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The role of liquid chromatography–tandem mass spectrometry in the clinical laboratory

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2012-02, Vol.883-884, p.18-32

2012

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Multicenter comparison study of current methods to measure 25-hydroxyvitamin D in serum

Steroids, 2012-11, Vol.77 (13), p.1366-1372

2012

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Evaluation of 3-epi-25-hydroxyvitamin D3 cross-reactivity in the Roche Elecsys Vitamin D Total protein binding assay

Clinical chemistry and laboratory medicine, 2014-03, Vol.52 (3), p.373

2014

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Analysis of vitamin D metabolites by liquid chromatography-tandem mass spectrometry

TrAC, Trends in analytical chemistry (Regular ed.), 2016-11, Vol.84, p.117-130

van den Ouweland, Johannes M.W.

2016

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Overestimation of 25-hydroxyvitamin D3 by increased ionisation efficiency of 3-epi-25-hydroxyvitamin D3 in LC–MS/MS methods not separating both metabolites as determined by an LC–MS/MS method for separate quantification of 25-hydroxyvitamin D3, 3-epi-25-hydroxyvitamin D3 and 25-hydroxyvitamin D2 in human serum

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2014-09, Vol.967, p.195-202

2014

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Thyroglobulin (Tg) Recovery Testing with Quantitative Tg Antibody Measurement for Determining Interference in Serum Tg Assays in Differentiated Thyroid Carcinoma

Clinical chemistry (Baltimore, Md.), 2006-06, Vol.52 (6), p.1196-1199

2006

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Measurement of 25-OH-vitamin D in human serum using liquid chromatography tandem-mass spectrometry with comparison to radioimmunoassay and automated immunoassay

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2010-05, Vol.878 (15), p.1163-1168

2010

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Vitamin D and metabolites measurement by tandem mass spectrometry

Reviews in endocrine & metabolic disorders, 2013-06, Vol.14 (2), p.159-184

2013

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Clinical Utility of an Automated Immunochemiluminometric Thyroglobulin Assay in Differentiated Thyroid Carcinoma

Clinical chemistry (Baltimore, Md.), 2006-04, Vol.52 (4), p.686-691

2006

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Detection of Mitochondrial DNA Deletions in Human Skin Fibroblasts of Patients with Pearson's Syndrome by Two-color Fluorescence In Situ Hybridization

The journal of histochemistry and cytochemistry, 1997-01, Vol.45 (1), p.55-61

1997

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Time-course analysis of 3-epi-25-hydroxyvitamin D3 shows markedly elevated levels in early life, particularly from vitamin D supplementation in preterm infants

Pediatric research, 2016-04, Vol.79 (4), p.647-653

2016

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Plasma citrulline measurement using UPLC tandem mass-spectrometry to determine small intestinal enterocyte pathology

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2009-02, Vol.877 (4), p.387-392

2009

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The new Roche Vitamin D Total assay: fit for its purpose?

Clinical chemistry and laboratory medicine, 2012-11, Vol.50 (11), p.1969-1972

2012

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Evaluation of 3-epi-25-hydroxyvitamin D 3 cross-reactivity in the Roche Elecsys Vitamin D Total protein binding assay

Clinical chemistry and laboratory medicine, 2014-03, Vol.52 (3), p.373-380

2014

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High total protein impairs appropriate gel barrier formation in BD Vacutainer blood collection tubes

Clinical chemistry (Baltimore, Md.), 2007-02, Vol.53 (2), p.364-365

2007

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Unanticipated error in HbA1c measurement on the HLC-723 G7 analyzer

Clinical biochemistry, 2010-04, Vol.43 (6), p.623-625

2010

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Unanticipated error in HbA 1c measurement on the HLC-723 G7 analyzer

Clinical biochemistry, 2010, Vol.43 (6), p.623-625

2010

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The silent hemoglobin α chain variant Hb Riccarton [α51(CE9)Gly→Ser] may affect HbA1c determination on the HLC-723 G7 analyzer

Clinical chemistry and laboratory medicine, 2008-01, Vol.46 (6), p.827-830

2008

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The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate

The Journal of biological chemistry, 1999-10, Vol.274 (42), p.29744-29748

1999

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Molecular Characterization of WFS1 in Patients with Wolfram Syndrome

The Journal of molecular diagnostics : JMD, 2003-05, Vol.5 (2), p.88-95

2003

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Mitochondrial diabetes mellitus: a review

Biochimica et biophysica acta, 1995-05, Vol.1271 (1), p.253-260

1995

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Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene

Diabetes (New York, N.Y.), 1994-06, Vol.43 (6), p.746-751

1994

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Validation study of Axis-Shield carbohydrate-deficient transferrin (CDT) on ARCHITECT® chemistry analyzer

Clinical chemistry and laboratory medicine, 2007-01, Vol.45 (11), p.1555-1558

2007

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The Diabetes-associated 3243 Mutation in the Mitochondrial tRNALeu(UUR) Gene Causes Severe Mitochondrial Dysfunction without a Strong Decrease in Protein Synthesis Rate

The Journal of biological chemistry, 1999-10, Vol.274 (42), p.29744-29748

1999

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Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene

Diabetes (New York, N.Y.), 1994-06, Vol.43 (6), p.746-751

1994

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The role of liquid chromatography–tandem mass spectrometry in the clinical laboratory

Multicenter comparison study of current methods to measure 25-hydroxyvitamin D in serum

Evaluation of 3-epi-25-hydroxyvitamin D3 cross-reactivity in the Roche Elecsys Vitamin D Total protein binding assay

Analysis of vitamin D metabolites by liquid chromatography-tandem mass spectrometry

Thyroglobulin (Tg) Recovery Testing with Quantitative Tg Antibody Measurement for Determining Interference in Serum Tg Assays in Differentiated Thyroid Carcinoma

Measurement of 25-OH-vitamin D in human serum using liquid chromatography tandem-mass spectrometry with comparison to radioimmunoassay and automated immunoassay

Vitamin D and metabolites measurement by tandem mass spectrometry

Clinical Utility of an Automated Immunochemiluminometric Thyroglobulin Assay in Differentiated Thyroid Carcinoma

Detection of Mitochondrial DNA Deletions in Human Skin Fibroblasts of Patients with Pearson's Syndrome by Two-color Fluorescence In Situ Hybridization

Time-course analysis of 3-epi-25-hydroxyvitamin D3 shows markedly elevated levels in early life, particularly from vitamin D supplementation in preterm infants

Plasma citrulline measurement using UPLC tandem mass-spectrometry to determine small intestinal enterocyte pathology

The new Roche Vitamin D Total assay: fit for its purpose?

Evaluation of 3-epi-25-hydroxyvitamin D 3 cross-reactivity in the Roche Elecsys Vitamin D Total protein binding assay

High total protein impairs appropriate gel barrier formation in BD Vacutainer blood collection tubes

Unanticipated error in HbA1c measurement on the HLC-723 G7 analyzer

Unanticipated error in HbA 1c measurement on the HLC-723 G7 analyzer

The silent hemoglobin α chain variant Hb Riccarton [α51(CE9)Gly→Ser] may affect HbA1c determination on the HLC-723 G7 analyzer

The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate

Molecular Characterization of WFS1 in Patients with Wolfram Syndrome

Mitochondrial diabetes mellitus: a review

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene

Validation study of Axis-Shield carbohydrate-deficient transferrin (CDT) on ARCHITECT® chemistry analyzer

The Diabetes-associated 3243 Mutation in the Mitochondrial tRNALeu(UUR) Gene Causes Severe Mitochondrial Dysfunction without a Strong Decrease in Protein Synthesis Rate

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene

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