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
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report.
Sprovieri T et al.
Bmc Medical Genetics, 2019
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