Results 1 to 10 of about 833,453 (214)

The Value of Lactate Dehydrogenase in Predicting Rhabdomyolysis-Induced Acute Renal Failure; a Narrative Review

open access: yesArchives of Academic Emergency Medicine, 2021
Introduction: Determining the diagnostic value of available biomarkers in predicting rhabdomyolysis-induced acute kidney injury (AKI) is a priority. This study aimed to review the current evidence about the value of lactate dehydrogenase (LDH) in this ...
Hazhir Heidari Beigvand   +3 more
doaj   +1 more source

Antibiotic resistance pattern of clinical isolates of ESBL strains and determination of enzymatic relationship with clinical specimen type [PDF]

open access: yesمجله پزشکی دانشگاه علوم پزشکی تبریز, 2020
Background: Differences in clinical isolates may affect the frequency of Extended Spectrum Beta-Lactamase enzymes (ESBLs) in some gram-negative bacteria.
Mahyar Porbaran   +2 more
doaj   +1 more source

Relationship between Paraoxonase-1 and Arylesterase Enzyme Activities and SYNTAX I and II Scores in Patients with ST-Elevation Myocardial Infarction

open access: yesJournal of Tehran University Heart Center, 2019
Background: Although serum paraoxonase-1 (PON-1) and arylesterase (ARE) activities are linked to the presence of stable coronary arterial disease, their correlation with SYNTAX Score I (SS1) and SYNTAX Score II (SS2) has not been known well.
Erdoğan Sökmen   +3 more
doaj   +1 more source

Emerging Approaches for Fluorescence-Based Newborn Screening of Mucopolysaccharidoses

open access: yesDiagnostics, 2020
Interest in newborn screening for mucopolysaccharidoses (MPS) is growing, due in part to ongoing efforts to develop new therapies for these disorders and new screening assays to identify increased risk for the individual MPSs on the basis of deficiency ...
Rajendra Singh   +6 more
doaj   +1 more source

Functional assessment using short tests in a patient with Pompe disease receiving enzyme replacement therapy: case report

open access: yesCase Reports, 2019
Introduction: Pompe disease is characterized by the deficiency of the acid alfa glucosidase enzyme, which leads to a glycogen accumu­lation mainly in cardiac and skeletal muscles.
Thomas Torres-Cuenca   +2 more
doaj   +1 more source

Rapid enzymatic test for phenotypic HIV protease drug resistance [PDF]

open access: yes, 2003
A phenotypic resistance test based on recombinant expression of the active HIV protease in E. coli from patient blood samples was developed. The protease is purified in a rapid onestep procedure as active enzyme and tested for inhibition by five selected
Assfalg-Machleidt, Irmgard   +5 more
core   +1 more source

Clinical and diagnostic significance of activity of enzymes participating in endoergic reactions of patients systemic lupus erythematosus and systemic sclerosis

open access: yesНаучно-практическая ревматология, 2004
Objective. To improve quality of diagnosis of systemic lupus erythematosus (SLE) and systemic sclerosis (SS). Material and methods. 30 pts with SLE and 30 with SS were included.
LA Zborovskaya   +3 more
doaj   +1 more source

Recombinant human G6PD for quality control and quality assurance of novel point-of-care diagnostics for G6PD deficiency. [PDF]

open access: yesPLoS ONE, 2017
BACKGROUND:A large gap for the support of point-of-care testing is the availability of reagents to support quality control (QC) of diagnostic assays along the supply chain from the manufacturer to the end user. While reagents and systems exist to support
Maria Kahn   +13 more
doaj   +1 more source

Epidemiology and the agreement rate of serological tests in human brucellosis in North East of Iran [PDF]

open access: yes, 2015
Background: Brucellosis still remains a major health problem with different symptoms and various diagnostic methods. Diagnostic methods of brucellosis are usually based on detecting specific antibodies in the patient’s serum.
Akhlaghi, M.   +5 more
core   +1 more source

International guidelines for the management and treatment of Morquio A syndrome. [PDF]

open access: yes, 2014
Morquio A syndrome (mucopolysaccharidosis IVA) is a lysosomal storage disorder associated with skeletal and joint abnormalities and significant non-skeletal manifestations including respiratory disease, spinal cord compression, cardiac disease, impaired ...
Berger, Kenneth I   +8 more
core   +2 more sources

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