Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis.

No abstract is available for this paper.

• Publication year

  2014

• Venue

  Journal of clinical neuroscience

• Publication date

  2014-11-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1016/j.jocn.2014.05.051PMID 25311418
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• [Inclusion body myositis: series of 30 cases from a Brazilian tertiary center].

  2013cited by this paper
• Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features

  2013cited by this paper
• Developing outcome measures for pediatric mitochondrial disorders: which complaints and limitations are most burdensome to patients and their parents?

  2013cited by this paper
• Pathogenic Considerations in Sporadic Inclusion-Body Myositis, a Degenerative Muscle Disease Associated With Aging and Abnormalities of Myoproteostasis

  2012cited by this paper
• Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

  2012cited by this paper
• Mitochondrial pathology in immune and inflammatory myopathies

  2010cited by this paper
• G.P.16.10 Analysis of mtDNA deletions in patients with different forms of idiopathic myositis

  2009cited by this paper
• The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders.

  2007cited by this paper
• Inclusion-body myositis

  2006cited by this paper
• Lactate increase and oxygen desaturation in mitochondrial disorders – Evaluation of two diagnostic screening protocols

  2006influential reference
• Mitochondrial abnormalities in inclusion-body myositis

  2006influential reference
• Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies.

  2005cited by this paper
• A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia.

  2003cited by this paper
• Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.

  2002cited by this paper
• A forearm exercise screening test for mitochondrial myopathy

  2002cited by this paper
• Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.

  2002cited by this paper
• Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy

  2002cited by this paper
• Disease progression in sporadic inclusion body myositis: Observations in 78 patients

  2000cited by this paper
• Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study.

  1998cited by this paper
• Intracellular phosphates in inclusion body myositis—A 31P magnetic resonance spectroscopy study

  1998cited by this paper
• Inclusion body myositis and myopathies

  1997cited by this paper
• Analysis of multiple mitochondrial DNA deletions in inclusion body myositis

  1997cited by this paper
• Cytochrome c oxidase deficiencies in the muscle of patients with inflammatory myopathies

  1996cited by this paper
• Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients

  1996cited by this paper
• Mitochondrial DNA Deletions in Muscle Fibers in Inclusion Body Myositis

  1995influential reference
• Inclusion body myositis and myopathies

  1995cited by this paper
• Mitochondrial DNA deletions in inclusion body myositis.

  1993cited by this paper
• Inclusion body myositis: analysis of 32 cases.

  1992cited by this paper
• Inclusion body myositis. Observations in 40 patients.

  1989cited by this paper

• The role of NAD+ metabolism and its modulation of mitochondria in aging and disease

  2025cites this paper
• Mitochondrial transplantation as a novel therapeutic approach in idiopathic inflammatory myopathy.

  2025cites this paper
• Mitochondrial defects in sporadic inclusion body myositis—causes and consequences

  2024cites this paper
• Secondary mitochondrial dysfunction across the spectrum of hereditary and acquired muscle disorders.

  2024cites this paper
• Oxidative stress, mitochondrial dysfunction, and respiratory chain enzyme defects in inflammatory myopathies.

  2023cites this paper
• Inhibiting de novo ceramide synthesis restores mitochondrial and protein homeostasis in muscle aging

  2023cites this paper
• Unravelling inclusion body myositis using a patient‐derived fibroblast model

  2023cites this paper
• Muscle Sonography in Inclusion Body Myositis: A Systematic Review and Meta-Analysis of 944 Measurements

  2022cites this paper
• Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis

  2021cites this paper
• NAD+ boosting reduces age-associated amyloidosis and restores mitochondrial homeostasis in muscle

  2021cites this paper
• Mitochondrial dysfunction underlying sporadic inclusion body myositis is ameliorated by the mitochondrial homing drug MA-5

  2020cites this paper
• The altered metabolism profile in pathogenesis of idiopathic inflammatory myopathies.

  2020cites this paper
• Ameliorative effect of treadmill exercise on cognitive deficits and amyloid-b pathology through the mitophagy in a mouse model of Alzheimer's disease

  2020cites this paper
• Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

  2019cites this paper
• Resistance Exercise Improves Mitochondrial Quality Control in a Rat Model of Sporadic Inclusion Body Myositis

  2019cites this paper
• The Gelsolin Pathogenic D187N Mutant Exhibits Altered Conformational Stability and Forms Amyloidogenic Oligomers.

  2018cites this paper
• Risk factors and disease mechanisms in myositis

  2018cites this paper
• Physical exercise among patients with systemic autoimmune myopathies

  2018cites this paper
• Advances in inclusion body myositis: genetics, pathogenesis and clinical aspects

  2017cites this paper
• Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis.

  2016cites this paper
• Emerging therapeutic options for sporadic inclusion body myositis

  2015cites this paper
• emerging therapeutic options for sporadic inclusion body myositis

  2015cites this paper