Cargando…
The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
OBJECTIVE: We performed a prospective, cross‐sectional cognitive assessment in subjects with Duchenne Muscular Dystrophy (DMD) and their biological mothers. METHODS: Thirty subjects with out‐of‐frame mutations in the dystrophin (DMD) gene, and 25 biological mothers were evaluated using the National...
Autores principales: | Thangarajh, Mathula, Kaat, Aaron J., Bibat, Genila, Mansour, Jennifer, Summerton, Katherine, Gioia, Anthony, Berger, Carly, Hardy, Kristina K., Wagner, Kathryn R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764624/ https://www.ncbi.nlm.nih.gov/pubmed/31472009 http://dx.doi.org/10.1002/acn3.50867 |
Ejemplares similares
-
The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
Publicado: (2019) -
Longitudinal Evaluation of Working Memory in Duchenne Muscular Dystrophy
por: Thangarajh, Mathula, et al.
Publicado: (2020) -
The Relationship Between Bone Mineral Density and Cardiovascular Function in Duchenne Muscular Dystrophy: A Retrospective Cohort Study
por: Kervin, Tara, et al.
Publicado: (2018) -
Longitudinal functional and imaging outcome measures in FKRP limb-girdle muscular dystrophy
por: Leung, Doris G., et al.
Publicado: (2020) -
Neurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DNHS).
por: Thangarajh, Mathula, et al.
Publicado: (2018)