Yamanaka G - Search Results

1

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: yamanaka g. 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

2

Tongue atrophy in facioscapulohumeral muscular dystrophy.

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

3

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

4

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: yamanaka g. BMC Neurol. 2002 Aug 20;2:7. doi: 10.1186/1471-2377-2-7. BMC Neurol. 2002. PMID: 12188928 Free PMC article.

5

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. 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

6

Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrest.

Kawashima H, Ishii C, Yamanaka G, Ioi H, Nishimata S, Kashiwagi Y, Takekuma K, Miyajima T, Hoshika A, Nishino I, Nonaka I. Kawashima H, et al. Among authors: yamanaka g. Pediatr Int. 2011 Apr;53(2):159-61. doi: 10.1111/j.1442-200X.2010.03211.x. Pediatr Int. 2011. PMID: 21501304

7

Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathy.

Nishikawa A, Iida A, Hayashi S, Okubo M, Oya Y, Yamanaka G, Takahashi I, Nonaka I, Noguchi S, Nishino I. Nishikawa A, et al. Among authors: yamanaka g. Mol Genet Genomic Med. 2019 May;7(5):e621. doi: 10.1002/mgg3.621. Epub 2019 Mar 18. Mol Genet Genomic Med. 2019. PMID: 30884204 Free PMC article.

8

Beta-propeller protein-associated neurodegeneration presenting Rett-like features: A case report and literature review.

Kano K, Yamanaka G, Muramatsu K, Morichi S, Ishida Y, Takamatsu T, Suzuki S, Miyajima T, Nakagawa E, Nishino I, Kawashima H. Kano K, et al. Among authors: yamanaka g. Am J Med Genet A. 2021 Feb;185(2):579-583. doi: 10.1002/ajmg.a.61993. Epub 2020 Nov 30. Am J Med Genet A. 2021. PMID: 33251766

9

Diagnostic and predictive value of CSF d-ROM level in influenza virus-associated encephalopathy.

Yamanaka G, Kawashima H, Suganami Y, Watanabe C, Watanabe Y, Miyajima T, Takekuma K, Oguchi S, Hoshika A. Yamanaka G, et al. J Neurol Sci. 2006 Apr 15;243(1-2):71-5. doi: 10.1016/j.jns.2005.11.029. Epub 2006 Jan 18. J Neurol Sci. 2006. PMID: 16413581

10

Increased level of serum interleukin-1 receptor antagonist subsequent to resolution of clinical symptoms in patients with West syndrome.

Yamanaka G, Kawashima H, Oana S, Ishida Y, Miyajima T, Kashiwagi Y, Hoshika A. Yamanaka G, et al. J Neurol Sci. 2010 Nov 15;298(1-2):106-9. doi: 10.1016/j.jns.2010.07.018. J Neurol Sci. 2010. PMID: 20807663

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