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Clinical Biochemistry|May 23, 2013
24 bp duplication of CHIT1 gene and determinants of human chitotriosidase activity among participants of EPISONO, a population-based cross-sectional study, São Paulo, BrazilPriscila Tamanaha, Vânia D'Almeida, Bruno F A Calegare, et al.Clinical Biochemistry|May 29, 2013
Simultaneous determination of phenylalanine and tyrosine in peripheral capillary blood by HPLC with ultraviolet detectionXi-Ming Mo, Ying Li, Ai-Guo Tang, et al.Clinical Biochemistry|May 14, 2013
Development of test strips for rapid buprenorphine detection in vitroSheng-Jin Li, Ding Wang, Jun Zhang, et al.Clinical Biochemistry|June 11, 2013
Comparison between IDMS-traceable Jaffe and enzymatic creatinine assays for estimation of glomerular filtration rate by the CKD-EPI equation in healthy and diabetic subjectsAmanda Veiga Cheuiche, Ariana Aguiar Soares, Eduardo Guimarães Camargo, et al.Clinical Biochemistry|April 30, 2013
The development and characterization of an ELISA specifically detecting the active form of cathepsin KS Sun, M A Karsdal, A C Bay-Jensen, et al.Clinical Biochemistry|September 11, 2014
Red blood cell distribution width and neutrophil/lymphocyte ratio are positively correlated with disease activity in primary Sjögren's syndromeZhi-De Hu, Yi Sun, Jie Guo, et al.Clinical Biochemistry|September 7, 2014
Sensitive detection of trace amounts of KRAS codon 12 mutations by a fast and novel one-step techniqueFeifei Xie, Jie Huang, Shoufang Qu, et al.Clinical Biochemistry|September 8, 2014
Diagnostic performance of cardiac Troponin I for early rule-in and rule-out of acute myocardial infarction: Results of a prospective multicenter trialAlan B Storrow, Robert H Christenson, Richard M Nowak, et al.Clinical Biochemistry|September 26, 2013
Product of serum calcium and phosphorus (Ca × PO4) as predictor of cardiovascular disease risk in predialysis patientsPrashant Regmi, Bimala Malla, Prajwal Gyawali, et al.Clinical Biochemistry|September 25, 2013
Altered red cell and platelet adhesion in hemolytic diseases: Hereditary spherocytosis, paroxysmal nocturnal hemoglobinuria and sickle cell diseaseTatiana M Sakamoto, Andreia A Canalli, Fabiola Traina, et al.Pageof 644