Associated Papers
Neonatal Hyperekplexia: Is It Still a Diagnostic Challenge? Evidence From a Systematic Review.
Falsaperla R et al.
Journal of Child Neurology, 2024
Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.
Zhan F et al.
Journal of Clinical Neurology (seoul, Korea), 2020
Familial Hyperekplexia, a Potential Cause of Cautious Gait: A New Korean Case and a Systematic Review of Phenotypes
Lee Y et al.
Journal of Movement Disorders, 2017
Clinical features and genetic analysis of children with hyperekplexia in Korea.
Lee CG et al.
Journal of Child Neurology, 2013
Clinical and genetic analysis of three Korean children with pyridoxine-dependent epilepsy.
Nam SH et al.
Annals of Clinical and Laboratory Science, 2012
Identification of a de novo Lys304Gln mutation in the glycine receptor alpha-1 subunit gene in a Korean infant with hyperekplexia.
Kang HC et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2008
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