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[The genetics of corticobasal syndrome].
Doi H, Tanaka F. Doi H, et al. Among authors: tanaka f. Brain Nerve. 2013 Jan;65(1):19-30. Brain Nerve. 2013. PMID: 23300100 Review. Japanese.
A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy.
Higashiyama Y, Doi H, Wakabayashi M, Tsurusaki Y, Miyake N, Saitsu H, Ohba C, Fukai R, Miyatake S, Joki H, Koyano S, Suzuki Y, Tanaka F, Kuroiwa Y, Matsumoto N. Higashiyama Y, et al. Among authors: tanaka f. Mov Disord. 2013 Apr;28(4):552-3. doi: 10.1002/mds.25296. Epub 2013 Jan 16. Mov Disord. 2013. PMID: 23325613 No abstract available.
Ablation of keratan sulfate accelerates early phase pathogenesis of ALS.
Hirano K, Ohgomori T, Kobayashi K, Tanaka F, Matsumoto T, Natori T, Matsuyama Y, Uchimura K, Sakamoto K, Takeuchi H, Hirakawa A, Suzumura A, Sobue G, Ishiguro N, Imagama S, Kadomatsu K. Hirano K, et al. Among authors: tanaka f. PLoS One. 2013 Jun 25;8(6):e66969. doi: 10.1371/journal.pone.0066969. Print 2013. PLoS One. 2013. PMID: 23825599 Free PMC article.
Identification of a novel homozygous SPG7 mutation in a Japanese patient with spastic ataxia: making an efficient diagnosis using exome sequencing for autosomal recessive cerebellar ataxia and spastic paraplegia.
Doi H, Ohba C, Tsurusaki Y, Miyatake S, Miyake N, Saitsu H, Kawamoto Y, Yoshida T, Koyano S, Suzuki Y, Kuroiwa Y, Tanaka F, Matsumoto N. Doi H, et al. Among authors: tanaka f. Intern Med. 2013;52(14):1629-33. doi: 10.2169/internalmedicine.52.0252. Epub 2013 Jul 15. Intern Med. 2013. PMID: 23857099 Free article.
Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood.
Ohba C, Osaka H, Iai M, Yamashita S, Suzuki Y, Aida N, Shimozawa N, Takamura A, Doi H, Tomita-Katsumoto A, Nishiyama K, Tsurusaki Y, Nakashima M, Miyake N, Eto Y, Tanaka F, Matsumoto N, Saitsu H. Ohba C, et al. Among authors: tanaka f. Neurogenetics. 2013 Nov;14(3-4):225-32. doi: 10.1007/s10048-013-0375-8. Epub 2013 Oct 4. Neurogenetics. 2013. PMID: 24091540
[Genetic background of corticobasal syndrome].
Doi H, Tanaka F. Doi H, et al. Among authors: tanaka f. Rinsho Shinkeigaku. 2013;53(11):1026-8. doi: 10.5692/clinicalneurol.53.1026. Rinsho Shinkeigaku. 2013. PMID: 24291868 Review. Japanese.
1,722 results