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Gallagher RC
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Triple therapy with pyridoxine, arginine supplementation and dietary lysine restriction in pyridoxine-dependent epilepsy: Neurodevelopmental outcome
Clinical and biochemical characterization of four patients with mutations in ECHS1
Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations
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