On the public citation graph
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations
0 signed · 83 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ana.22095openalex-snapshot
Use of guidelines improves the neurological outcome in glutaric aciduria type I
inferredcites →https://doi.org/10.1002/ana.24027openalex-snapshot
Glial localization of antiquitin: Implications for pyridoxine‐dependent epilepsy
inferredcites →https://doi.org/10.1007/bf01958419openalex-snapshot
Pyridoxine-dependent seizures, clinical and therapeutic aspects
inferredcites →https://doi.org/10.1007/s00431-008-0823-xopenalex-snapshot
Clinical features and the management of pyridoxine-dependent and pyridoxine-responsive seizures: review of 63 North American cases submitted to a patient registry
inferredcites →https://doi.org/10.1007/s10545-011-9289-5openalex-snapshot
Diagnosis and management of glutaric aciduria type I – revised recommendations
inferredcites →https://doi.org/10.1007/s10545-012-9455-4openalex-snapshot
Cultural aspects in the management of inborn errors of metabolism
inferredcites →https://doi.org/10.1007/s10545-012-9466-1openalex-snapshot
Urinary AASA excretion is elevated in patients with molybdenum cofactor deficiency and isolated sulphite oxidase deficiency
inferredcites →https://doi.org/10.1007/s10545-012-9493-yopenalex-snapshot
Measurement of plasma B6 vitamer profiles in children with inborn errors of vitamin B6 metabolism using an LC‐MS/MS method
inferredcites →https://doi.org/10.1016/j.ymgme.2011.05.014openalex-snapshot
Pyridoxine dependent epilepsy and antiquitin deficiency
inferredcites →https://doi.org/10.1016/j.ymgme.2011.07.003openalex-snapshot
Safety, efficacy and physiological actions of a lysine-free, arginine-rich formula to treat glutaryl-CoA dehydrogenase deficiency: Focus on cerebral amino acid influx
inferredcites →https://doi.org/10.1016/j.ymgme.2012.03.021openalex-snapshot
Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience
inferredcites →https://doi.org/10.1016/j.ymgme.2012.09.006openalex-snapshot
Lysine restricted diet for pyridoxine-dependent epilepsy: First evidence and future trials
inferredcites →https://doi.org/10.1016/j.ymgme.2013.04.018openalex-snapshot
Normal plasma pipecolic acid level in pyridoxine dependent epilepsy due to ALDH7A1 mutations
inferredcites →https://doi.org/10.1016/j.ymgme.2013.07.017openalex-snapshot
Preliminary investigation of the use of newborn dried blood spots for screening pyridoxine-dependent epilepsy by LC-MS/MS
inferredcites →https://doi.org/10.1017/s0007114599000082openalex-snapshot
Non-nutritional uses of vitamin B6
inferredcites →https://doi.org/10.1017/s0012162201000779openalex-snapshot
Pyridoxine-dependent and pyridoxine-responsive seizures
inferredcites →https://doi.org/10.1038/nm1366openalex-snapshot
Mutations in antiquitin in individuals with pyridoxine-dependent seizures
inferredcites →https://doi.org/10.1093/brain/awq143openalex-snapshot
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)
inferredcites →https://doi.org/10.1111/j.1469-8749.2012.04347.xopenalex-snapshot
Long‐term outcome in pyridoxine‐dependent epilepsy
inferredcites →https://doi.org/10.1111/j.1469-8749.2012.04354.xopenalex-snapshot
Natural history of pyridoxine‐dependent epilepsy: tools for prognostication
inferredcites →https://doi.org/10.1136/fn.81.2.f125openalex-snapshot
Pyridoxine dependent epilepsy: a suggestive electroclinical pattern
inferredcites →https://doi.org/10.1203/01.pdr.0000219387.79887.86openalex-snapshot
Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency
inferredcites →https://doi.org/10.4324/9780429036279-4openalex-snapshot
Energy and protein requirements*
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4585169openalex-extracted
Partial Suppression of Bcaa Catabolism as a Potential Therapy for Bckdk Deficiency
inferred← citeshttps://doi.org/10.2139/ssrn.4670032openalex-extracted
Partial Suppression of BCAA Catabolism as a Potential Therapy for BCKDK Deficiency
inferred← citeshttps://doi.org/10.1002/ajmg.a.61815openalex-snapshot
A cautionary tale of pyridoxine toxicity in cystathionine beta‐synthase deficiency detected by two‐tier newborn screening highlights the need for clear pyridoxine dosing guidelines
inferred← citeshttps://doi.org/10.1002/cns3.20016openalex-snapshot
Pyridoxine‐dependent epilepsy: Current perspectives and questions for future research
inferred← citeshttps://doi.org/10.1002/jimd.12233openalex-snapshot
