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A case of pyridoxine-dependent epilepsy with novel mutations.
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Profound neonatal hypoglycemia and lactic acidosis caused by pyridoxine-dependent epilepsy.
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Pyridoxine Therapy: Not Just the Dose, the Duration Matters Too.
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Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum.
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First cases of pyridoxine-dependent epilepsy in Bulgaria: novel mutation in the ALDH7A1 gene.
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Pyridoxine-dependent epilepsy initially responsive to phenobarbital.
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Pyridoxine-dependent epilepsy: Current perspectives and questions for future research.
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Pyridoxine-Dependent Epilepsy Mimicking as Congenital Muscular Dystrophy.
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Structural analysis of pathogenic mutations targeting Glu427 of ALDH7A1, the hot spot residue of pyridoxine-dependent epilepsy.
J Inherit Metab Dis. 2020 May;43(3):635-644. doi: 10.1002/jimd.12184. Epub 2019 Dec 1.
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The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy.
J Inherit Metab Dis. 2019 Mar;42(2):353-361. doi: 10.1002/jimd.12045. Epub 2019 Feb 22.
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Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B-Dependent Epilepsy.
Am J Hum Genet. 2016 Dec 1;99(6):1325-1337. doi: 10.1016/j.ajhg.2016.10.011.
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Lysine-restricted diet and mild cerebral serotonin deficiency in a patient with pyridoxine-dependent epilepsy caused by genetic defect.
Mol Genet Metab Rep. 2014 Apr 1;1:124-128. doi: 10.1016/j.ymgmr.2014.02.001. eCollection 2014.
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Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum.
Pediatr Neurol. 2016 Jun;59:6-12. doi: 10.1016/j.pediatrneurol.2015.12.013. Epub 2016 Jan 11.
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