Yusof A. Rahman
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 18 publications
An Australian standard of care for Niemann-Pick disease type C.
Journal: Internal medicine journal
Published: November 17, 2025
Hypoglycaemia following physical exercise in a patient with novel SLC16A1 variant.
Journal: European journal of endocrinology
Published: March 16, 2024
Iridium-palladium binary alloy as a counter electrode in dye-sensitized solar cells.
Journal: Dalton transactions (Cambridge, England : 2003)
Published: November 24, 2023
Pharmacodynamics, safety, tolerability and pharmacokinetics of a single oral dose of an engineered phenylalanine ammonia-lyase in patients with phenylketonuria.
Journal: Molecular genetics and metabolism reports
Published: September 04, 2023
Diabetic ketoacidosis in an adult with beta-ketothiolase deficiency (BKD) involving a novel ACAT1 variant : first report of established diabetes in BKD and a review of the literature.
Journal: Clinical diabetes and endocrinology
Published: August 13, 2022
Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.
Journal: Journal of inherited metabolic disease
Published: March 04, 2022
GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome.
Journal: Orphanet journal of rare diseases
Published: June 19, 2021
A Retrospective Case Series Analysis of the Relationship Between Phenylalanine: Tyrosine Ratio and Cerebral Glucose Metabolism in Classical Phenylketonuria and Hyperphenylalaninemia.
Journal: Frontiers in neuroscience
Published: February 05, 2021
Clinical utilization of dried blood spot nitisinone (NTBC) and succinylacetone (SA) concentrations in hereditary tyrosinaemia type 1 - A UK centre experience.
Journal: Annals of clinical biochemistry
Published: September 16, 2020
Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients.
Journal: Orphanet journal of rare diseases
Published: September 16, 2019
Last Updated: 09/26/2026