Hugh A. Lemonde
Westminster Bridge Rd
London, ENG SE17EH, United Kingdom
London, ENG SE17EH, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Blood Phenylalanine Control in Paediatric and Adult Centres in the UK: Data from 2012-2018.
Journal: Nutrients
Published: May 11, 2026
Reduced and Personalized Fasting Regimens to Avoid Metabolic Complications in Pediatric Anesthesia.
Journal: Paediatric anaesthesia
Published: March 28, 2026
From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D-Bifunctional Protein Deficiency in a Multicentre International Case Series.
Journal: Journal of inherited metabolic disease
Published: September 24, 2025
Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non-Finnish Patients.
Journal: American journal of medical genetics. Part A
Published: May 15, 2025
Early postnatal hepatocyte transplantation in a child with molybdenum cofactor deficiency type B.
Journal: Molecular genetics and metabolism
Published: January 14, 2025
Retrospective Review of Positive Newborn Screening Results for Isovaleric Acidemia and Development of a Strategy to Improve the Efficacy of Newborn Screening in the UK.
Journal: International journal of neonatal screening
Published: January 23, 2024
Liver transplantation in ornithine transcarbamylase deficiency: A retrospective multicentre cohort study.
Journal: Molecular genetics and metabolism reports
Published: November 01, 2023
Performance of laboratory tests used to measure blood phenylalanine for the monitoring of patients with phenylketonuria.
Journal: Journal of inherited metabolic disease
Published: March 07, 2019
Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency.
Journal: American journal of human genetics
Published: May 01, 2018
An infant and mother with severe B12 deficiency: vitamin B12 status assessment should be determined in pregnant women with anaemia.
Journal: European journal of clinical nutrition
Published: January 23, 2017
A new method for the rapid diagnosis of protein N-linked congenital disorders of glycosylation.
Journal: Journal of proteome research
Published: June 08, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026