Goto K - Search Results

1

Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation.

Mori-Yoshimura M, Mitsuhashi S, Nakamura H, Komaki H, Goto K, Yonemoto N, Takeuchi F, Hayashi YK, Murata M, Takahashi Y, Nishino I, Takeda S, Kimura E. Mori-Yoshimura M, et al. Among authors: goto k. J Neuromuscul Dis. 2018;5(2):193-203. doi: 10.3233/JND-170225. J Neuromuscul Dis. 2018. PMID: 29614690 Free PMC article.

2

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.

Goto K, Nishino I, Hayashi YK. Goto K, et al. 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

3

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

Nakamura H, Kimura E, Mori-Yoshimura M, Komaki H, Matsuda Y, Goto K, Hayashi YK, Nishino I, Takeda S, Kawai M. Nakamura H, et al. Among authors: goto k. Orphanet J Rare Dis. 2013 Apr 19;8:60. doi: 10.1186/1750-1172-8-60. Orphanet J Rare Dis. 2013. PMID: 23601510 Free PMC article.

4

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Okubo M, Minami N, Goto K, Goto Y, Noguchi S, Mitsuhashi S, Nishino I. Okubo M, et al. Among authors: goto y, goto k. J Hum Genet. 2016 Jun;61(6):483-9. doi: 10.1038/jhg.2016.7. Epub 2016 Feb 25. J Hum Genet. 2016. PMID: 26911353 Free PMC article.

5

Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations.

Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I. Hamanaka K, et al. Among authors: goto k. Neuromuscul Disord. 2016 Apr-May;26(4-5):300-8. doi: 10.1016/j.nmd.2016.03.001. Epub 2016 Mar 15. Neuromuscul Disord. 2016. PMID: 27061275

6

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.

Okubo M, Goto K, Komaki H, Nakamura H, Mori-Yoshimura M, Hayashi YK, Mitsuhashi S, Noguchi S, Kimura E, Nishino I. Okubo M, et al. Among authors: goto k. Orphanet J Rare Dis. 2017 Aug 31;12(1):149. doi: 10.1186/s13023-017-0703-4. Orphanet J Rare Dis. 2017. PMID: 28859693 Free PMC article.

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: goto k. No To Hattatsu. 2002 Jul;34(4):318-24. No To Hattatsu. 2002. PMID: 12134683 Japanese.

8

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: goto k. 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

9

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: goto k. 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

10

Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1).

Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I. Shalaby S, et al. Among authors: goto k. Neuromuscul Disord. 2008 Dec;18(12):959-61. doi: 10.1016/j.nmd.2008.09.012. Epub 2008 Oct 25. Neuromuscul Disord. 2008. PMID: 18952429

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