Impact of enteral arginine supplementation on lysine metabolism in humans: A proof‐of‐concept for lysine‐related inborn errors of metabolism
inferred← citeshttps://doi.org/10.1002/jimd.12332openalex-snapshot
Consensus guidelines for the diagnosis and management of pyridoxine‐dependent epilepsy due to α‐aminoadipic semialdehyde dehydrogenase deficiency
inferred← citeshttps://doi.org/10.1002/jmd2.12418openalex-snapshot
Dietary management for pyridoxine‐dependent epilepsy due to α‐aminoadipic semialdehyde dehydrogenase deficiency, a follow‐on from the international consortium guidelines
inferred← citeshttps://doi.org/10.1002/mgg3.355openalex-snapshot
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
inferred← citeshttps://doi.org/10.1007/978-3-030-02992-0_3openalex-snapshot
Medical Issues, Therapies, and Treatments
inferred← citeshttps://doi.org/10.1007/978-3-030-67727-5_34openalex-snapshot
Vitamin B6-Dependent and Vitamin B6-Responsive Disorders
inferred← citeshttps://doi.org/10.1007/978-3-662-43751-3openalex-snapshot
JIMD Reports - Case and Research Reports, Volume 15
inferred← citeshttps://doi.org/10.1007/s11011-016-9869-zopenalex-snapshot
Pyridoxine-dependent epilepsy: report on three families with neuropathology
inferred← citeshttps://doi.org/10.1007/s11011-016-9933-8openalex-snapshot
Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy
inferred← citeshttps://doi.org/10.1007/s11940-014-0335-0openalex-snapshot
Current Treatment and Management of Pyridoxine-Dependent Epilepsy
inferred← citeshttps://doi.org/10.1007/s13760-020-01467-3openalex-snapshot
Clinical and biochemical outcome of a patient with pyridoxine-dependent epilepsy treated by triple therapy (pyridoxine supplementation, lysine-restricted diet, and arginine supplementation)
inferred← citeshttps://doi.org/10.1016/b978-0-12-410529-4.00049-8openalex-snapshot
Disorders of Pyridoxine Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-813955-4.00053-2openalex-snapshot
Disorders of pyridoxine metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-443-19176-3.00062-5openalex-snapshot
Disorders of pyridoxine metabolism
inferred← citeshttps://doi.org/10.1016/j.cdnut.2025.107504openalex-snapshot
Combination Therapy with Pyridoxine and Arginine Supplementations along with a Lysine-Restricted Diet in Individuals with Pyridoxine-Dependent Epilepsy: A Comprehensive Systematic Review
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115069openalex-snapshot
Restricting lysine normalizes toxic catabolites associated with ALDH7A1 deficiency in cells and mice
inferred← citeshttps://doi.org/10.1016/j.ejpn.2015.08.001openalex-snapshot
Long-term outcome in pyridoxine-responsive infantile epilepsy
inferred← citeshttps://doi.org/10.1016/j.ejpn.2021.06.001openalex-snapshot
Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2025.107511openalex-snapshot
Restoring tigecycline efficacy with lysine supplementation in tmexCD-toprJ-positive bacteria
inferred← citeshttps://doi.org/10.1016/j.jchromb.2016.02.043openalex-snapshot
A novel method for simultaneous quantification of alpha-aminoadipic semialdehyde/piperideine-6-carboxylate and pipecolic acid in plasma and urine
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2020.06.010openalex-snapshot
Seizing the moment: Zebrafish epilepsy models
inferred← citeshttps://doi.org/10.1016/j.pediatrneurol.2015.12.013openalex-snapshot
Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum
inferred← citeshttps://doi.org/10.1016/j.pediatrneurol.2016.03.008openalex-snapshot
A Prospective Case Study of the Safety and Efficacy of Lysine-Restricted Diet and Arginine Supplementation Therapy in a Patient With Pyridoxine-Dependent Epilepsy Caused by Mutations in ALDH7A1
inferred← citeshttps://doi.org/10.1016/j.spen.2016.06.004openalex-snapshot
Amenable Treatable Severe Pediatric Epilepsies
inferred← citeshttps://doi.org/10.1016/j.spen.2025.101204openalex-snapshot
Genetic testing for infantile-onset epilepsies in resource-limited settings
inferred← citeshttps://doi.org/10.1016/j.yebeh.2023.109363openalex-snapshot
Update current understanding of neurometabolic disorders related to lysine metabolism
inferred← citeshttps://doi.org/10.1016/j.ymgme.2015.03.001openalex-snapshot
Retrospective analysis supports algorithm as efficient diagnostic approach to treatable intellectual developmental disabilities
inferred← citeshttps://doi.org/10.1016/j.ymgme.2015.05.011openalex-snapshot
Triple therapy with pyridoxine, arginine supplementation and dietary lysine restriction in pyridoxine-dependent epilepsy: Neurodevelopmental outcome
