Received: 2024-02-01
Accepted: 2024-03-05
Published Online: 2024-03-19
Published in Print: 2024-09-25
© 2024 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorial
- Six years of progress – highlights from the IFCC Emerging Technologies Division
- IFCC Papers
- Skin in the game: a review of single-cell and spatial transcriptomics in dermatological research
- Bilirubin measurements in neonates: uniform neonatal treatment can only be achieved by improved standardization
- Validation and verification framework and data integration of biosensors and in vitro diagnostic devices: a position statement of the IFCC Committee on Mobile Health and Bioengineering in Laboratory Medicine (C-MBHLM) and the IFCC Scientific Division
- Linearity assessment: deviation from linearity and residual of linear regression approaches
- HTA model for laboratory medicine technologies: overview of approaches adopted in some international agencies
- Considerations for applying emerging technologies in paediatric laboratory medicine
- A global perspective on the status of clinical metabolomics in laboratory medicine – a survey by the IFCC metabolomics working group
- The LEAP checklist for laboratory evaluation and analytical performance characteristics reporting of clinical measurement procedures
- General Clinical Chemistry and Laboratory Medicine
- Assessing post-analytical phase harmonization in European laboratories: a survey promoted by the EFLM Working Group on Harmonization
- Potential medical impact of unrecognized in vitro hypokalemia due to hemolysis: a case series
- Quantification of circulating alpha-1-antitrypsin polymers associated with different SERPINA1 genotypes
- Targeted ultra performance liquid chromatography tandem mass spectrometry procedures for the diagnosis of inborn errors of metabolism: validation through ERNDIM external quality assessment schemes
- Improving protocols for α-synuclein seed amplification assays: analysis of preanalytical and analytical variables and identification of candidate parameters for seed quantification
- Evaluation of analytical performance of AQUIOS CL flow cytometer and method comparison with bead-based flow cytometry methods
- IgG and kappa free light chain CSF/serum indices: evaluating intrathecal immunoglobulin production in HIV infection in comparison with multiple sclerosis
- Reference Values and Biological Variations
- Reference intervals of circulating secretoneurin concentrations determined in a large cohort of community dwellers: the HUNT study
- Sharing reference intervals and monitoring patients across laboratories – findings from a likely commutable external quality assurance program
- Verification of bile acid determination method and establishing reference intervals for biochemical and haematological parameters in third-trimester pregnant women
- Confounding factors of the expression of mTBI biomarkers, S100B, GFAP and UCH-L1 in an aging population
- Cancer Diagnostics
- Exploring evolutionary trajectories in ovarian cancer patients by longitudinal analysis of ctDNA
- Diabetes
- Evaluation of effects from hemoglobin variants on HbA1c measurements by different methods
- Letters to the Editor
- Are there any reasons to use three levels of quality control materials instead of two and if so, what are the arguments?
- Issues for standardization of neonatal bilirubinemia: a case of delayed phototherapy initiation
- The routine coagulation assays plasma stability – in the wake of the new European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) biological variability database
- Improving HCV diagnosis following a false-negative anti-HCV result
Articles in the same Issue
- Frontmatter
- Editorial
- Six years of progress – highlights from the IFCC Emerging Technologies Division
- IFCC Papers
- Skin in the game: a review of single-cell and spatial transcriptomics in dermatological research
- Bilirubin measurements in neonates: uniform neonatal treatment can only be achieved by improved standardization
- Validation and verification framework and data integration of biosensors and in vitro diagnostic devices: a position statement of the IFCC Committee on Mobile Health and Bioengineering in Laboratory Medicine (C-MBHLM) and the IFCC Scientific Division
- Linearity assessment: deviation from linearity and residual of linear regression approaches
- HTA model for laboratory medicine technologies: overview of approaches adopted in some international agencies
- Considerations for applying emerging technologies in paediatric laboratory medicine
- A global perspective on the status of clinical metabolomics in laboratory medicine – a survey by the IFCC metabolomics working group
- The LEAP checklist for laboratory evaluation and analytical performance characteristics reporting of clinical measurement procedures
- General Clinical Chemistry and Laboratory Medicine
- Assessing post-analytical phase harmonization in European laboratories: a survey promoted by the EFLM Working Group on Harmonization
- Potential medical impact of unrecognized in vitro hypokalemia due to hemolysis: a case series
- Quantification of circulating alpha-1-antitrypsin polymers associated with different SERPINA1 genotypes
- Targeted ultra performance liquid chromatography tandem mass spectrometry procedures for the diagnosis of inborn errors of metabolism: validation through ERNDIM external quality assessment schemes
- Improving protocols for α-synuclein seed amplification assays: analysis of preanalytical and analytical variables and identification of candidate parameters for seed quantification
- Evaluation of analytical performance of AQUIOS CL flow cytometer and method comparison with bead-based flow cytometry methods
- IgG and kappa free light chain CSF/serum indices: evaluating intrathecal immunoglobulin production in HIV infection in comparison with multiple sclerosis
- Reference Values and Biological Variations
- Reference intervals of circulating secretoneurin concentrations determined in a large cohort of community dwellers: the HUNT study
- Sharing reference intervals and monitoring patients across laboratories – findings from a likely commutable external quality assurance program
- Verification of bile acid determination method and establishing reference intervals for biochemical and haematological parameters in third-trimester pregnant women
- Confounding factors of the expression of mTBI biomarkers, S100B, GFAP and UCH-L1 in an aging population
- Cancer Diagnostics
- Exploring evolutionary trajectories in ovarian cancer patients by longitudinal analysis of ctDNA
- Diabetes
- Evaluation of effects from hemoglobin variants on HbA1c measurements by different methods
- Letters to the Editor
- Are there any reasons to use three levels of quality control materials instead of two and if so, what are the arguments?
- Issues for standardization of neonatal bilirubinemia: a case of delayed phototherapy initiation
- The routine coagulation assays plasma stability – in the wake of the new European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) biological variability database
- Improving HCV diagnosis following a false-negative anti-HCV result