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Triple A syndrome in Japan.
Ikeda M, Hirano M, Shinoda K, Katsumata N, Furutama D, Nakamura K, Ikeda S, Tanaka T, Hanafusa T, Kitajima H, Kohno H, Nakagawa M, Nakamura Y, Ueno S. Ikeda M, et al. Among authors: nakamura y, nakamura k. Muscle Nerve. 2013 Sep;48(3):381-6. doi: 10.1002/mus.23770. Epub 2013 Jul 17. Muscle Nerve. 2013. PMID: 23861206
Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.
Yoshida K, Shimizu Y, Morita H, Okano T, Sakai H, Ohata T, Matsumoto N, Nakamura K, Tazawa K, Ohara S, Tabata K, Inoue A, Sato S, Shimojima Y, Hattori T, Ushiyama M, Ikeda S. Yoshida K, et al. Among authors: nakamura k. Cerebellum. 2009 Mar;8(1):46-51. doi: 10.1007/s12311-008-0062-8. Cerebellum. 2009. PMID: 18855094
Cerebral hemorrhage in Fabry's disease.
Nakamura K, Sekijima Y, Nakamura K, Hattori K, Nagamatsu K, Shimizu Y, Yasude T, Ushiyama M, Endo F, Fukushima Y, Ikeda S. Nakamura K, et al. J Hum Genet. 2010 Apr;55(4):259-61. doi: 10.1038/jhg.2010.18. Epub 2010 Mar 19. J Hum Genet. 2010. PMID: 20300124
Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation.
Shimazaki H, Honda J, Naoi T, Namekawa M, Nakano I, Yazaki M, Nakamura K, Yoshida K, Ikeda S, Ishiura H, Fukuda Y, Takahashi Y, Goto J, Tsuji S, Takiyama Y. Shimazaki H, et al. Among authors: nakamura k. J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):1024-8. doi: 10.1136/jnnp-2013-306981. Epub 2014 Feb 12. J Neurol Neurosurg Psychiatry. 2014. PMID: 24521565
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