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Albert Lim
Albert Lim
Paediatric neurology doctor and researcher
Verified email at newcastle.ac.uk
Title
Cited by
Cited by
Year
Current and emerging clinical treatment in mitochondrial disease
RJ Tinker, AZ Lim, RJ Stefanetti, R McFarland
Molecular diagnosis & therapy 25, 181-206, 2021
572021
The mitochondrial epilepsies
A Lim, RH Thomas
European journal of paediatric neurology 24, 47-52, 2020
542020
Resolving complexity in mitochondrial disease: Towards precision medicine
RM Boggan, A Lim, RW Taylor, R McFarland, SJ Pickett
Molecular genetics and metabolism 128 (1-2), 19-29, 2019
412019
Pathogenic variants in MT‐ATP6: A United Kingdom–based mitochondrial disease cohort study
YS Ng, MH Martikainen, GS Gorman, A Blain, E Bugiardini, A Bunting, ...
Annals of neurology 86 (2), 310-315, 2019
412019
Epidemiology of mitochondrial disease
A Schaefer, A Lim, G Gorman
Diagnosis and management of mitochondrial disorders, 63-79, 2019
302019
Kikuchi-Fujimoto disease: a case report and literature review
V Veer, A Lim, W Issing
Case reports in Otolaryngology 2012, 2012
302012
A case‐comparison study of pregnant women with mitochondrial disease–what to expect?
CL Feeney, AZ Lim, E Fagan, A Blain, A Bright, J Maddison, H Devine, ...
BJOG: An International Journal of Obstetrics & Gynaecology 126 (11), 1380-1389, 2019
212019
Endocrine manifestations and new developments in mitochondrial disease
YS Ng, AZ Lim, G Panagiotou, DM Turnbull, M Walker
Endocrine reviews 43 (3), 583-609, 2022
192022
Natural history of Leigh syndrome: a study of disease burden and progression
AZ Lim, YS Ng, A Blain, C Jiminez‐Moreno, CL Alston, V Nesbitt, ...
Annals of Neurology 91 (1), 117-130, 2022
192022
Diagnosis and management of mitochondrial disorders
M Mancuso, T Klopstock
Springer, 2019
162019
Diagnosing pediatric mitochondrial disease: lessons from 2,000 exomes
SL Stenton, M Shimura, D Piekutowska-Abramczuk, P Freisinger, ...
medRxiv, 2021.06. 21.21259171, 2021
122021
A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features
AZ Lim, G McMacken, F Rastelli, M Oláhová, K Baty, S Hopton, G Falkous, ...
Neuromuscular Disorders 30 (8), 661-668, 2020
92020
RRM2B mitochondrial DNA maintenance defects
AZ Lim, R McFarland, RW Taylor, GS Gorman
82021
Risk of cardiac manifestations in adult mitochondrial disease caused by nuclear genetic defects
AZ Lim, DM Jones, MGD Bates, AM Schaefer, J O'Sullivan, C Feeney, ...
Open Heart 8 (1), e001510, 2021
42021
A novel pathogenic m. 4412G> A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes
AZ Lim, EL Blakely, K Baty, L He, S Hopton, G Falkous, K McWilliam, ...
Mitochondrion 47, 18-23, 2019
32019
Leigh Syndrome
AZ Lim, R McFarland
Diagnosis and Management of Mitochondrial Disorders, 151-167, 2019
22019
Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus
M Khries, A Lim, D Mitra, M Anderson, J Bengtsson, A Bowron, E Harris, ...
Child Neurology Open 10, 2329048X231184183, 2023
12023
Factors associated with the severity of COVID‐19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID‐19 Registry
C Pizzamiglio, RDS Pitceathly, MP Lunn, S Brady, F De Marchi, L Galan, ...
European Journal of Neurology 30 (2), 399-412, 2023
12023
P20 Impact on mode of delivery and early neonatal outcomes following fetal diagnosis of life-threatening congenital heart disease in the north east of england
A Lim, P Moran, M Kontou, WNW Montil, M Abu-Harb, A McBrien
Heart 102 (Suppl 1), A11-A11, 2016
12016
449 Improving the care of neurosurgical patients: a new teaching model for paediatric trainees
C Angus, H Van Ruiten, A Lim, I Coulter
Archives of Disease in Childhood 108 (Suppl 2), A409-A410, 2023
2023
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Articles 1–20