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Coenzyme Q10 and Autoimmune Disorders: An Overview

International journal of molecular sciences, 2024-04, Vol.25 (8), p.4576

2024

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Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

Cell metabolism, 2013-06, Vol.17 (6), p.941-953

2013

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Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases

International journal of molecular sciences, 2021-10, Vol.22 (21), p.11444

2021

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Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

Neurobiology of aging, 2014-05, Vol.35 (5), p.1111-1115

2014

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The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells

Journal of neurochemistry, 2014-05, Vol.129 (3), p.426-433

2014

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Coenzyme Q10 in Mitochondrial and Lysosomal Disorders

Journal of clinical medicine, 2021-05, Vol.10 (9), p.1970

Hargreaves, Iain P.

2021

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Coenzyme Q10: Role in Less Common Age-Related Disorders

Antioxidants, 2022-11, Vol.11 (11), p.2293

2022

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Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10573

2022

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Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis

International journal of molecular sciences, 2019-10, Vol.20 (20), p.4975

2019

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Coenzyme Q10 and Immune Function: An Overview

Antioxidants, 2021-05, Vol.10 (5), p.759

2021

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Evidence of Oxidative Stress and Secondary Mitochondrial Dysfunction in Metabolic and Non-Metabolic Disorders

Journal of clinical medicine, 2017-07, Vol.6 (7), p.71

2017

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Depletion and Supplementation of Coenzyme Q10 in Secondary Deficiency Disorders

Frontiers in bioscience (Landmark. Print), 2022-12, Vol.27 (12), p.322-322

2022

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Primary Coenzyme Q10 Deficiency: An Update

Antioxidants, 2023-08, Vol.12 (8), p.1652

2023

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A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

American journal of human genetics, 2009-05, Vol.84 (5), p.558-566

2009

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Coenzyme Q10, Ageing and the Nervous System: An Overview

Antioxidants, 2021-12, Vol.11 (1), p.2

2021

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The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q10 Status and Mitochondrial Function

International journal of molecular sciences, 2020-11, Vol.21 (23), p.9137

2020

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Current Strategies for the Biochemical Diagnosis and Monitoring of Mitochondrial Disease

Hargreaves, Iain

2018

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Lyme Disease: A Role for Coenzyme Q10 Supplementation?

Antioxidants, 2022-03, Vol.11 (4), p.667

2022

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ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Journal of neurology, 2014-11, Vol.261 (11), p.2192-2198

2014

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Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats

Disease models & mechanisms, 2016-10, Vol.9 (10), p.1221-1229

2016

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Mitochondrial dysfunction is a key pathological driver of early stage Parkinson's

Acta neuropathologica communications, 2022-09, Vol.10 (1), p.134-134, Article 134

2022

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Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment

Journal of inherited metabolic disease, 2013-01, Vol.36 (1), p.63-73

2013

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Potential Biomarkers of Mitochondrial Dysfunction Associated with COVID-19 Infection

Advances in experimental medicine and biology, 2023, Vol.1412, p.211-224

2023

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Biochemical Assessment and Monitoring of Mitochondrial Disease

Journal of clinical medicine, 2018-03, Vol.7 (4), p.66

Hargreaves, Iain P

2018

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Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma

International journal of molecular sciences, 2019-07, Vol.20 (13), p.3364

2019

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Coenzyme Q10 and Autoimmune Disorders: An Overview

Mitochondria and Quality Control Defects in a Mouse Model of Gaucher Disease—Links to Parkinson’s Disease

Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases

Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells

Coenzyme Q10 in Mitochondrial and Lysosomal Disorders

Coenzyme Q10: Role in Less Common Age-Related Disorders

Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies

Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis

Coenzyme Q10 and Immune Function: An Overview

Evidence of Oxidative Stress and Secondary Mitochondrial Dysfunction in Metabolic and Non-Metabolic Disorders

Depletion and Supplementation of Coenzyme Q10 in Secondary Deficiency Disorders

Primary Coenzyme Q10 Deficiency: An Update

A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease

Coenzyme Q10, Ageing and the Nervous System: An Overview

The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q10 Status and Mitochondrial Function

Current Strategies for the Biochemical Diagnosis and Monitoring of Mitochondrial Disease

Lyme Disease: A Role for Coenzyme Q10 Supplementation?

ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Poor maternal nutrition and accelerated postnatal growth induces an accelerated aging phenotype and oxidative stress in skeletal muscle of male rats

Mitochondrial dysfunction is a key pathological driver of early stage Parkinson's

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment

Potential Biomarkers of Mitochondrial Dysfunction Associated with COVID-19 Infection

Biochemical Assessment and Monitoring of Mitochondrial Disease

Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma

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