Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Dietmar Stöckl"'
Autor:
Hedwig C M, Stepman, Ulla, Tiikkainen, Dietmar, Stöckl, Hubert W, Vesper, Selvin H, Edwards, Harri, Laitinen, Jonna, Pelanti, Linda M, Thienpont, Marzena, Modzelewska
Publikováno v:
Clinical Chemistry. 60:855-863
BACKGROUNDExternal quality assessment (EQA) with commutable samples is essential for assessing the quality of assays performed by laboratories, particularly when the emphasis is on their standardization status and interchangeability of results.METHOD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995687e4048ca72dcf00d822c0077d2d
https://doi.org/10.1373/clinchem.2013.220376
https://doi.org/10.1373/clinchem.2013.220376
Publikováno v:
cclm. 49:253-256
Background: Since the introduction of liquid chromatography-mass spectrometry (LC/MS) for assessing vitamin D status, it has been shown that the C-3 epimer can account for a significant proportion of circulating 25-hydroxyvitamin D3 (25OHD3) concentr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cd38ac402e3e22932100a4a68b81356
https://doi.org/10.1515/cclm.2011.050
https://doi.org/10.1515/cclm.2011.050
Publikováno v:
Clinica Chimica Acta. 408:8-13
Background The divergence in analytical quality of serum/plasma 25-hydroxy-vitamin D analysis calls for defining specifications for a reference measurement system. Methods Fundamentally, in a reference measurement system, there should be a relationsh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35d827e543eb4a69c5f9027ddd3f421e
https://doi.org/10.1016/j.cca.2009.06.027
https://doi.org/10.1016/j.cca.2009.06.027
Publikováno v:
Journal of Chromatography B. 877:2180-2190
Analytical method development should aim at delivering reliable measurements within a given application. This implies that method validation is integrated in the development process, because it enables to establish a method's performance capabilities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aef745dfdeee484f71245c35a0f127c
https://doi.org/10.1016/j.jchromb.2008.12.056
https://doi.org/10.1016/j.jchromb.2008.12.056
Autor:
Katleen Van Uytfanghe, Dietmar Stöckl, Linde A.C. De Grande, Kenneth Goossens, Linda M. Thienpont
Publikováno v:
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Manufacturers and laboratories might benefit from using a modern integrated tool for quality management/assurance. The tool should not be confounded by commutability issues and focus on the intrinsic analytical quality and comparability of assays as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ece386c16d9598e2b551d8caafc24d2
https://doi.org/10.1515/cclm-2014-0959
https://doi.org/10.1515/cclm-2014-0959
Publikováno v:
Clinical Chemistry. 52:1193-1196
Background: Serum C-peptide concentrations reflect pancreatic function in different clinical and diagnostic settings; however, the utility of C-peptide testing is limited by the lack of standardized commercial immunoassays. Standardization can best b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75a270225f298429e310b8ad3cae453
https://doi.org/10.1373/clinchem.2005.062505
https://doi.org/10.1373/clinchem.2005.062505
Autor:
Tom Fiers, Jean-Marc Kaufman, A.P. De Leenheer, K. Van Uytfanghe, Linda M. Thienpont, Dietmar Stöckl
Publikováno v:
Clinical Biochemistry. 38:253-261
Background/Method: The analytical validity of free testosterone (FTe) analog immunoassays is subject to much controversy. We revisited the validation of 4 analog assays and 1 FTe calculation procedure with a metrologically traceable reference measure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31727a492e15a127dc0e86ba2631690d
https://doi.org/10.1016/j.clinbiochem.2004.12.001
https://doi.org/10.1016/j.clinbiochem.2004.12.001
Autor:
Linda M. Thienpont, Pål Rustad, Dietmar Stöckl, Thomas Røraas, Gunn B.B. Kristensen, Sverre Sandberg, Sofie K. Van Houcke, Hedwig Stepman
Publikováno v:
Clinical Chemistry. 58:1597-1599
To the Editor: The scope of external quality assessment (EQA)1 in laboratory medicine has evolved considerably (1). With the increasing worldwide interest in the use of common reference intervals and/or medical-decision limits, modern EQA schemes nee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64466f635d805520c7808c20b434f55d
https://doi.org/10.1373/clinchem.2012.189670
https://doi.org/10.1373/clinchem.2012.189670
Publikováno v:
Clinical Nephrology. 58:205-210
Aim of the study: Based on data in the literature, it remains unclear whether the ionized fraction of serum total magnesium (Mg) is lower in chronic hemodialysis (HD) patients compared to healthy subjects. Patients and methods: The ionized fraction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8930da2c30078b331505918744a1d75
https://doi.org/10.5414/cnp58205
https://doi.org/10.5414/cnp58205
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 52
Background: Between-method equivalence ideally is achieved by calibration against an SI-traceable reference measurement procedure. For measurement of thyroid stimulating hormone (TSH), it is unlikely to accomplish this goal in mid-term. Therefore, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ed5911a96d55be920d4349693c0a3d
https://doi.org/10.1515/cclm-2013-1038
https://doi.org/10.1515/cclm-2013-1038