Cargando…
Skeletal muscle and motor deficits in Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is a genetic neurocutaneous disorder with multisystem manifestations, including a predisposition to tumor formation and bone dysplasias. Studies over the last decade have shown that NF1 can also be associated with significant motor deficits, such as poor coordination,...
Autores principales: | Summers, M.A., Quinlan, K.G., Payne, J.M., Little, D.G., North, K.N., Schindeler, A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Society of Musculoskeletal and Neuronal Interactions
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133719/ https://www.ncbi.nlm.nih.gov/pubmed/26032208 |
Ejemplares similares
-
COVID-19 signalome: Potential therapeutic interventions
por: Lundstrom, Kenneth, et al.
Publicado: (2023) -
Evaluating modified diets and dietary supplement therapies for reducing muscle lipid accumulation and improving muscle function in neurofibromatosis type 1 (NF1)
por: Vasiljevski, Emily R., et al.
Publicado: (2020) -
L‐carnitine supplementation for muscle weakness and fatigue in children with neurofibromatosis type 1: A Phase 2a clinical trial
por: Vasiljevski, Emily R., et al.
Publicado: (2021) -
A randomized controlled trial of remote microphone listening devices to treat auditory deficits in children with neurofibromatosis type 1
por: Rance, Gary, et al.
Publicado: (2022) -
The skeletal muscle phenotype of children with Neurofibromatosis Type 1 – A clinical perspective
por: Chinoy, Amish, et al.
Publicado: (2022)