Cargando…
Mitochondrial disease heterogeneity: a prognostic challenge
Mitochondrial diseases are a heterogeneous group of progressive, genetically transmitted, multisystem disorders caused by impaired mitochondrial function. The disease course for individuals with mitochondrial myopathies varies greatly from patient to patient because disease progression largely depen...
Autores principales: | Moggio, Maurizio, Colombo, Irene, Peverelli, Lorenzo, Villa, Luisa, Xhani, Rubjona, Testolin, Silvia, Di Mauro, Salvatore, Sciacco, Monica |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pacini Editore SpA
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299169/ https://www.ncbi.nlm.nih.gov/pubmed/25709378 |
Ejemplares similares
-
A case report with the peculiar concomitance of 2 different genetic syndromes
por: Lerario, Alberto, et al.
Publicado: (2016) -
Immune-mediated necrotizing myopathy due to statins exposure
por: VILLA, LUISA, et al.
Publicado: (2018) -
Nutritional Challenges in Duchenne Muscular Dystrophy
por: Salera, Simona, et al.
Publicado: (2017) -
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis
por: Magri, Francesca, et al.
Publicado: (2020) -
Coexistence of VHL Disease and CPT2 Deficiency: A Case Report
por: Ferrara, Alfonso Massimiliano, et al.
Publicado: (2016)