inferred← citeshttps://doi.org/10.1016/j.ymgme.2015.12.007openalex-snapshot
Metabolic Diet App Suite for inborn errors of amino acid metabolism
inferred← citeshttps://doi.org/10.1016/j.ymgme.2016.04.015openalex-snapshot
Effect of dietary lysine restriction and arginine supplementation in two patients with pyridoxine-dependent epilepsy
inferred← citeshttps://doi.org/10.1016/j.ymgmr.2024.101091openalex-snapshot
Partial suppression of BCAA catabolism as a potential therapy for BCKDK deficiency
inferred← citeshttps://doi.org/10.1021/acssynbio.5c00725openalex-snapshot
Rapid Phenotypic Screening of Lysine-Degrading Probiotics via FTIR Spectroscopy: Toward Precision Therapy for Hyperlysinemia
inferred← citeshttps://doi.org/10.1055/s-0037-1621721openalex-snapshot
Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings
inferred← citeshttps://doi.org/10.1055/s-0045-1808381openalex-snapshot
Status epilepticus nach Asphyxie als diagnostische Herausforderung: Antiquitin-Mangel als seltene Differentialdiagnose
inferred← citeshttps://doi.org/10.1080/14737175.2019.1648212openalex-snapshot
Update on the treatment of vitamin B6 dependent epilepsies
inferred← citeshttps://doi.org/10.1080/14737175.2021.1885374openalex-snapshot
Managing CLN2 disease: a treatable neurodegenerative condition among other treatable early childhood epilepsies
inferred← citeshttps://doi.org/10.1080/17446651.2017.1273107openalex-snapshot
Current knowledge for pyridoxine-dependent epilepsy: a 2016 update
inferred← citeshttps://doi.org/10.1080/23808993.2018.1486189openalex-snapshot
Personalized treatment in the epilepsies: challenges and opportunities
inferred← citeshttps://doi.org/10.1093/hmg/ddaa202openalex-snapshot
A novel mouse model for pyridoxine-dependent epilepsy due to antiquitin deficiency
inferred← citeshttps://doi.org/10.1101/2024.09.03.24312979openalex-snapshot
Evaluating whole genome sequencing for rare diseases in newborn screening: evidence synthesis from a series of systematic reviews
inferred← citeshttps://doi.org/10.1101/mcs.a006197openalex-snapshot
A case for newborn screening for pyridoxine-dependent epilepsy
inferred← citeshttps://doi.org/10.1111/epi.16408openalex-snapshot
Diagnosis of pyridoxine‐dependent epilepsy in an adult presenting with recurrent status epilepticus
inferred← citeshttps://doi.org/10.1155/2019/2893041openalex-snapshot
Metagenomics and Faecal Metabolomics Integrative Analysis towards the Impaired Glucose Regulation and Type 2 Diabetes in Uyghur-Related Omics
inferred← citeshttps://doi.org/10.1186/s12883-024-03936-1openalex-snapshot
Pyridoxine-dependent epilepsy caused by an ALDH7A1 mutation in an infant girl: the first case report in Syria
inferred← citeshttps://doi.org/10.1212/wnl.0000000000005748openalex-snapshot
Geometric morphometrics reveal altered corpus callosum shape in pyridoxine-dependent epilepsy
inferred← citeshttps://doi.org/10.1212/wnl.0000000000201222openalex-snapshot
Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy
inferred← citeshttps://doi.org/10.1371/journal.pone.0186645openalex-snapshot
Characterization of the first knock-out aldh7a1 zebrafish model for pyridoxine-dependent epilepsy using CRISPR-Cas9 technology
inferred← citeshttps://doi.org/10.15761/ndt.1000109openalex-snapshot
Refractory seizures in a term neonate due to pyridoxine dependent epilepsy
inferred← citeshttps://doi.org/10.20966/chn.2016.51.385openalex-snapshot
Current diagnosis and treatment of pyridoxine dependent epilepsy due to antiqutin deficiency
inferred← citeshttps://doi.org/10.2174/011573398x289178240528052344openalex-snapshot
Respiratory Complications in the Inborn Errors of Metabolism
inferred← citeshttps://doi.org/10.26815/acn.2022.00122openalex-snapshot
A Patient with Pyridoxine-Dependent Epilepsy Who Was Treated with Triple Therapy
inferred← citeshttps://doi.org/10.3390/brainsci12010065openalex-snapshot
Pyridoxine-Dependent Epilepsy and Antiquitin Deficiency Resulting in Neonatal-Onset Refractory Seizures
inferred← citeshttps://doi.org/10.3410/f.732440288.793555817openalex-snapshot
Faculty Opinions recommendation of Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness.
inferred← citeshttps://doi.org/10.4103/aian.aian_204_19openalex-snapshot
Pyridoxine trial in early infantile epileptic encephalopathy: Never forget!
inferred← citeshttps://doi.org/10.4103/jpn.jpn_160_16openalex-snapshot
Actual insights into treatable inborn errors of metabolism causing epilepsy
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.