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Pediatrics|May 1, 1993
Clinical and biochemical phenotype in 11 patients with mevalonic aciduriaG F Hoffmann, C Charpentier, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Journal of Inherited Metabolic Disease|August 18, 2009
Mental retardation and inborn errors of metabolismA García-Cazorla, N I Wolf, M Serrano, et al.
Free Radical Biology & Medicine|December 4, 2003
Beta-carotene cleavage products after oxidation mediated by hypochlorous acid--a model for neutrophil-derived degradationOlaf Sommerburg, Claus-Dieter Langhans, Jürgen Arnhold, et al.
International Journal of Molecular Sciences|September 28, 2021
A Novel UPLC-MS/MS Method Identifies Organ-Specific Dipeptide ProfilesElena Heidenreich, Tilman Pfeffer, Tamara Kracke, et al.
Plos Pathogens|February 3, 2025
Quinoxaline-based anti-schistosomal compounds have potent anti-plasmodial activityMukul Rawat, Gilda Padalino, Edem Adika, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 16, 2018
Quantification of methylcitrate in dried urine spots by liquid chromatography tandem mass spectrometry for the diagnosis of propionic and methylmalonic acidemiasNahid Al Dhahouri, Claus-Dieter Langhans, Zalikha Al Hammadi, et al.
International Journal of Neonatal Screening|December 27, 2024
Digital-Tier Strategy Improves Newborn Screening for Glutaric Aciduria Type 1Elaine Zaunseder, Julian Teinert, Nikolas Boy, et al.
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