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Autoantibodies are not associated with familial mediterranean fever
(MEDFARMA-EDICOES MEDICAS, LDA, 2012)
Objective: It has been suggested that Mediterranean fever (MEFV) gene mutations are also seen in certain autoimmune diseases and are related to severity of the disease activity. As most of the clinical symptoms of these ...
Mesangioproliferative Glomerulonephritis Due to Hepatic Hydatid Disease: A Case Report and Literature Review
(TURK NEFROLOJI DIYALIZ TRANSPLANTASYON DERGISI, 2015)
Hydatid cyst (CH), which is quite common in the world, mostly transmitted by dog faeces, is a parasitic disease caused by Echinococcus granulosus. CH often infects the liver and lungs. During the clinical course, renal ...
Glutathione-S-Transferase Variants are not Associated With Increased Carotid Intima-Media Thickness in Turkish Familial Mediterranean Fever Patients
(TURKISH LEAGUE AGAINST RHEUMATISM, 2016)
Objectives: This study aims to evaluate the carotid intima-media thickness (CIMT) in patients diagnosed with familial Mediterranean fever (FMF) and investigate whether there is a relationship between glutathione-S-transferase ...
Coexistence of Systemic Lupus Erythematosus and Familial Mediterranean Fever
(JAPAN SOC INTERNAL MEDICINE, 2010)
Clinical symptoms and findings of familial Mediterranean fever (FMF), occur as a result of autoimmune inflammation of the serous membrane which is also seen in systemic lupus erythematosus (SLE). Difficulties are sometimes ...
Factors Related to Microalbuminuria in Patients with Chronic Obstructive Pulmonary Disease
(WROCLAW MEDICAL UNIV, 2014)
Background. Chronic obstructive pulmonary disease (COPD) is characterized by inhaled particles and gases inducing chronic inflammation of the airways accompanied by a not fully reversible airflow limitation. Systemic ...
Gitelman's syndrome associated with chondrocalcinosis: a case report
(INFORMA HEALTHCARE, 2013)
Gitelman's syndrome (GS) is a rare disease with autosomal recessive trait, characterized by hypokalemia, hypomagnesemia, metabolic alkalosis, hypocalciuria and hyperkinemic hyperaldosteronism. While muscle weakness, tetany, ...
Catheter-Related Bacteremia due to Enterobacter ludwigii in a Hemodialysis Patient: First Report in the Literature
(TURK NEFROLOJI DIYALIZ TRANSPLANTASYON DERGISI, 2018)
The Enterobacter cloacae complex, a member of the genus Enterobacter, consists of a group of bacteria that are responsible for serious infections in human beings. A recently identified member of the group, Enterobacter ...
Role of the VEGF 936 gene polymorphism and VEGF-A levels in the late-term arteriovenous fistula thrombosis in patients undergoing hemodialysis
(SPRINGER, 2014)
Vascular access is vital for hemodialysis patients. A major factor that facilitates arteriovenous (AV) fistula failure is stenosis and thrombosis due to intimal hyperplasia developing in the venous segment of AV fistula. ...
What Is the Meaning of Increased Myocardial Injury Enzymes during Hemodialysis? A Tissue Doppler Imaging Study
(KARGER, 2013)
Background: Cardiovascular death is decreasing in the general population; however, it appears in still higher rates and even increases gradually in hemodialysis (HD) patients. This situation has led to a debate about ...
Association between ABCB1 (MDR1) Gene 3435 C > T Polymorphism and Colchicine Unresponsiveness of FMF Patients
(TAYLOR & FRANCIS LTD, 2011)
The multidrug resistance gene-1 (MDR1, adenosine triphosphate-binding cassette transporter: ABCB1, P-glycoprotein) encodes membrane proteins that play a crucial role in protecting cells from xenobiotics, chemicals, and ...