Претраживање
Приказ резултата 1-4 од 4
Isoelectrofocusing and PCR Amplification-Reverse Hybridization Assay in Evaluation of Alpha-1-Antitrypsin Deficiency
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
Alpha-1-antitrypsin deficiency is a potentially lethal genetic disorder, which has pulmonary and liver manifestations. The standardized biochemical and molecular diagnostic protocol for detection of clinically relevant ...
Incidence of hyperhomocysteinemia and Mthfr C677T polymorphism among young patients with acute myocardial infarction
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
Hyperhomocysteinemia is considered an independent risk factor for premature cardiovascular disease. Mutation MTHFR C677T reduces the activity of methylenetetra-hydrofolatereductase and may cause hyperhomocysteinemia. ...
Methotrexate-associated biochemical alterations in a patient with chronic neurotoxicity
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
Intrathecal and/or high-dose intravenous administration of methotrexate (MTX) in the treatment of malignancies such as acute lymphoblastic leukaemia (ALL) has been associated with cases of mild to severe neurotoxicity. The ...
Hyperhomocysteinemia and smoking in primary antiphospholipid syndrome
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
The thrombotic tendency in anti phospholipid syndrome (APS) shares several pathways with atherosclerosis. Atherothrombosis (atherosclerosis superimposed with thromboses) is influenced by nonmodifiable and some modifiable ...