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An improved high-throughput liquid chromatographic/tandem mass spectrometric method for terbinafine quantification in human plasma, using automated liquid-liquid extraction based on 96-well format plates.
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- Biomedical Chromatography, 2007, v. 21, n. 2, p. 201, doi. 10.1002/bmc.738
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- Article
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screening.
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- Journal of Human Genetics, 2011, v. 56, n. 12, p. 861, doi. 10.1038/jhg.2011.119
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- Article
Quantitation and evaluation of perinatal medium-chain and long-chain acylcarnitine blood concentrations in 12,000 full-term breastfed newborns.
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- Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 8, p. 1023, doi. 10.1515/jpem-2020-0741
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- Article
Birth weight related blood concentrations of the neurotransmission amino acids glutamine plus glutamate, phenylalanine and tyrosine in full-term breastfed infants perinatally.
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- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 3, p. 367, doi. 10.1515/jpem-2019-0522
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- Article
Nutrition and medical support during pregnancy and lactation in women with inborn errors of intermediary metabolism disorders (IEMDs).
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- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 1, p. 5, doi. 10.1515/jpem-2019-0048
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- Article
Quantitation of the arginine family amino acids in the blood of full-term infants perinatally in relation to their birth weight.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 8, p. 803, doi. 10.1515/jpem-2019-0146
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- Article
Classical galactosemia patients can achieve high IQ scores.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 4, p. 399, doi. 10.1515/jpem-2018-0515
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- Article
Identification of five mutations in a patient with galactose metabolic disorders.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 221, doi. 10.1515/jpem-2017-0438
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- Article
Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
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- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 10, p. 1119, doi. 10.1515/jpem-2017-0263
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- Article
Clinical evaluation and mutational analysis of GALK and GALE genes in patients with galactosemia in Greece: one novel mutation and two rare cases.
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- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 7, p. 775, doi. 10.1515/jpem-2017-0065
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- Article
Partial biotinidase deficiency: identification of a single novel mutation (p.H314R) in a Greek newborn.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 3, p. 389, doi. 10.1515/jpem-2015-0387
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- Article
Hawkinsinuria in two unrelated Greek newborns: identification of a novel variant, biochemical findings and treatment.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 1, p. 15, doi. 10.1515/jpem-2015-0132
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- Article
Early screening of FTO and MC4R variants in newborns of Greek origin.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 5/6, p. 619, doi. 10.1515/jpem-2014-0320
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- Article
Homologous Recombination Deficiency Score Determined by Genomic Instability in a Romanian Cohort.
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- Diagnostics (2075-4418), 2023, v. 13, n. 11, p. 1896, doi. 10.3390/diagnostics13111896
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- Article
Dried plasma spots as an alternative sample collection technique for the quantitative LC-MS/MS determination of gabapentin.
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- Analytical & Bioanalytical Chemistry, 2010, v. 398, n. 3, p. 1339, doi. 10.1007/s00216-010-4048-2
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- Article
Simultaneous determination of losartan, EXP-3174 and hydrochlorothiazide in plasma via fully automated 96-well-format-based solid-phase extraction and liquid chromatography–negative electrospray tandem mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2007, v. 387, n. 2, p. 593, doi. 10.1007/s00216-006-0990-4
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- Article
Development of a high-throughput method for the determination of itraconazole and its hydroxy metabolite in human plasma, employing automated liquid–liquid extraction based on 96-well format plates and LC/MS/MS.
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- Analytical & Bioanalytical Chemistry, 2005, v. 384, n. 1, p. 199, doi. 10.1007/s00216-005-0159-6
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- Article
Comparison of hydrophilic interaction and reversed-phase liquid chromatography coupled with tandem mass spectrometric detection for the determination of three pharmaceuticals in human plasma.
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- Biomedical Chromatography, 2008, v. 22, n. 12, p. 1393, doi. 10.1002/bmc.1071
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- Article
Validation of a fully automated high throughput liquid chromatographic/tandem mass spectrometric method for roxithromycin quantification in human plasma. Application to a bioequivalence study.
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- Biomedical Chromatography, 2008, v. 22, n. 5, p. 494, doi. 10.1002/bmc.958
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- Article
Increased blood concentrations of neurotransmission amino acids and modulation of specific enzyme activities after resistance and endurance exercise.
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- Sport Sciences for Health, 2020, v. 16, n. 2, p. 217, doi. 10.1007/s11332-020-00648-0
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- Article
Expanded newborn screening in Greece: 30 months of experience.
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- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 341, doi. 10.1007/s10545-010-9181-8
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- Article
Validation of a novel LC-MS/MS method for the quantitation of colistin A and B in human plasma.
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- Journal of Separation Science, 2011, v. 34, n. 1, p. 37, doi. 10.1002/jssc.201000680
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- Article
Dried Blood Spots in Neonatal Studies: A Computational Analysis for the Role of the Hematocrit Effect.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 8, p. 1126, doi. 10.3390/ph16081126
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- Article
Development of a rapid method for the determination of glimepiride in human plasma using liquid-liquid extraction based on 96-well format micro-tubes and liquid chromatography/tandem mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 2005, v. 19, n. 14, p. 2055, doi. 10.1002/rcm.2028
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- Article