Cargando…
Paroxysmal Dyskinesia in Children: from Genes to the Clinic
BACKGROUND AND PURPOSE: Paroxysmal dyskinesia is a genetically and clinically heterogeneous movement disorder. Recent studies have shown that it exhibits both phenotype and genotype overlap with other paroxysmal disorders as well as clinical heterogeneity. We investigated the clinical and genetic ch...
Autores principales: | Kim, Soo Yeon, Lee, Jin Sook, Kim, Woo Joong, Kim, Hyuna, Choi, Sun Ah, Lim, Byung Chan, Kim, Ki Joong, Chae, Jong-Hee |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172489/ https://www.ncbi.nlm.nih.gov/pubmed/30198221 http://dx.doi.org/10.3988/jcn.2018.14.4.492 |
Ejemplares similares
-
Clinical Experience with Perampanel in Intractable Focal Epilepsy Over 12 Months of Follow-Up
por: Kim, Soo Yeon, et al.
Publicado: (2018) -
Diagnostic Challenges Associated with GLUT1 Deficiency: Phenotypic Variabilities and Evolving Clinical Features
por: Kim, Hyuna, et al.
Publicado: (2019) -
Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability
por: Lee, Jin Sook, et al.
Publicado: (2018) -
Clinical and Genetic Spectrum of ATP1A3-Related Disorders in a Korean Pediatric Population
por: Kim, Woo Joong, et al.
Publicado: (2020) -
A Case of Multiple Mitochondrial Dysfunctions Syndrome 4 with Novel ISCA2 Variants, Mimicking Post-Infectious Encephalitis
por: Chin, Hyungjin, et al.
Publicado: (2023)