Cargando…

COVID-19–Related Outcomes in Primary Mitochondrial Diseases: An International Study

BACKGROUND AND OBJECTIVES: To identify factors associated with severe coronavirus disease 2019 (COVID-19), defined by hospitalization status, in patients with primary mitochondrial diseases (PMDs), thereby enabling future risk stratification and informed management decisions. METHODS: We undertook a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pizzamiglio, Chiara, Machado, Pedro M., Thomas, Rhys H., Gorman, Gráinne S., McFarland, Robert, Hanna, Michael G., Pitceathly, Robert D. S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Clinical/Scientific Note
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992603/ https://www.ncbi.nlm.nih.gov/pubmed/35190464 http://dx.doi.org/10.1212/WNL.0000000000200240

Ejemplares similares

Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes
por: Pizzamiglio, Chiara, et al.
Publicado: (2021)

Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant
por: Poole, Olivia V., et al.
Publicado: (2020)

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy
por: Hardy, Steven A., et al.
Publicado: (2016)

Safety of drug use in patients with a primary mitochondrial disease: An international Delphi‐based consensus
por: De Vries, Maaike C., et al.
Publicado: (2020)

Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia
por: Sommerville, Ewen W., et al.
Publicado: (2017)

Scientific and Ethical Issues in Mitochondrial Donation
por: Craven, Lyndsey, et al.
Publicado: (2018)

Mitochondrial Strokes: Diagnostic Challenges and Chameleons
por: Pizzamiglio, Chiara, et al.
Publicado: (2021)

Spinocerebellar ataxia type 10 in Chinese Han
por: Wang, Kang, et al.
Publicado: (2015)

Height as a Clinical Biomarker of Disease Burden in Adult Mitochondrial Disease
por: Boal, Rachel L, et al.
Publicado: (2018)

l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes: A Systematic Review
por: Stefanetti, Renae J., et al.
Publicado: (2022)

Perceived fatigue is highly prevalent and debilitating in patients with mitochondrial disease
por: Gorman, Gráinne S., et al.
Publicado: (2015)

Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha–Related Diseases
por: Primiano, Guido, et al.
Publicado: (2022)

Preliminary Evaluation of Clinician Rated Outcome Measures in Mitochondrial Disease
por: Newman, Jane, et al.
Publicado: (2015)

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy
por: Dombi, Eszter, et al.
Publicado: (2016)

MRI Features and Their Association With Outcomes in Children With Anti-NMDA Receptor Encephalitis
por: Gombolay, Grace, et al.
Publicado: (2023)

Unilateral Relapsing Primary CNS Vasculitis: Description of 3 Cases From a Single-Institutional Cohort of 216 Cases
por: Salvarani, Carlo, et al.
Publicado: (2023)

The rare case of a 20-year-old male with rapidly progressive primary angiitis of the CNS with a good outcome
por: Graham, Edith, et al.
Publicado: (2020)

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
por: Gorman, Gráinne S., et al.
Publicado: (2015)

Consensus-based statements for the management of mitochondrial stroke-like episodes
por: Ng, Yi Shiau, et al.
Publicado: (2019)

Refractory IgG4-related intracranial hypertrophic pachymeningitis responded to rituximab
por: Liao, Bing, et al.
Publicado: (2014)

Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome
por: Veerapandiyan, Aravindhan, et al.
Publicado: (2016)

Deoxyguanosine kinase mutation producing juvenile-onset mitochondrial myopathy
por: Komal, F.N.U., et al.
Publicado: (2018)

Mitochondrial cerebellar ataxia, renal failure, neuropathy, and encephalopathy (MCARNE)
por: Ng, Peng Soon, et al.
Publicado: (2019)

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

Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic
por: Pröbstel, Anne-Katrin, et al.
Publicado: (2016)

Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene
por: Brusa, Roberta, et al.
Publicado: (2020)

Enhancement of cranial nerves, conus medullaris, and nerve roots in POLG mitochondrial disease
por: Bayat, Michael, et al.
Publicado: (2019)

Tau Pathology Associated With Parkinsonism and Mutation of Mitochondrial DNA Helicase Gene TWNK
por: Vandenberghe, Wim, et al.
Publicado: (2021)

Pediatric anti-Hu–associated encephalitis with clinical features of Rasmussen encephalitis
por: Aravamuthan, Bhooma R., et al.
Publicado: (2015)

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity
por: Ladds, Emma, et al.
Publicado: (2018)

Novel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia
por: Bris, Celine, et al.
Publicado: (2017)

Forecasting stroke-like episodes and outcomes in mitochondrial disease
por: Ng, Yi Shiau, et al.
Publicado: (2021)

Cognitive deficits in adult m.3243A>G‐ and m.8344A>G‐related mitochondrial disease: importance of correcting for baseline intellectual ability
por: Moore, Heather L., et al.
Publicado: (2019)

Degos disease mimicking primary vasculitis of the CNS
por: Gmuca, Sabrina, et al.
Publicado: (2016)

Pembrolizumab for progressive multifocal leukoencephalopathy due to primary immunodeficiency
por: Küpper, Clemens, et al.
Publicado: (2019)

The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy
por: Vincent, Amy E., et al.
Publicado: (2016)

Microangiopathy in primary familial brain calcification: Evidence from skin biopsies
por: Nicolas, Gaël, et al.
Publicado: (2017)

Encephalomyeloneuropathy with CRMP-5 antibodies in a patient with a primary mediastinal serinoma
por: Hampton, Cliff W., et al.
Publicado: (2015)

Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB
por: Keogh, Michael J., et al.
Publicado: (2015)

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics
por: Pitceathly, Robert D. S., et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_99gsuh9kvq3thsvdk9ejp9rfj9