Marjorie Dixon

London, ENG WC1N3JH, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

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

Single centre retrospective review of plasma branched-chain amino acid levels in children with urea cycle disorders: Impact of treatment modalities and disease severity.

Single centre retrospective review of plasma branched-chain amino acid levels in children with urea cycle disorders: Impact of treatment modalities and disease severity.

Journal: Molecular genetics and metabolism reports

Published: September 24, 2024

Asymptomatic pediatric presentation of S-adenosylhomocysteine hydrolase deficiency.

Asymptomatic pediatric presentation of S-adenosylhomocysteine hydrolase deficiency.

Journal: JIMD reports

Published: March 23, 2024

Dietary management for pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency, a follow-on from the international consortium guidelines.

Dietary management for pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency, a follow-on from the international consortium guidelines.

Journal: JIMD reports

Published: October 26, 2023

UK Dietary Practices for Tyrosinaemias: Time for Change.

UK Dietary Practices for Tyrosinaemias: Time for Change.

Journal: Nutrients

Published: October 08, 2022

BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.

BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.

Journal: Brain : a journal of neurology

Published: July 15, 2022

Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency.

Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency.

Journal: JIMD reports

Published: September 03, 2021

Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision.

Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision.

Journal: Journal of inherited metabolic disease

Published: October 10, 2020

Dietary Management, Clinical Status and Outcome of Patients with Citrin Deficiency in the UK.

Dietary Management, Clinical Status and Outcome of Patients with Citrin Deficiency in the UK.

Journal: Nutrients

Published: September 22, 2020

Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements.

Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements.

Journal: Nutrients

Published: June 17, 2020

Dietary practices in methylmalonic acidaemia: a European survey.

Dietary practices in methylmalonic acidaemia: a European survey.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: June 19, 2019

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision.

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision.

Journal: Journal of inherited metabolic disease

Published: December 07, 2018

Showing 1-12 of 16

Last Updated: 09/26/2026