Cargando…
Qualitative exploration of the lived experience of adults diagnosed with primary mitochondrial disease
Primary mitochondrial disease (PMD) encompasses a heterogeneous group of energy deficiency disorders that are typically progressive, with affected individuals experiencing an average of 16 multisystem symptoms. Clinical trials are emerging, but current treatment options remain limited. In PMD, the e...
Autores principales: | Valverde, Kathleen D., McCormick, Elizabeth M., Falk, Marni J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458611/ https://www.ncbi.nlm.nih.gov/pubmed/36101828 http://dx.doi.org/10.1002/jmd2.12316 |
Ejemplares similares
-
Desmin common mutation is associated with multi-systemic disease manifestations and depletion of mitochondria and mitochondrial DNA
por: McCormick, Elizabeth M., et al.
Publicado: (2015) -
Qualitative study exploring patients experiences of being diagnosed and living with primary bone cancer in the UK
por: Martins, Ana, et al.
Publicado: (2019) -
Mitochondrial disease patient motivations and barriers to participate in clinical trials
por: Zolkipli-Cunningham, Zarazuela, et al.
Publicado: (2018) -
Endocrine Disorders in Primary Mitochondrial Disease
por: Al-Gadi, Iman S, et al.
Publicado: (2018) -
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain Function
por: Li, Dong, et al.
Publicado: (2016)