Epilepsy as a pyridoxine-dependent condition: quantified urinary biomarkers for status evaluation and monitoring antiepileptic treatment.

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Medical Hypotheses

• Publication date

  2012-08-01

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1016/j.mehy.2012.04.022PMID 22647618
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)

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• Effects of levetiracetam on astroglial release of kynurenine‐pathway metabolites

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• Validation of HPLC-UV Method for Analysis of 4-Pyridoxic Acid in Human Urine

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• Epilepsy as a Pyridoxine-Dependent Condition: Quantitative Urinary Biomarkers of Epilepsy. Family Disorders of Pyridoxine Metabolism

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• Potential Contributors To The Decreased Vitamin B6 Levels After Transplantation

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• Attention-deficit hyperactivity disorder (ADHD) as a pyridoxine-dependent condition: urinary diagnostic biomarkers.

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• Substrate product ratios of enzymes in the kynurenine pathway measured in plasma as indicators of functional vitamin B-6 status.

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