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Is Parkinson's disease a mitochondrial disorder?
Nakagawa-Hattori Y, Yoshino H, Kondo T, Mizuno Y, Horai S. Nakagawa-Hattori Y, et al. Among authors: yoshino h. J Neurol Sci. 1992 Jan;107(1):29-33. doi: 10.1016/0022-510x(92)90205-y. J Neurol Sci. 1992. PMID: 1578231
Mitochondrial dysfunction in Parkinson's disease.
Mizuno Y, Yoshino H, Ikebe S, Hattori N, Kobayashi T, Shimoda-Matsubayashi S, Matsumine H, Kondo T. Mizuno Y, et al. Among authors: yoshino h. Ann Neurol. 1998 Sep;44(3 Suppl 1):S99-109. doi: 10.1002/ana.410440715. Ann Neurol. 1998. PMID: 9749580 Review.
Polymorphism in the parkin gene in sporadic Parkinson's disease.
Wang M, Hattori N, Matsumine H, Kobayashi T, Yoshino H, Morioka A, Kitada T, Asakawa S, Minoshima S, Shimizu N, Mizuno Y. Wang M, et al. Among authors: yoshino h. Ann Neurol. 1999 May;45(5):655-8. doi: 10.1002/1531-8249(199905)45:5<655::aid-ana15>3.0.co;2-g. Ann Neurol. 1999. PMID: 10319889
Progress in familial Parkinson's disease.
Mizuno Y, Hattori N, Yoshino H, Hatano Y, Satoh K, Tomiyama H, Li Y. Mizuno Y, et al. Among authors: yoshino h. J Neural Transm Suppl. 2006;(70):191-204. doi: 10.1007/978-3-211-45295-0_30. J Neural Transm Suppl. 2006. PMID: 17017529 Review.
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Hattori N, et al. Among authors: yoshino h. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438
1,061 results