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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: hattori n. Ann Neurol. 1998 Sep;44(3 Suppl 1):S99-109. doi: 10.1002/ana.410440715. Ann Neurol. 1998. PMID: 9749580 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. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438
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: hattori n. 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
Genetics of Parkinson's disease.
Mizuno Y, Hattori N, Mori H. Mizuno Y, et al. Among authors: hattori n. Biomed Pharmacother. 1999 Apr;53(3):109-16. doi: 10.1016/S0753-3322(99)80075-4. Biomed Pharmacother. 1999. PMID: 10349506 Review.
[The Parkin gene and its product in AR-JP].
Hattori N, Mizuno Y. Hattori N, et al. No To Shinkei. 1999 Jun;51(6):493-500. No To Shinkei. 1999. PMID: 10423751 Japanese. No abstract available.
2,555 results