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Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.
Kuroha Y, Ishiguro T, Tada M, Hara N, Murayama K, Kawachi I, Kasuga K, Miyashita A, Hasegawa A, Takahashi T, Matsubara N, Onodera O, Kakita A, Koike R, Ikeuchi T. Kuroha Y, et al. Among authors: kawachi i. Neurol Genet. 2022 Sep 27;8(5):e200030. doi: 10.1212/NXG.0000000000200030. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36176336 Free PMC article.
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.
Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S. Date H, et al. Among authors: kawachi i. Nat Genet. 2001 Oct;29(2):184-8. doi: 10.1038/ng1001-184. Nat Genet. 2001. PMID: 11586299
[Gene diagnosis of patients with chorea].
Shimohata T, Onodera O, Honma Y, Hirota K, Nunomura Y, Kimura T, Kawachi I, Sanpei K, Nishizawa M, Tsuji S. Shimohata T, et al. Among authors: kawachi i. Rinsho Shinkeigaku. 2004 Mar;44(3):149-53. Rinsho Shinkeigaku. 2004. PMID: 15233265 Japanese.
Pathologic and immunologic profiles of a limited form of neuromyelitis optica with myelitis.
Yanagawa K, Kawachi I, Toyoshima Y, Yokoseki A, Arakawa M, Hasegawa A, Ito T, Kojima N, Koike R, Tanaka K, Kosaka T, Tan CF, Kakita A, Okamoto K, Tsujita M, Sakimura K, Takahashi H, Nishizawa M. Yanagawa K, et al. Among authors: kawachi i. Neurology. 2009 Nov 17;73(20):1628-37. doi: 10.1212/WNL.0b013e3181c1deb9. Neurology. 2009. PMID: 19917985
Cognitive impairment and cortical degeneration in neuromyelitis optica.
Saji E, Arakawa M, Yanagawa K, Toyoshima Y, Yokoseki A, Okamoto K, Otsuki M, Akazawa K, Kakita A, Takahashi H, Nishizawa M, Kawachi I. Saji E, et al. Among authors: kawachi i. Ann Neurol. 2013 Jan;73(1):65-76. doi: 10.1002/ana.23721. Ann Neurol. 2013. PMID: 23378324
1,293 results