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Study on surgical treatment of intractable childhood epilepsy.
Mukahira K, Oguni H, Awaya Y, Tanaka T, Saito K, Shimizu H, Oda M, Arai N, Suzuki I, Osawa M. Mukahira K, et al. Among authors: oda m. Brain Dev. 1998 Apr;20(3):154-64. doi: 10.1016/s0387-7604(98)00008-4. Brain Dev. 1998. PMID: 9628191
Surgical indication for refractory childhood epilepsy.
Oguni H, Mukahira K, Tanaka T, Awaya Y, Saito K, Shimizu H, Oda M, Arai N, Suzuki I, Osawa M. Oguni H, et al. Among authors: oda m. Epilepsia. 2000;41 Suppl 9:21-5. doi: 10.1111/j.1528-1157.2000.tb02214.x. Epilepsia. 2000. PMID: 11156505 Free article.
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.
[A case of porcelain gallbladder with reference to reported cases in Japan].
Itsuji S, Munakata Y, Ishii M, Funatsu K, Mizuno Y, Ishida M, Tanaka T, Katoh S, Gibo K, Oda M, et al. Itsuji S, et al. Among authors: oda m. Nihon Shokakibyo Gakkai Zasshi. 1986 Apr;83(4):849-54. Nihon Shokakibyo Gakkai Zasshi. 1986. PMID: 3735738 Japanese. No abstract available.
2,012 results