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Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S23-S23

2017

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P53 Novel SDHA and SDHB mutations as a cause of isolated mitochondrial complex II deficiency

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S21-S21

2012

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Disease progression in patients with single, large-scale mitochondrial DNA deletions

Brain (London, England : 1878), 2014-02, Vol.137 (Pt 2), p.323-334

2014

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Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease

Human molecular genetics, 2022-06, Vol.31 (12), p.2049-2062

2022

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P62 Long term endurance training and deconditioning in patients with mitochondrial myopathy

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S24-S24

2012

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P61 Resistance training in patients with mitochondrial myopathy

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S23-S24

2012

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M20 - Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S23-S23

2017

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Quantitative 3D mapping of the skeletal muscle mitochondrial network in health and mtDNA disease

Neuromuscular disorders : NMD, 2018-04, Vol.28, p.S34

2018

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M15 - Quantitative 3D mapping of the skeletal muscle mitochondrial network in health and mtDNA disease

Neuromuscular disorders : NMD, 2018-04, Vol.28, p.S34-S34

2018

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Clonally expanded mtDNA deletions in human skeletal muscle originate as a proliferative perinuclear niche

Neuromuscular disorders : NMD, 2018-04, Vol.28, p.S34-S35

2018

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M16 - Clonally expanded mtDNA deletions in human skeletal muscle originate as a proliferative perinuclear niche

Neuromuscular disorders : NMD, 2018-04, Vol.28, p.S34-S35

2018

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Oxidative damage to protein in sporadic motor neuron disease spinal cord

Annals of neurology, 1995-10, Vol.38 (4), p.691-695

1995

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Comparison of cathepsin protease activities in brain tissue from normal cases and cases with Alzheimer's disease, Lewy body dementia, Parkinson's disease and Huntington's disease

Journal of the neurological sciences, 1995-07, Vol.131 (1), p.65-70

1995

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Quantification of protease activities in synovial fluid from rheumatoid and osteoarthritis cases: comparison with antioxidant and free radical damage markers

Clinica chimica acta, 1999-06, Vol.284 (1), p.45-58

1999

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Cytoplasmic, lysosomal and matrix protease activities in spinal cord tissue from amyotrophic lateral sclerosis (ALS) and control patients

Journal of the neurological sciences, 1996-08, Vol.139 (suppl), p.71-75

1996

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Cerebellar ataxia in coeliac disease--no evidence of a humoral aetiology

Postgraduate medical journal, 1995-03, Vol.71 (833), p.186-186

1995

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Oxidants, antioxidants and alcohol: implications for skeletal and cardiac muscle

Frontiers in bioscience, 1999, Vol.4 (5), p.e58-66, Article A480

1999

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Effect of growth promoters on pig muscle structural protein and proteolytic enzyme levels in vivo and in vitro

Biochimie, 1993, Vol.75 (10), p.839-847

1993

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Comparison of methods for determination of total antioxidant status: application to analysis of medicinal plant essential oils

Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 1998-12, Vol.121 (4), p.385-391

1998

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Dystrophin or a "related protein" in Duchenne muscular dystrophy?

Acta neurologica Scandinavica, 1992-07, Vol.86 (1), p.8-14

1992

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Comparison of proline endopeptidase activity in brain tissue from normal cases and cases with Alzheimer's disease, Lewy body dementia, Parkinson's disease and Huntington's disease

Clinica chimica acta, 1996-05, Vol.249 (1), p.129-139

1996

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Skeletal muscle protein loss due to D-penicillamine results from reduced protein synthesis

The international journal of biochemistry & cell biology, 2001-10, Vol.33 (10), p.1013-1026

2001

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Carbonyl Levels in Type I and II Fiber-Rich Muscles and Their Response to Chronic Ethanol Feeding In Vivo and Hydroxyl and Superoxide Radicals In Vitro

Alcoholism, clinical and experimental research, 2000-12, Vol.24 (12), p.1862-1868

2000

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Dystrophin in skeletal muscle I. Western blot analysis using a monoclonal antibody

Journal of the neurological sciences, 1989-12, Vol.94 (1), p.125-136

1989

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Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

P53 Novel SDHA and SDHB mutations as a cause of isolated mitochondrial complex II deficiency

Disease progression in patients with single, large-scale mitochondrial DNA deletions

Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability

Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease

P62 Long term endurance training and deconditioning in patients with mitochondrial myopathy

P61 Resistance training in patients with mitochondrial myopathy

M20 - Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

Quantitative 3D mapping of the skeletal muscle mitochondrial network in health and mtDNA disease

M15 - Quantitative 3D mapping of the skeletal muscle mitochondrial network in health and mtDNA disease

Clonally expanded mtDNA deletions in human skeletal muscle originate as a proliferative perinuclear niche

M16 - Clonally expanded mtDNA deletions in human skeletal muscle originate as a proliferative perinuclear niche

Oxidative damage to protein in sporadic motor neuron disease spinal cord

Comparison of cathepsin protease activities in brain tissue from normal cases and cases with Alzheimer's disease, Lewy body dementia, Parkinson's disease and Huntington's disease

Quantification of protease activities in synovial fluid from rheumatoid and osteoarthritis cases: comparison with antioxidant and free radical damage markers

Cytoplasmic, lysosomal and matrix protease activities in spinal cord tissue from amyotrophic lateral sclerosis (ALS) and control patients

Cerebellar ataxia in coeliac disease--no evidence of a humoral aetiology

Oxidants, antioxidants and alcohol: implications for skeletal and cardiac muscle

Effect of growth promoters on pig muscle structural protein and proteolytic enzyme levels in vivo and in vitro

Comparison of methods for determination of total antioxidant status: application to analysis of medicinal plant essential oils

Dystrophin or a "related protein" in Duchenne muscular dystrophy?

Comparison of proline endopeptidase activity in brain tissue from normal cases and cases with Alzheimer's disease, Lewy body dementia, Parkinson's disease and Huntington's disease

Skeletal muscle protein loss due to D-penicillamine results from reduced protein synthesis

Carbonyl Levels in Type I and II Fiber-Rich Muscles and Their Response to Chronic Ethanol Feeding In Vivo and Hydroxyl and Superoxide Radicals In Vitro

Dystrophin in skeletal muscle I. Western blot analysis using a monoclonal antibody

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