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Edward Byrne
Edward Byrne
University of Melbourne, St Vincents hospital, Monash university, Institute of neurology Queen
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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
I Nishino, J Fu, K Tanji, T Yamada, S Shimojo, T Koori, M Mora, JE Riggs, ...
Nature 406 (6798), 906-910, 2000
10692000
Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing
I Trounce, E Byrne, S Marzuki
The Lancet 333 (8639), 637-639, 1989
8841989
Myostatin, insulin‐like growth factor‐1, and leukemia inhibitory factor mRNAs are upregulated in chronic human disuse muscle atrophy
KA Reardon, J Davis, RMI Kapsa, P Choong, E Byrne
Muscle & Nerve: Official Journal of the American Association of …, 2001
3292001
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, SJ Oh, M Takahashi, M Mora, ...
Neurology 58 (12), 1773-1778, 2002
2862002
Patient self-efficacy and health locus of control: relationships with health status and arthritis-related expenditure
MJ Cross, LM March, HM Lapsley, E Byrne, PM Brooks
Rheumatology 45 (1), 92-96, 2006
2352006
Respiratory chain encephalomyopathies: a diagnostic classification
UA Walker, S Collins, E Byrne
European neurology 36 (5), 260-267, 1996
2261996
The interface between metabolic and stress signalling
SJ Hey, E Byrne, NG Halford
Annals of Botany 105 (2), 197-203, 2009
2142009
Mitochondrial respiratory chain activity in the human brain as a function of age
J Ojaimi, CL Masters, K Opeskin, P McKelvie, E Byrne
Mechanisms of ageing and development 111 (1), 39-47, 1999
1771999
Quadriceps muscle wasting persists 5 months after total hip arthroplasty for osteoarthritis of the hip: a pilot study
K Reardon, M Galea, X Dennett, P Choong, E Byrne
Internal medicine journal 31 (1), 7-14, 2001
1732001
Neuroradiological features of six kindreds with MELAS tRNALeu A3243G point mutation: implications for pathogenesis
CM Sue, DS Crimmins, YS Soo, R Pamphlett, CM Presgrave, ...
Journal of Neurology, Neurosurgery & Psychiatry 65 (2), 233-240, 1998
1681998
Cochlear origin of hearing loss in MELAS syndrome
CM Sue, LJ Lipsett, DS Crimmins, CST DipAud, SC Boyages, ...
Annals of neurology 43 (3), 350-359, 1998
1591998
Isometric strength and thickness relationships in human quadriceps muscle
RJ Freilich, RLG Kirsner, E Byrne
Neuromuscular Disorders 5 (5), 415-422, 1995
1471995
Immunotherapy of ocular myasthenia gravis reduces conversion to generalized myasthenia gravis
J Mee, M Paine, E Byrne, J King, K Reardon, J O'Day
Journal of Neuro-ophthalmology 23 (4), 251-255, 2003
1262003
Reduced Collagen VI Causes Bethlem Myopathy: A Heterozygous COL6A1 Nonsense Mutation Results in mRNA Decay and Functional Haploinsufficiency
SR Lamandé, JF Bateman, W Hutchison, RJMK Gardner, SP Bower, ...
Human molecular genetics 7 (6), 981-989, 1998
1181998
In Vivo and in Vitro Correction of the mdx Dystrophin Gene Nonsense Mutation by Short-Fragment Homologous Replacement
R Kapsa, A Quigley, GS Lynch, K Steeper, AJ Kornberg, P Gregorevic, ...
Human gene therapy 12 (6), 629-642, 2001
1172001
Novel therapies for Duchenne muscular dystrophy
R Kapsa, AJ Kornberg, E Byrne
The Lancet Neurology 2 (5), 299-310, 2003
1142003
Normal variants of human mitochondrial DNA and translation products: the building of a reference data base
S Marzuki, AS Noer, P Lertrit, D Thyagarajan, R Kapsa, P Utthanaphol, ...
Human genetics 88, 139-145, 1991
1101991
Detection of MELAS A3243G point mutation in muscle, blood and hair follicles
CM Sue, A Quigley, S Katsabanis, R Kapsa, DS Crimmins, E Byrne, ...
Journal of the neurological sciences 161 (1), 36-39, 1998
1071998
Mitochondrial respiratory chain activity in idiopathic dilated cardiomyopathy
AF Quigley, RMI Kapsa, D Esmore, G Hale, E Byrne
Journal of cardiac failure 6 (1), 47-55, 2000
1042000
A tRNA (Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.
AS Noer, H Sudoyo, P Lertrit, D Thyagarajan, P Utthanaphol, R Kapsa, ...
American journal of human genetics 49 (4), 715, 1991
1011991
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