Cargando…
Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clue
BACKGROUND: The genetic landscape of neurodevelopmental disorders is constantly expanding and children with early-onset neurological phenotypes increasingly receive a genetic diagnosis. Nonetheless, the awareness of the chronic course of these conditions, and consequently their recognition and manag...
Autores principales: | Indelicato, Elisabetta, Zech, Michael, Amprosi, Matthias, Boesch, Sylvia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848801/ https://www.ncbi.nlm.nih.gov/pubmed/35172867 http://dx.doi.org/10.1186/s13023-022-02218-8 |
Ejemplares similares
-
Familial writer’s cramp: a clinical clue for inherited coenzyme Q(10) deficiency
por: Amprosi, Matthias, et al.
Publicado: (2020) -
Instrumented gait analysis defines the walking signature of CACNA1A disorders
por: Indelicato, Elisabetta, et al.
Publicado: (2021) -
The electrophysiological footprint of CACNA1A disorders
por: Indelicato, Elisabetta, et al.
Publicado: (2021) -
Toward the Definition of Patient-Reported Outcome Measurements in Hereditary Spastic Paraplegia
por: Amprosi, Matthias, et al.
Publicado: (2023) -
Skeletal muscle proteome analysis underpins multifaceted mitochondrial dysfunction in Friedreich’s ataxia
por: Indelicato, Elisabetta, et al.
Publicado: (2023)