Albert Z. Lim

Newcastle Upon Tyne, ENG NE14LP, United Kingdom

Last Updated: 09/26/2026

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Found 18 publications

Advances in Primary Mitochondrial Diseases: Diagnosis, Natural History Studies and Clinical Trials.

Advances in Primary Mitochondrial Diseases: Diagnosis, Natural History Studies and Clinical Trials.

Journal: Genes
Published: June 01, 2026

Mavodelpar in patients with primary mitochondrial myopathy: a phase 1 trial.

Mavodelpar in patients with primary mitochondrial myopathy: a phase 1 trial.

Journal: Scientific reports
Published: December 11, 2025

Refractory epilepsy from lead poisoning.

Refractory epilepsy from lead poisoning.

Journal: BMJ neurology open
Published: November 19, 2025

Neurological manifestations and genotype-phenotype correlations in NDUFAF6-associated mitochondrial disease.

Neurological manifestations and genotype-phenotype correlations in NDUFAF6-associated mitochondrial disease.

Journal: Brain communications
Published: July 25, 2025

Adjunctive transcranial DC stimulation in the management of refractory drug-resistant focal epilepsy in POLG mitochondrial disease: A case series.

Adjunctive transcranial DC stimulation in the management of refractory drug-resistant focal epilepsy in POLG mitochondrial disease: A case series.

Journal: Seizure
Published: April 14, 2025

TRANscranial direct current stimulation for FOcal Refractory epilepsy in mitochondrial disease (TRANSFORM): delayed-start, randomised, double-blinded, placebo-controlled study.

TRANscranial direct current stimulation for FOcal Refractory epilepsy in mitochondrial disease (TRANSFORM): delayed-start, randomised, double-blinded, placebo-controlled study.

Journal: BMC neurology
Published: June 28, 2024

Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease.

Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease.

Journal: JCI insight
Published: December 19, 2023

Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus.

Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus.

Journal: Child neurology open
Published: April 08, 2023

Endocrine Manifestations and New Developments in Mitochondrial Disease.

Endocrine Manifestations and New Developments in Mitochondrial Disease.

Journal: Endocrine reviews
Published: June 01, 2021

Natural History of Leigh Syndrome: A Study of Disease Burden and Progression.

Natural History of Leigh Syndrome: A Study of Disease Burden and Progression.

Journal: Annals of neurology
Published: March 31, 2021

Current and Emerging Clinical Treatment in Mitochondrial Disease.

Current and Emerging Clinical Treatment in Mitochondrial Disease.

Journal: Molecular diagnosis & therapy
Published: December 27, 2020

A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features.

A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features.

Journal: Neuromuscular disorders : NMD
Published: January 09, 2020
Showing 1-12 of 18

Last Updated: 09/26/2026