Author:
Ogawa Masafumi,Shigeto Hiroshi,Yamamoto Toshiyuki,Oya Yasushi,Wada Keiji,Nishikawa Toru,Kawai Mitsuru
Subject
Neurology (clinical),Neurology
Reference23 articles.
1. Ataxia and hereditary disorders;Paulson;Neurol. Clin.,2001
2. TRH therapy of ataxia in patients with SCD;Sobue,1986
3. Glutamate dehydrogenase deficiency in three patients with spinocerebellar ataxia: a new enzymatic defect?;Plaitakis;Trans. Am. Neurol. Assoc.,1979
4. Glutamate dehydrogenase deficiency in spinocerebellar degenerations;Yamaguchi;Neurochem. Res.,1982
5. Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy;Kish;Ann. Neurol.,1991
Cited by
32 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