Peter T. Clayton

Genetics And Genomic Medicine UCL Great Ormond Street Institute Of Child Health London UK
Strete, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 78 publications

Should PNPO Deficiency Be Treated In Utero? Clinical Findings From Prenatal Pyridoxine Therapy.

Should PNPO Deficiency Be Treated In Utero? Clinical Findings From Prenatal Pyridoxine Therapy.

Journal: JIMD reports

Published: January 22, 2026

Hepatocellular Carcinoma: A Critical Complication in Patients Treated with Pyridoxal Phosphate.

Hepatocellular Carcinoma: A Critical Complication in Patients Treated with Pyridoxal Phosphate.

Journal: Neuropediatrics

Published: December 22, 2025

Acquired vitamin B6 deficiency in POEMS: a marker of disease activity and cause of neuropathy?

Acquired vitamin B6 deficiency in POEMS: a marker of disease activity and cause of neuropathy?

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: December 21, 2025

Case report: The first report of a family with sitosterolemia in the Polish population.

Case report: The first report of a family with sitosterolemia in the Polish population.

Journal: Journal of clinical lipidology

Published: December 15, 2025

Effectiveness of Pyridoxal-5'-Phosphate in PNPO Deficiency: A Systematic Review.

Effectiveness of Pyridoxal-5'-Phosphate in PNPO Deficiency: A Systematic Review.

Journal: Journal of inherited metabolic disease

Published: May 20, 2025

Liver Transplantation in PNPO Deficiency: Management Challenges and Biological Lessons.

Liver Transplantation in PNPO Deficiency: Management Challenges and Biological Lessons.

Journal: JIMD reports

Published: May 20, 2025

Safety and efficacy analysis of in vivo lentiviral gene therapy in pre-clinical ARC syndrome models.

Safety and efficacy analysis of in vivo lentiviral gene therapy in pre-clinical ARC syndrome models.

Journal: Nature communications

Published: May 15, 2025

Treatment of Inborn Errors by Product Replacement: The Example of Inborn Errors of Bile Acid Synthesis.

Treatment of Inborn Errors by Product Replacement: The Example of Inborn Errors of Bile Acid Synthesis.

Journal: Journal of inherited metabolic disease

Published: March 26, 2025

Use of lysine reduction therapies in patients with pyridoxine dependent epilepsy due to Antiquitin deficiency - A cohort study.

Use of lysine reduction therapies in patients with pyridoxine dependent epilepsy due to Antiquitin deficiency - A cohort study.

Journal: Molecular genetics and metabolism

Published: January 29, 2025

Mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency: From metabolism to clinical implications.

Mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency: From metabolism to clinical implications.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 08, 2024

Consensus of Expert Opinion for the Diagnosis and Management of Hypermanganesaemia With Dystonia 1 and 2.

Consensus of Expert Opinion for the Diagnosis and Management of Hypermanganesaemia With Dystonia 1 and 2.

Journal: Journal of inherited metabolic disease

Published: November 11, 2024

SH-SY5Y cells undergo changes in peroxisomal metabolism when exposed to decanoic acid.

SH-SY5Y cells undergo changes in peroxisomal metabolism when exposed to decanoic acid.

Journal: Journal of neurochemistry

Published: May 02, 2024

Showing 1-12 of 78

Last Updated: 09/26/2026