Hyperlysinemia Latest Advances
Find the Latest Research About Hyperlysinemia
Last Updated: 06/24/2026
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Found 82 publications
Urine Metabolomics and Machine Learning Identify Metabolic Features and Potential Biomarkers of HTLV-1-Associated Myelopathy (HAM).
Journal: International journal of molecular sciences
Published: January 25, 2026
Rapid Phenotypic Screening of Lysine-Degrading Probiotics via FTIR Spectroscopy: Toward Precision Therapy for Hyperlysinemia.
Journal: ACS synthetic biology
Published: January 12, 2026
The neuropathological mechanisms underlying the inborn errors of lysine metabolism.
Journal: Neurobiology of disease
Published: November 26, 2025
Lysine α-ketoglutarate reductase as a therapeutic target for saccharopine pathway related diseases.
Journal: Frontiers in molecular neuroscience
Published: August 29, 2025
Comprehensive Review of L-Lysine: Chemistry, Occurrence, and Physiological Roles.
Journal: Current protein & peptide science
Published: January 23, 2025
New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse.
Journal: Brain communications
Published: January 21, 2025
Hyperlysinemia, an ultrarare inborn error of metabolism: Review and update.
Journal: Seizure
Published: March 25, 2024
Engineered probiotic cocktail with two cascade metabolic Escherichia coli for the treatment of hyperlysinemia.
Journal: Frontiers in microbiology
Published: January 05, 2024
A case of hyperlysinemia identified by urine newborn screening.
Journal: JIMD reports
Published: August 11, 2023
Mouse models of NADK2 deficiency analyzed for metabolic and gene expression changes to elucidate pathophysiology.
Journal: Human molecular genetics
Published: December 09, 2021
Unusual Aggregates Formed by the Self-Assembly of Proline, Hydroxyproline, and Lysine.
Journal: ACS chemical neuroscience
Published: August 18, 2021
Last Updated: 06/24/2026