Works by Byeon, Seul
Results: 10
An exploratory study of plasma ceramides in comorbidities in Down syndrome.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 9, p. 2300, doi. 10.1002/ajmg.a.63325
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- Article
Computational approach to structural identification of phospholipids using raw mass spectra from nanoflow liquid chromatography-electrospray ionization-tandem mass spectrometry.
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- Journal of Mass Spectrometry, 2012, v. 47, n. 8, p. 1004, doi. 10.1002/jms.3033
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- Article
A multiplexed targeted method for profiling of serum gangliosides and glycosphingolipids: application to GM2-gangliosidosis.
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- Analytical & Bioanalytical Chemistry, 2024, v. 416, n. 26, p. 5689, doi. 10.1007/s00216-024-05487-3
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- Article
Lipidomic differentiation of Graves’ ophthalmopathy in plasma and urine from Graves’ disease patients.
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- Analytical & Bioanalytical Chemistry, 2018, v. 410, n. 27, p. 7121, doi. 10.1007/s00216-018-1313-2
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- Article
Exploring therapeutic strategies for infantile neuronal axonal dystrophy (INAD/PARK14).
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.82555
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- Article
Development of a Multiplexed Sphingolipids Method for Diagnosis of Inborn Errors of Ceramide Metabolism.
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- Clinical Chemistry, 2024, v. 70, n. 11, p. 1366, doi. 10.1093/clinchem/hvae115
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- Article
Evaluation of treadmill exercise effect on muscular lipid profiles of diabetic fatty rats by nanoflow liquid chromatography-tandem mass spectrometry.
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- Scientific Reports, 2016, p. 29617, doi. 10.1038/srep29617
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- Article
High-throughput and rapid quantification of lipids by nanoflow UPLC-ESI-MS/MS: application to the hepatic lipids of rabbits with nonalcoholic fatty liver disease.
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- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 18, p. 4975, doi. 10.1007/s00216-016-9592-y
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- Article
Variations in plasma and urinary lipids in response to enzyme replacement therapy for Fabry disease patients by nanoflow UPLC-ESI-MS/MS.
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- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 9, p. 2265, doi. 10.1007/s00216-016-9318-1
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- Article
TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels.
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- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 6, p. 1039, doi. 10.1002/jimd.12550
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- Article