Familiar Hyperekplexia, a Potential Cause of Cautious Gait: A New Korean Case and a Systematic Review of Phenotypes-Reference-Cited by-同舟云学术

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Familiar Hyperekplexia, a Potential Cause of Cautious Gait: A New Korean Case and a Systematic Review of Phenotypes

Published:2017-01-25 Issue:1 Volume:10 Page:53-58
ISSN:2005-940X
Container-title:Journal of Movement Disorders
language:en
Short-container-title:JMD

Author:

Lee Yoonju,Kim Nan Young,Hong Sangkyoon,Chung Su Jin,Jeong Seong Ho,Lee Phil Hyu,Sohn Young H.

Publisher

The Korean Movement Disorder Society

Subject

Clinical Neurology,Neurology

Link

http://e-jmd.org/upload/jmd-16044.pdf

Reference7 articles.

1. Hyperekplexia: a treatable neurogenetic disease

2. Startle syndromes

3. Hyperekplexia Associated With Apnea and Sudden Infant Death Syndrome

4. Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hyperekplexia: A Single-Center Experience;Journal of Child Neurology;2024-06

2. Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene;Parkinsonism & Related Disorders;2022-12

3. Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes;Pediatric Neurology;2022-07

4. Paroxysmal Nonepileptic Events in Children;Neurology: Clinical Practice;2022-04-21

5. Advances in hyperekplexia and other startle syndromes;Neurological Sciences;2021-08-11

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