FAMILIAL CEREBELLAR ATAXIA AND HYPOGONADISM
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/87/3/463/902359/87-3-463.pdf
Cited by 43 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. Hypergonadotrophic Hypogonadism with Cerebellar Ataxia in a Twenty-Six-Year-Old Female: A Case Report;Open Journal of Modern Neurosurgery;2024
2. Boucher–Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literature;Journal of Neurology;2014-10-31
3. Other autosomal recessive and childhood ataxias;Handbook of Clinical Neurology;2012
4. Complex movement disorders in a sporadic Boucher-Neuhäuser Syndrome: Phenotypic manifestations beyond the triad;Movement Disorders;2009-11-15
5. Hypergonadotropic Hypogonadism in Oligophrenia;Acta Medica Scandinavica;2009-04-24
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