Is cardiovascular disease in patients with diabetes associated with serum levels of MMP-2, LOX, and the elastin degradation products ELM and ELM-2? [0.03%]
糖尿病患者的心血管疾病与血清基质金属蛋白酶-2、LOX及弹力素降解产物ELM和ELM-2水平有关吗？
Simone Andrea Rørdam Preil,Anne-Sofie Faarvang Thorsen,Anne Lindegaard Christiansen et al.
Simone Andrea Rørdam Preil et al.
Background: Diabetes mellitus type 2 (T2DM) is a significant risk factor for the development of cardiovascular diseases (CVDs). In a previous microarray study of internal mammary arteries from patients with and without T2...
Iron loading in HFE p.C282Y homozygotes found by population screening: relationships to HLA-type and T-lymphocyte subsets [0.03%]
HFE C282Y纯合子铁负荷的研究及其与HLA类型和T淋巴细胞亚型之间的关系
Ketil Thorstensen,Mona A Kvitland,Wenche Ø Irgens et al.
Ketil Thorstensen et al.
Iron loading in p.C282Y homozygous HFE hemochromatosis subjects is highly variable, and it is unclear what factors cause this variability. Finding such factors could aid in predicting which patients are at highest risk and require closest f...
Mortality prediction using serum biomarkers and various clinical risk scales in community-acquired pneumonia [0.03%]
社区获得性肺炎的血清生物标志物及各种临床风险评分的死亡率预测能力研究
Min Woo Kim,Jee Yong Lim,Sang Hoon Oh
Min Woo Kim
We evaluated the predictive value of serum biomarkers and various clinical risk scales for the 28-day mortality of community-acquired pneumonia (CAP). Serum biomarkers including procalcitonin (PCT) and C-reactive protein (CRP) were evaluate...
Paediatric reference values for total homocysteine, tryptophan, tyrosine and phenylalanine in blood spots [0.03%]
血斑中同型半胱氨酸、色氨酸、酪氨酸和苯丙氨酸的儿科参考值
Catharina E Bergwerff,Marjolein Luman,Henk J Blom et al.
Catharina E Bergwerff et al.
Determining blood concentrations of the amino acids homocysteine, tryptophan, tyrosine and phenylalanine in children is of value in the clinical practice. Over the past decades, the use of blood spot samples to examine amino acid concentrat...
K Duus,A H Draborg,E Güven et al.
K Duus et al.
The Farr assay is a radioimmunoassay (RIA) for dsDNA antibodies, based on antibody precipitation using ammonium sulphate and quantification using radio-labelled dsDNA. The RIA-Farr assay offers outstanding clinical specificity and sensitivi...
Biological variation of holotranscobalamin and cobalamin in healthy individuals [0.03%]
健康人血中holotranscobalamin和维生素B12的生物变异性研究
Mette Brokner,Helle Borgstrøm Hager,Morten Lindberg
Mette Brokner
Data on biological variation for cobalamin and holotranscobalamin (holoTC) are limited. The aim of this study was to determine within-subject (CVI) and between-subject (CVG) biological variations for these analytes in a healthy population. ...
Heart-type fatty acid binding protein is a sensitive biomarker for early AMI detection in troponin negative patients: a pilot study [0.03%]
心型脂肪酸结合蛋白是肌钙蛋白阴性患者的急性心肌梗死早期诊断的敏感生物标志物：一项初步研究
Luisa Agnello,Giulia Bivona,Giuseppina Novo et al.
Luisa Agnello et al.
Background: Early detecting AMI in individuals presenting to the ED with chest pain continues to be a challenge. cTn is the gold standard for AMI diagnosis but early presenters (
Comparisons between commercial salivary testosterone enzyme-linked immunosorbent assay kits [0.03%]
商业化唾液睾酮酶联免疫检测试剂盒的比较分析
Christoffer R Andersson,Jonas Bergquist,Elvar Theodorsson et al.
Christoffer R Andersson et al.
Introduction: Measuring testosterone concentrations is of interest both in clinical situations and for research, the latter expanding rapidly during recent years. An increased demand for convenient methods has prompted a ...
HbA1c analysis by capillary electrophoresis - comparison with chromatography and an immunological method [0.03%]
毛细管电泳法分析糖化血红蛋白与色谱法和免疫学方法的比较
Olav Klingenberg,Torill Furuset,Camilla R Hestbråten et al.
Olav Klingenberg et al.
Background: Haemoglobin A1c (HbA1c) has become an even more important analyte for clinical laboratories during recent years with the introduction of its diagnostic use for diabetes mellitus. Several different analytical p...
Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluation [0.03%]
希腊半乳糖血症患者GALT基因突变分析及临床评估
Kleopatra H Schulpis,Georgia Thodi,Konstantinos Iakovou et al.
Kleopatra H Schulpis et al.
Classical galactosaemia is an inborn error of metabolism due to the deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT). The aim of the study was to identify the underlying mutations in Greek patients with GALT deficie...