refine The Indications of Immunosuppressive Therapy and Prognosis in IgA Nephropathy?
Immunoglobulin A nephropathy (IgAN) is the most frequent glomerular disease worldwide and a leading cause of end-stage renal disease. Particularly challenging to the clinician is the earlyExpand
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Inherited Risk Factors of Thromboembolic Events in Patients with Primary Nephrotic Syndrome
Background and objectives. Venous thromboembolic events (VTEs) are among the most important complications of nephrotic syndrome (NS). We conducted a study that aimed to determine the prevalence ofExpand
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Familial Mediterranean fever-associated renal amyloidosis: case report and review of the literature.
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease, which is diagnosed especially in Mediterranean patients, but is a rare disorder in our geographical area. Due to itsExpand
Clinical nephrology - miscellaneous
A single-arm pilot study of metformin in patients with autosomal dominant polycystic kidney disease
BackgroundMetformin has shown promising results regarding cystogenesis inhibition in preclinical studies with autosomal dominant polycystic kidney disease (ADPKD) models. We designed a prospective,Expand
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