Cargando…
Tracking a Fast-Moving Disease: Longitudinal Markers, Monitoring, and Clinical Trial Endpoints in ALS
Amyotrophic lateral sclerosis (ALS) encompasses a heterogeneous group of phenotypes with different progression rates, varying degree of extra-motor involvement and divergent progression patterns. The natural history of ALS is increasingly evaluated by large, multi-time point longitudinal studies, ma...
Autores principales: | Chipika, Rangariroyashe Hannah, Finegan, Eoin, Li Hi Shing, Stacey, Hardiman, Orla, Bede, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433752/ https://www.ncbi.nlm.nih.gov/pubmed/30941088 http://dx.doi.org/10.3389/fneur.2019.00229 |
Ejemplares similares
-
Pathological Crying and Laughing in Motor Neuron Disease: Pathobiology, Screening, Intervention
por: Finegan, Eoin, et al.
Publicado: (2019) -
Post-polio Syndrome: More Than Just a Lower Motor Neuron Disease
por: Li Hi Shing, Stacey, et al.
Publicado: (2019) -
Imaging data reveal divergent longitudinal trajectories in PLS, ALS and poliomyelitis survivors: Group-level and single-subject traits
por: Tahedl, Marlene, et al.
Publicado: (2021) -
Occulomotor Neural Integrator Dysfunction in Multiple Sclerosis: Insights From Neuroimaging
por: Bede, Peter, et al.
Publicado: (2018) -
Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology
por: Li Hi Shing, Stacey, et al.
Publicado: (2021)