Cargando…

The Impact of Mitochondrial Deficiencies in Neuromuscular Diseases

Neuromuscular diseases (NMDs) are a heterogeneous group of acquired or inherited rare disorders caused by injury or dysfunction of the anterior horn cells of the spinal cord (lower motor neurons), peripheral nerves, neuromuscular junctions, or skeletal muscles leading to muscle weakness and waste. U...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cantó-Santos, Judith, Grau-Junyent, Josep M., Garrabou, Glòria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600520/ https://www.ncbi.nlm.nih.gov/pubmed/33050147 http://dx.doi.org/10.3390/antiox9100964

Ejemplares similares

Mitochondrial Dysfunction: A Common Hallmark Underlying Comorbidity between sIBM and Other Degenerative and Age-Related Diseases
por: Catalán-García, Marc, et al.
Publicado: (2020)

Neuronal induction and bioenergetics characterization of human forearm adipose stem cells from Parkinson’s disease patients and healthy controls
por: González-Casacuberta, Ingrid, et al.
Publicado: (2022)

Assessment of mitochondrial toxicity in newborns and infants with congenital cytomegalovirus infection treated with valganciclovir
por: Ortiz-Gracia, Alba, et al.
Publicado: (2022)

Editorial: Mitochondrial OXPHOS System: Emerging Concepts and Technologies and Role in Disease
por: Fernández-Vizarra, Erika, et al.
Publicado: (2022)

Integrated Multi-Omics Analysis for Inferring Molecular Players in Inclusion Body Myositis
por: Cantó-Santos, Judith, et al.
Publicado: (2023)

An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases
por: Marra, Federica, et al.
Publicado: (2021)

Mitochondrial Toxicity in Human Pregnancy: An Update on Clinical and Experimental Approaches in the Last 10 Years
por: Morén, Constanza, et al.
Publicado: (2014)

Pyruvate kinase M2 and the mitochondrial ATPase Inhibitory Factor 1 provide novel biomarkers of dermatomyositis: a metabolic link to oncogenesis
por: Santacatterina, Fulvio, et al.
Publicado: (2017)

Unravelling inclusion body myositis using a patient‐derived fibroblast model
por: Cantó‐Santos, Judith, et al.
Publicado: (2023)

Mitochondrial Mutations Can Alter Neuromuscular Transmission in Congenital Myasthenic Syndrome and Mitochondrial Disease
por: O’Connor, Kaela, et al.
Publicado: (2023)

Mitochondrial Toxicogenomics for Antiretroviral Management: HIV Post-exposure Prophylaxis in Uninfected Patients
por: Bañó, Maria, et al.
Publicado: (2020)

The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases
por: Yubero, Dèlia, et al.
Publicado: (2021)

Mitochondrial Mechanisms of Neuromuscular Junction Degeneration with Aging
por: Anagnostou, Maria-Eleni, et al.
Publicado: (2020)

The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease
por: Iyer, Shama R., et al.
Publicado: (2021)

Nutrition, Bioenergetics, and Metabolic Syndrome
por: García-García, Francesc Josep, et al.
Publicado: (2020)

The ageing neuromuscular system and sarcopenia: a mitochondrial perspective
por: Rygiel, Karolina A., et al.
Publicado: (2016)

Mitochondrial Deficiencies in the Predisposition to Paraganglioma
por: Lussey-Lepoutre, Charlotte, et al.
Publicado: (2017)

Mitochondrial and autophagic alterations in skin fibroblasts from Parkinson disease patients with Parkin mutations
por: González-Casacuberta, Ingrid, et al.
Publicado: (2019)

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study
por: Braz, Luis P., et al.
Publicado: (2021)

Exploration of SUMO2/3 Expression Levels and Autophagy Process in Fragile X-Associated Tremor/Ataxia Syndrome: Addressing Study Limitations and Insights for Future Research
por: Alvarez-Mora, Maria Isabel, et al.
Publicado: (2023)

Mitochondrial implications in human pregnancies with intrauterine growth restriction and associated cardiac remodelling
por: Guitart‐Mampel, Mariona, et al.
Publicado: (2019)

The Impact of Kinases in Amyotrophic Lateral Sclerosis at the Neuromuscular Synapse: Insights into BDNF/TrkB and PKC Signaling
por: Lanuza, Maria A., et al.
Publicado: (2019)

Subtle Neuromuscular Defects in Utrophin-deficient Mice
por: Grady, R. Mark, et al.
Publicado: (1997)

Prolonged neuromuscular block associated with cholinesterase deficiency
por: Zhang, Chao, et al.
Publicado: (2018)

Neuromuscular diseases with hypertrophic cardiomyopathy
por: Cesar, Sergi
Publicado: (2018)

Low-frequency electrotherapy for female patients with detrusor underactivity due to neuromuscular deficiency
por: Xu, Dan-Feng, et al.
Publicado: (2012)

Neuromuscular disease modeling on a chip
por: Santoso, Jeffrey W., et al.
Publicado: (2020)

Respiratory Diagnostic Tools in Neuromuscular Disease
por: Chiang, Jackie, et al.
Publicado: (2018)

Pathophysiology and Management of Fatigue in Neuromuscular Diseases
por: Torri, Francesca, et al.
Publicado: (2023)

Matrin 3 in neuromuscular disease: physiology and pathophysiology
por: Malik, Ahmed M., et al.
Publicado: (2021)

Postsynaptic Abnormalities at the Neuromuscular Junctions of Utrophin-deficient Mice
por: Deconinck, Anne E., et al.
Publicado: (1997)

Sleep Disordered Breathing in Children with Neuromuscular Disease
por: Chidambaram, Ambika G., et al.
Publicado: (2023)

Addendum: Morén, C.; Hernández, S.; Guitart-Mampel, M.; Garrabou, G. Mitochondrial Toxicity in Human Pregnancy: An Update on Clinical and Experimental Approaches in the Last 10 Years. Int. J. Environ. Res. Public Health 2014, 11, 9897–9918
por: Morén, Constanza, et al.
Publicado: (2016)

Mitochondrial response to nutrient availability and its role in metabolic disease
por: Gao, Arwen W, et al.
Publicado: (2014)

Systematic review on wearable lower-limb exoskeletons for gait training in neuromuscular impairments
por: Rodríguez-Fernández, Antonio, et al.
Publicado: (2021)

Unlocking the Complexity of Neuromuscular Diseases: Insights from Human Pluripotent Stem Cell-Derived Neuromuscular Junctions
por: Gazzola, Morgan, et al.
Publicado: (2023)

Mitochondrial toxicity and caspase activation in HIV pregnant women
por: Hernandez, Sandra, et al.
Publicado: (2016)

Molecular Insights into Mitochondrial Protein Translocation and Human Disease
por: Ruiz-Pesini, Eduardo, et al.
Publicado: (2021)

Modelling Neuromuscular Diseases in the Age of Precision Medicine
por: Speciale, Alfina A., et al.
Publicado: (2020)

AN ATLAS OF MUSCLE PATHOLOGY IN NEUROMUSCULAR DISEASES
Publicado: (1957)

Cannot write session to /tmp/vufind_sessions/sess_u6f92vo5silokvbbaags0e2ddi