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Endocrinology Unit 2, University of Pisa, Pisa, Italy
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Laboratory of Clinical Pathology, University Hospital of Pisa, Pisa, Italy
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and the majority of routine analyses are performed all over the world by immunoassay techniques, which allow non-chromatographic quantification of total 25 Hydroxyvitamin D (25OHD). In recent years, liquid chromatography-tandem mass spectrometry (LC
Department of Clinical Science, Department of Medicine, University of Bergen, N-5021 Bergen, Norway
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Department of Clinical Science, Department of Medicine, University of Bergen, N-5021 Bergen, Norway
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Department of Clinical Science, Department of Medicine, University of Bergen, N-5021 Bergen, Norway
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factors likely to slow its adoption. The development of simple, reliable, and cost- and labour-efficient methods is, therefore, important. Liquid chromatography coupled to tandem mass spectrometry (LC–MS/MS) is a highly selective mode of detection. It
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, interquartile range; LC-MS/MS, liquid chromatography with tandem mass spectrometry. Considering the CLIA method, patients with TP had statistically higher concentrations of 25(OH)D than patients with SP. However, regarding the results of LC
Department of Laboratory Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands
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chromatography tandem mass spectrometry (ED-LC-MS/MS). LC-MS/MS enables the accurate, specific and matrix-independent measurement of testosterone with direct calibration. Equilibrium dialysis enables to separate the free- from protein-bound testosterone with
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-segment changes in some leads, T-wave changes in some leads, and low voltage in the left chest lead. The purpose of this study was to examine the distinct metabolite profiles of plasma among these groups using liquid chromatography–mass spectrometry (LC-MS) to
Inserm U1016-CNRS UMR8104, Paris, France
Hormonology Department, Cochin Hospital, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Radiology Department, Cochin Hospital, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Reference Center for Rare Adrenal Diseases, Endocrinology Department, Cochin Hospital, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Reference Center for Rare Adrenal Diseases, Endocrinology Department, Cochin Hospital, Paris, France
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Hormonology Department, Cochin Hospital, Paris, France
INSERM, Physiopathologie et Pharmacotoxicologie Placentaire Humaine : Microbiote Pré & Post natal, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Diabetology Department, Cochin Hospital, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Reference Center for Rare Adrenal Diseases, Endocrinology Department, Cochin Hospital, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Reference Center for Rare Adrenal Diseases, Endocrinology Department, Cochin Hospital, Paris, France
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Hormonology Department, Cochin Hospital, Paris, France
INSERM, Physiopathologie et Pharmacotoxicologie Placentaire Humaine : Microbiote Pré & Post natal, Paris, France
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UR 7537 BioSTM, Paris, France
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Inserm U1016-CNRS UMR8104, Paris, France
Reference Center for Rare Adrenal Diseases, Endocrinology Department, Cochin Hospital, Paris, France
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nitrogen. Dried extracts were further reconstituted in 100 µL of MeOH/water (50/50). Conditions and instrumentation for ultra-high-performance liquid chromatography-mass spectrometry Steroid profiles were characterized using LC-MS/MS. Ten
Birmingham Women’s Foundation Hospital, Edgbaston, Birmingham, UK
Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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Birmingham Women’s Foundation Hospital, Edgbaston, Birmingham, UK
Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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stored at −80°C until use. Quantitative analysis of urinary de-conjugated vitamin D metabolites in spot urine samples was performed using a novel liquid chromatography tandem-mass spectrometry (LC–MS/MS) methodology. This was optimised from a method
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specificity ( 4 , 5 , 6 ). Cortisol analyses using liquid chromatography tandem mass spectrometry (LC-MS/MS) have eliminated the problems of cross-reactivity with exogenous steroids and cortisol metabolites often found with immunoassays ( 7 , 8 , 9 , 10
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-of-the-art liquid chromatography–tandem mass spectrometry (LC–MS/MS) ( 20 ). This method can quantify 11 sulfated steroids simultaneously, providing a powerful tool to understand the sulfated steroidome in human blood ( 21 ). We hypothesized that sulfated steroids
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involved in the tryptophan metabolism by liquid chromatography−mass spectrometry (LC-MS). Methods Sample selection Patients were included from the Erasmus Medical Center NET database. The study was performed retrospectively, and, according to