Cargando…
Plasma LDH: A specific biomarker for lung affectation in COVID-19?
OBJECTIVES: We aimed to determine whether the plasma profile of lactate dehydrogenase (LDH) isoenzymes is altered in patients with COVID-19, and whether this is attributable to a specific release of LDH-3, the main LDH isoenzyme expressed in lungs. DESIGN: We collected fresh plasma aliquots from 17...
Autores principales: | Serrano-Lorenzo, Pablo, Coya, Olga N., López-Jimenez, Ana, Blázquez, Alberto, Delmiro, Aitor, Lucia, Alejandro, Arenas, Joaquín, Martín, Miguel A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058053/ https://www.ncbi.nlm.nih.gov/pubmed/33898686 http://dx.doi.org/10.1016/j.plabm.2021.e00226 |
Ejemplares similares
-
Pathophysiology of Cerebellar Degeneration in Mitochondrial Disorders: Insights from the Harlequin Mouse
por: Fernández de la Torre, Miguel, et al.
Publicado: (2023) -
Apoptosis-Inducing Factor Deficiency Induces Tissue-Specific Alterations in Autophagy: Insights from a Preclinical Model of Mitochondrial Disease and Exercise Training Effects
por: Laine-Menéndez, Sara, et al.
Publicado: (2022) -
Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report
por: González-Quintana, Adrián, et al.
Publicado: (2020) -
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population
por: Garcia-Solaesa, Virginia, et al.
Publicado: (2019) -
A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome
por: Rivera, Henry, et al.
Publicado: (2013)