Hayashi YK - Search Results

1

Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients.

Matsumura T, Goto K, Yamanaka G, Lee JH, Zhang C, Hayashi YK, Arahata K. Matsumura T, et al. Among authors: hayashi yk. BMC Neurol. 2002 Aug 20;2:7. doi: 10.1186/1471-2377-2-7. BMC Neurol. 2002. PMID: 12188928 Free PMC article.

2

[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.

3

FSHD-like patients without 4q35 deletion.

Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK. Yamanaka G, et al. Among authors: hayashi yk. J Neurol Sci. 2004 Apr 15;219(1-2):89-93. doi: 10.1016/j.jns.2003.12.010. J Neurol Sci. 2004. PMID: 15050443

4

[Recent advances in facioscapulohumeral muscular dystrophy].

Hayashi YK, Goto K, Nishio I. Hayashi YK, et al. Rinsho Shinkeigaku. 2012;52(11):1154-7. doi: 10.5692/clinicalneurol.52.1154. Rinsho Shinkeigaku. 2012. PMID: 23196547 Japanese.

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

Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.

Tagawa K, Ogawa M, Kawabe K, Yamanaka G, Matsumura T, Goto K, Nonaka I, Nishino I, Hayashi YK. Tagawa K, et al. Among authors: hayashi yk. J Neurol Sci. 2003 Jul 15;211(1-2):23-8. doi: 10.1016/s0022-510x(03)00041-8. J Neurol Sci. 2003. PMID: 12767493

7

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.

Goto K, Nishino I, Hayashi YK. Goto K, et al. Among authors: hayashi yk. Neuromuscul Disord. 2006 Apr;16(4):256-61. doi: 10.1016/j.nmd.2006.01.008. Epub 2006 Mar 20. Neuromuscul Disord. 2006. PMID: 16545566

8

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

9

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.

10

[The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].

Hayashi YK, Arahata K. Hayashi YK, et al. Nihon Rinsho. 1997 Dec;55(12):3165-8. Nihon Rinsho. 1997. PMID: 9436429 Review. Japanese.

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