Hayashi YK - Search Results

1

Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients.

Takeuchi F, Yonemoto N, Nakamura H, Shimizu R, Komaki H, Mori-Yoshimura M, Hayashi YK, Nishino I, Kawai M, Kimura E, Takeda S. Takeuchi F, et al. Among authors: hayashi yk. J Neurol. 2013 Dec;260(12):3023-9. doi: 10.1007/s00415-013-7104-y. Epub 2013 Sep 22. J Neurol. 2013. PMID: 24057148 Free PMC article.

2

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.

Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Hayashi YK, et al. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

3

Congenital muscular dystrophies.

Arahata K, Ishii H, Hayashi YK. Arahata K, et al. Among authors: hayashi yk. Curr Opin Neurol. 1995 Oct;8(5):385-90. doi: 10.1097/00019052-199510000-00011. Curr Opin Neurol. 1995. PMID: 8542045 Review.

4

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K. Hayashi YK, et al. Neurology. 2001 Jul 10;57(1):115-21. doi: 10.1212/wnl.57.1.115. Neurology. 2001. PMID: 11445638

5

Tongue atrophy in facioscapulohumeral muscular dystrophy.

Yamanaka G, Goto K, Matsumura T, Funakoshi M, Komori T, Hayashi YK, Arahata K. Yamanaka G, et al. Among authors: hayashi yk. Neurology. 2001 Aug 28;57(4):733-5. doi: 10.1212/wnl.57.4.733. Neurology. 2001. PMID: 11524495

6

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.

Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y. Tateyama M, et al. Among authors: hayashi yk. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2.323. Neurology. 2002. PMID: 11805270

7

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].

Yamanaka G, Goto K, Hayashi YK, Miyajima T, Hoshika A, Arahata K. Yamanaka G, et al. Among authors: hayashi yk. No To Hattatsu. 2002 Jul;34(4):318-24. No To Hattatsu. 2002. PMID: 12134683 Japanese.

8

[Recent advances in limb-girdle muscular dystrophy research].

Nonaka I, Minami N, Chae J, Hayashi YK, Nishino I, Arahata K. Nonaka I, et al. Among authors: hayashi yk. Rinsho Shinkeigaku. 2001 Dec;41(12):1194-7. Rinsho Shinkeigaku. 2001. PMID: 12235836 Review. Japanese.

9

[The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].

Onishi Y, Higuchi J, Ogawa T, Namekawa A, Hayashi H, Odakura H, Goto K, Hayashi YK. Onishi Y, et al. Among authors: hayashi h, hayashi yk. Rinsho Shinkeigaku. 2002 Feb;42(2):140-4. Rinsho Shinkeigaku. 2002. PMID: 12424964 Japanese.

10

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.

Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshima S, Kudoh J, Hentati F, Nishino I. Driss A, et al. Among authors: hayashi yk. Neurology. 2003 Apr 22;60(8):1341-4. doi: 10.1212/01.wnl.0000065886.82930.c5. Neurology. 2003. PMID: 12707439

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