Goto Y - Search Results

1

Importance of CAG repeat length in childhood-onset dentatorubral-pallidoluysian atrophy.

Maruyama S, Saito Y, Nakagawa E, Saito T, Komaki H, Sugai K, Sasaki M, Kumada S, Saito Y, Tanaka H, Minami N, Goto Y. Maruyama S, et al. Among authors: goto y. J Neurol. 2012 Nov;259(11):2329-34. doi: 10.1007/s00415-012-6493-7. Epub 2012 Apr 18. J Neurol. 2012. PMID: 22527233

2

Early onset distal muscular dystrophy.

Kinoshita H, Sugai K, Goto Y, Nonaka I. Kinoshita H, et al. Among authors: goto y. Brain Dev. 1995 May-Jun;17(3):206-9. doi: 10.1016/0387-7604(95)00027-9. Brain Dev. 1995. PMID: 7573762 Review.

3

Progressive brainstem and white matter lesions in Kearns-Sayre syndrome: a case report.

Nakagawa E, Hirano S, Yamanouchi H, Goto Y, Nonaka I, Takashima S. Nakagawa E, et al. Among authors: goto y. Brain Dev. 1994 Sep-Oct;16(5):416-8. doi: 10.1016/0387-7604(94)90133-3. Brain Dev. 1994. PMID: 7892965

4

Severe central nervous system involvement in a patient with congenital fiber-type disproportion myopathy.

Nakagawa E, Ozawa M, Yamanouchi H, Sugai K, Goto Y, Nonaka I. Nakagawa E, et al. Among authors: goto y. J Child Neurol. 1996 Jan;11(1):71-3. doi: 10.1177/088307389601100119. J Child Neurol. 1996. PMID: 8745394 No abstract available.

5

Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome.

Nakagawa E, Osari S, Yamanouchi H, Matsuda H, Goto Y, Nonaka I. Nakagawa E, et al. Among authors: goto y. Brain Dev. 1996 Jan-Feb;18(1):68-70. doi: 10.1016/0387-7604(95)00096-8. Brain Dev. 1996. PMID: 8907347 Clinical Trial.

6

Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis.

Ikezawa M, Minami N, Takahashi M, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: goto y. Brain Dev. 1998 Apr;20(3):165-8. doi: 10.1016/s0387-7604(98)00012-6. Brain Dev. 1998. PMID: 9628192

7

MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathy.

Nishino I, Minami N, Kobayashi O, Ikezawa M, Goto Y, Arahata K, Nonaka I. Nishino I, et al. Among authors: goto y. Neuromuscul Disord. 1998 Oct;8(7):453-8. doi: 10.1016/s0960-8966(98)00075-3. Neuromuscul Disord. 1998. PMID: 9829274 Free article.

8

Differences in evoked potential characteristics between DRPLA patients and patients with progressive myoclonic epilepsy: preliminary findings indicating usefulness for differential diagnosis.

Kasai K, Onuma T, Kato M, Kato T, Takeya J, Sekimoto M, Watanabe K, Minami N, Goto Y, Minabe Y. Kasai K, et al. Among authors: goto y. Epilepsy Res. 1999 Oct;37(1):3-11. doi: 10.1016/s0920-1211(99)00028-5. Epilepsy Res. 1999. PMID: 10515170

9

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

Minami N, Nishino I, Kobayashi O, Ikezoe K, Goto Y, Nonaka I. Minami N, et al. Among authors: goto y. J Neurol Sci. 1999 Dec 1;171(1):31-7. doi: 10.1016/s0022-510x(99)00245-2. J Neurol Sci. 1999. PMID: 10567047

10

Rapid immunologic diagnosis of classic late infantile neuronal ceroid lipofuscinosis.

Kurachi Y, Oka A, Mizuguchi M, Ohkoshi Y, Sasaki M, Itoh M, Hayashi M, Goto Y, Takashima S. Kurachi Y, et al. Among authors: goto y. Neurology. 2000 Apr 25;54(8):1676-80. doi: 10.1212/wnl.54.8.1676. Neurology. 2000. PMID: 10762513

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