Startle disease—hyperekplexia (two sibling cases)
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology,General Medicine
Reference16 articles.
1. Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q;Ryan;American Journal of Human Genetics,1992
2. Startle disease or hyperekplexia further deliniation of the syndrome;Andermann;Brain,1980
3. Audiogenic startle reflex of man and its relationship to startle syndromes;Wilkins;Brain,1986
4. Hyperekplexia. A hereditary startle syndrome;Suhren;Journal of Neurosurgical Science,1966
5. Low cerebrospinal fluid concentration of free gamma-aminobutyric acid in startle disease;Dubowits;Lancet,1992
Cited by 4 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: Treatment of a Severe Phenotype and Review of the Literature;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2011-05
2. Congenital hyperekplexia: five sporadic cases;European Journal of Pediatrics;2005-10-07
3. Sporadic major hyperekplexia in neonates and infants: clinical manifestations and outcome;Pediatric Neurology;2004-07
4. Genetic defects in ion channels and neurological diseases in clinical, genetic and physiological aspects;Neurology Bulletin;2000-05-15
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