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Prospective 10-year surveillance of human prion diseases in Japan.
Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, Takeda M, Kuroda S, Abe K, Murai H, Murayama S, Tateishi J, Takumi I, Shirabe S, Harada M, Sadakane A, Yamada M. Nozaki I, et al. Among authors: abe k. Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20. Brain. 2010. PMID: 20855418
Demyelinating peripheral neuropathy in Devic disease.
Aimoto Y, Ito K, Moriwaka F, Tashiro K, Abe K. Aimoto Y, et al. Among authors: abe k. Jpn J Psychiatry Neurol. 1991 Dec;45(4):861-4. doi: 10.1111/j.1440-1819.1991.tb00525.x. Jpn J Psychiatry Neurol. 1991. PMID: 1667535
[A family of paramyotonia congenita].
Houzen H, Maruo Y, Moriwaka F, Tashiro K, Abe K. Houzen H, et al. Among authors: abe k. Rinsho Shinkeigaku. 1993 Apr;33(4):452-4. Rinsho Shinkeigaku. 1993. PMID: 8396519 Review. Japanese.
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
Takahashi Y, Fukuda Y, Yoshimura J, Toyoda A, Kurppa K, Moritoyo H, Belzil VV, Dion PA, Higasa K, Doi K, Ishiura H, Mitsui J, Date H, Ahsan B, Matsukawa T, Ichikawa Y, Moritoyo T, Ikoma M, Hashimoto T, Kimura F, Murayama S, Onodera O, Nishizawa M, Yoshida M, Atsuta N, Sobue G; JaCALS; Fifita JA, Williams KL, Blair IP, Nicholson GA, Gonzalez-Perez P, Brown RH Jr, Nomoto M, Elenius K, Rouleau GA, Fujiyama A, Morishita S, Goto J, Tsuji S. Takahashi Y, et al. Am J Hum Genet. 2013 Nov 7;93(5):900-5. doi: 10.1016/j.ajhg.2013.09.008. Epub 2013 Oct 10. Am J Hum Genet. 2013. PMID: 24119685 Free PMC article.
7,014 results