Hayasaka K - Search Results

1

[Abnormality of PMP-22 gene in Japanese patients with Charcot-Marie-Tooth disease--comparison between Southern blot and polymerase chain reaction analysis in the detection of PMP-22 gene duplication].

Yamamoto M, Sobue G, Kumazawa K, Doyu M, Mitsuma T, Hayasaka K. Yamamoto M, et al. Among authors: hayasaka k. No To Shinkei. 1995 Jul;47(7):687-91. No To Shinkei. 1995. PMID: 7612387 Japanese.

2

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Hattori N, et al. Among authors: hayasaka k. Brain. 2003 Jan;126(Pt 1):134-51. doi: 10.1093/brain/awg012. Brain. 2003. PMID: 12477701 Review.

3

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP.

Yamamoto M, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, Yanagihara T, Ikegami T, Yamamoto T, Ohashi H, Nishimura T, Mitsuma T, Kiyosawa H, Chance PF, Sobue G. Yamamoto M, et al. Among authors: hayasaka k. Hum Genet. 1997 Feb;99(2):151-4. doi: 10.1007/s004390050330. Hum Genet. 1997. PMID: 9048912

4

Facilitated diagnosis of CMT1A duplication in chromosome 17p11.2-12: analysis with a CMT1A-REP repeat probe and photostimulated luminescence imaging.

Ikegami T, Ikeda H, Chance PF, Kiyosawa H, Yamamoto M, Sobue G, Ohnishi A, Tachi N, Hayasaka K. Ikegami T, et al. Among authors: hayasaka k. Hum Mutat. 1997;9(6):563-6. doi: 10.1002/(SICI)1098-1004(1997)9:6<563::AID-HUMU10>3.0.CO;2-0. Hum Mutat. 1997. PMID: 9195231

5

Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeat.

Yamamoto M, Keller MP, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, Yanagihara T, Mitsuma T, Chance PF, Sobue G. Yamamoto M, et al. Among authors: hayasaka k. Hum Mutat. 1998;11(2):109-13. doi: 10.1002/(SICI)1098-1004(1998)11:2<109::AID-HUMU2>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9482573

6

[A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12].

Inoue M, Kojima M, Aikoh H, Sugai K, Murakami N, Nonaka I, Hayasaka K, Yamamoto M, Sobue G. Inoue M, et al. Among authors: hayasaka k. No To Hattatsu. 1999 Sep;31(5):452-7. No To Hattatsu. 1999. PMID: 10487071 Japanese.

7

Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation.

Kurihara S, Adachi Y, Imai C, Araki H, Hattori N, Numakura C, Lin Y, Hayasaka K, Sobue G, Nakashima K. Kurihara S, et al. Among authors: hayasaka k. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1492-4. doi: 10.1136/jnnp.2003.020107. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377707 Free PMC article.

8

Age associated axonal features in HNPP with 17p11.2 deletion in Japan.

Koike H, Hirayama M, Yamamoto M, Ito H, Hattori N, Umehara F, Arimura K, Ikeda S, Ando Y, Nakazato M, Kaji R, Hayasaka K, Nakagawa M, Sakoda S, Matsumura K, Onodera O, Baba M, Yasuda H, Saito T, Kira J, Nakashima K, Oka N, Sobue G. Koike H, et al. Among authors: hayasaka k. J Neurol Neurosurg Psychiatry. 2005 Aug;76(8):1109-14. doi: 10.1136/jnnp.2004.048140. J Neurol Neurosurg Psychiatry. 2005. PMID: 16024889 Free PMC article.

9

Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations.

Numakura C, Lin C, Ikegami T, Guldberg P, Hayasaka K. Numakura C, et al. Among authors: hayasaka k. Hum Mutat. 2002 Nov;20(5):392-8. doi: 10.1002/humu.10134. Hum Mutat. 2002. PMID: 12402337

10

Screening of the early growth response 2 gene in Japanese patients with Charcot-Marie-Tooth disease type 1.

Numakura C, Shirahata E, Yamashita S, Kanai M, Kijima K, Matsuki T, Hayasaka K. Numakura C, et al. Among authors: hayasaka k. J Neurol Sci. 2003 Jun 15;210(1-2):61-4. doi: 10.1016/s0022-510x(03)00028-5. J Neurol Sci. 2003. PMID: 12736090

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