Cargando…
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene
Autores principales: | Brusa, Roberta, Mauri, Eleonora, Dell’Arti, Laura, Magri, Francesca, Ronchi, Dario, Minorini, Valeria, Mainetti, Claudia, Gagliardi, Delia, Faravelli, Irene, Meneri, Megi, Bresolin, Nereo, Viola, Francesco, Corti, Stefania, Comi, Giacomo Pietro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524578/ https://www.ncbi.nlm.nih.gov/pubmed/33062892 http://dx.doi.org/10.1212/NXG.0000000000000511 |
Ejemplares similares
-
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation
por: Scarcella, Simone, et al.
Publicado: (2023) -
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature
por: Costamagna, Gianluca, et al.
Publicado: (2020) -
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature
por: Gagliardi, Delia, et al.
Publicado: (2019) -
Diagnostic and Prognostic Role of Blood and Cerebrospinal Fluid and Blood Neurofilaments in Amyotrophic Lateral Sclerosis: A Review of the Literature
por: Gagliardi, Delia, et al.
Publicado: (2019) -
Subclinical Leber’s hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye
por: Mauri, Eleonora, et al.
Publicado: (2018)