Search Results - "Kukuy, Olga"
-
1
Diagnostic Challenges and Solutions in Systemic Amyloidosis
Published in International journal of molecular sciences (28-02-2023)“…Amyloidosis refers to a clinically heterogeneous group of disorders characterized by the extracellular deposition of amyloid proteins in various tissues of the…”
Get full text
Journal Article -
2
Amyloid storm: acute kidney injury and massive proteinuria, rapidly progressing to end-stage kidney disease in AA amyloidosis of familial Mediterranean fever
Published in Rheumatology (Oxford, England) (01-07-2021)“…Abstract Objective Amyloid A nephropathy of FMF usually progresses over many years to end-stage renal disease (ESRD). We aim to describe an acute condition,…”
Get full text
Journal Article -
3
Anakinra for Colchicine‐Resistant Familial Mediterranean Fever: A Randomized, Double‐Blind, Placebo‐Controlled Trial
Published in Arthritis & rheumatology (Hoboken, N.J.) (01-04-2017)“…Objective Familial Mediterranean fever (FMF) is refractory to colchicine prophylaxis in 10–20% of patients. In a number of patient series, treatment with…”
Get full text
Journal Article -
4
Treatment of Severe Renal Artery Stenosis with Acute Kidney Injury Requiring Hemodialysis by Percutaneous Transluminal Renal Angioplasty and Stent Implantation
Published in Journal of vascular and interventional radiology (01-06-2022)“…To evaluate the outcomes of percutaneous transluminal renal angioplasty with stent implantation (PTRAS) among patients with renal artery stenosis (RAS) who…”
Get full text
Journal Article -
5
Familial Mediterranean fever without MEFV mutations: a case-control study
Published in Orphanet journal of rare diseases (25-03-2015)“…Although familial Mediterranean fever (FMF) was originally defined as an autosomal recessive disorder, approximately 10-20% of FMF patients do not carry any…”
Get full text
Journal Article -
6
Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot study
Published in Clinical chemistry and laboratory medicine (26-02-2024)“…Diagnosis of light chain amyloidosis (AL) requires demonstration of amyloid deposits in a tissue biopsy followed by appropriate typing. Previous studies…”
Get more information
Journal Article -
7
Patients with CKD Secondary to Glomerular Disorders have Lower Arterial Stiffness, as Compared to Hypertensive and Diabetic CKD
Published in Artery research (01-09-2023)“…Background Chronic kidney disease (CKD) manifested as reduced GFR and/or albuminuria, has been known to accelerate arterial stiffness and early vascular aging…”
Get full text
Journal Article -
8
Kidney disease and plasma cell dyscrasias: ambiguous cases solved by serum free light chain dimerization analysis
Published in Clinical and experimental nephrology (01-06-2019)“…Background Plasma cell dyscrasias (PCD) comprise a wide spectrum of disorders, which may adversely affect the kidney. However, in some PCD cases associated…”
Get full text
Journal Article -
9
The Prognostic Value of Anti-PLA2R Antibodies Levels in Primary Membranous Nephropathy
Published in International journal of molecular sciences (21-05-2023)“…Anti-PLA2R antibodies (Ab) are a diagnostic and prognostic biomarker in primary membranous nephropathy (PMN). We assessed the relationship between the levels…”
Get full text
Journal Article -
10
Serum amyloid A levels in kidney-transplanted patients with familial Mediterranean fever-amyloidosis
Published in The Israel Medical Association journal (01-04-2011)“…Amyloidosis of familial Mediterranean fever (FMF) may lead to end-stage renal failure, culminating in kidney transplantation. Since amyloidosis is prompted by…”
Get full text
Journal Article -
11
PS-P15-3: PATIENTS WITH GLOMERULONEPHRITIS IN REMISSION HAVE DECREASED ARTERIAL STIFFNESS COMPARED TO CKD PATIENTS
Published in Journal of hypertension (01-01-2023)“…Background: Arterial stiffness is the hallmark of the vascular aging process, in which a disruption in collagen to elastin balance in the large arteries with…”
Get full text
Journal Article -
12
The use of serum free light chain dimerization patterns assist in the diagnosis of AL amyloidosis
Published in British journal of haematology (01-07-2018)“…Summary The discrimination between benign and malignant forms of plasma cell dyscrasia (PCD) is often difficult. Free light chain monomer‐dimer pattern…”
Get full text
Journal Article -
13
Familial Mediterranean Fever (FMF) with Proteinuria: Clinical Features, Histology, Predictors, and Prognosis in a Cohort of 25 Patients
Published in Journal of rheumatology (01-12-2013)“…Reactive (AA) amyloidosis may complicate familial Mediterranean fever (FMF), the prototype of autoinflammatory diseases. Thus, proteinuria in FMF is commonly…”
Get full text
Journal Article -
14
Listeria Peritonitis in a Patient Treated with Peritoneal Dialysis
Published in The Israel Medical Association journal (01-02-2016)Get full text
Journal Article -
15
Immunoglobulin‐free light chain monomer‐dimer patterns help to distinguish malignant from premalignant monoclonal gammopathies: A pilot study
Published in American journal of hematology (01-09-2014)“…Multiple myeloma (MM) and AL amyloidosis (AL) are two malignant forms of monoclonal gammopathies. For the purposes of prognosis and treatment, it is important…”
Get full text
Journal Article -
16
Prevalence of severe mitral regurgitation eligible for edge-to-edge mitral valve repair (MitraClip)
Published in Clinical research in cardiology (01-08-2016)“…Objectives We assessed the prevalence of moderately severe or severe mitral regurgitation (MR) justifying edge-to-edge mitral valve (MV) repair (MitraClip ® )…”
Get full text
Journal Article -
17
Normal arterial stiffness in familial Mediterranean fever. Evidence for a possible cardiovascular protective role of colchicine
Published in Clinical and experimental rheumatology (01-11-2017)“…Familial Mediterranean fever (FMF) is an autoinflammatory disorder with episodic and persistent inflammation, which is only partially suppressed by continuous…”
Get full text
Journal Article -
18
Acquired familial Mediterranean fever associated with a somatic MEFV mutation in a patient with JAK2 associated post-polycythemia myelofibrosis
Published in Orphanet journal of rare diseases (30-06-2015)“…A study was designed to identify the source of fever in a patient with post-polycythemia myelofibrosis, associated with clonal Janus Kinase 2 (JAK2) mutation…”
Get full text
Journal Article