Kawata A - Search Results

1

[Clinical and myopathological studies on rigid spine syndrome].

Isozaki E, Fujimoto Y, Kawata A, Matsubara S, Hirai S. Isozaki E, et al. Among authors: kawata a. Rinsho Shinkeigaku. 1996 Oct;36(10):1136-42. Rinsho Shinkeigaku. 1996. PMID: 8997137 Japanese.

2

[A family of SCA1 with pigmentary macular dystrophy].

Kouno R, Kawata A, Yoshida H, Ikeda S, Suda M, Hirai S. Kouno R, et al. Among authors: kawata a. Rinsho Shinkeigaku. 1999 Jun;39(6):649-52. Rinsho Shinkeigaku. 1999. PMID: 10502991 Japanese.

3

Autonomic failure in ALS with a novel SOD1 gene mutation.

Shimizu T, Kawata A, Kato S, Hayashi M, Takamoto K, Hayashi H, Hirai S, Yamaguchi S, Komori T, Oda M. Shimizu T, et al. Among authors: kawata a. Neurology. 2000 Apr 11;54(7):1534-7. doi: 10.1212/wnl.54.7.1534. Neurology. 2000. PMID: 10751275

4

[Clinical features of autosomal dominant spinocerebellar ataxias genetically unclassified into any known triplet-repeat diseases].

Aoki K, Kawata A, Suda M, Hirai S. Aoki K, et al. Among authors: kawata a. Rinsho Shinkeigaku. 2001 Jan;41(1):18-23. Rinsho Shinkeigaku. 2001. PMID: 11433762 Japanese.

5

Experimental allergic myositis in SJL/J mouse. Reappraisal of immune reaction based on changes after single immunization.

Matsubara S, Kitaguchi T, Kawata A, Miyamoto K, Yagi H, Hirai S. Matsubara S, et al. Among authors: kawata a. J Neuroimmunol. 2001 Oct 1;119(2):223-30. doi: 10.1016/s0165-5728(01)00377-0. J Neuroimmunol. 2001. PMID: 11585625

6

Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene.

Kawata A, Kato S, Hayashi H, Hirai S. Kawata A, et al. J Neurol Sci. 1997 Dec 9;153(1):82-5. doi: 10.1016/s0022-510x(97)00176-7. J Neurol Sci. 1997. PMID: 9455983

7

Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvement.

Mochizuki Y, Isozaki E, Takao M, Hashimoto T, Shibuya M, Arai M, Hosokawa M, Kawata A, Oyanagi K, Mihara B, Mizutani T. Mochizuki Y, et al. Among authors: kawata a. J Neurol Sci. 2012 Dec 15;323(1-2):85-92. doi: 10.1016/j.jns.2012.08.016. Epub 2012 Sep 11. J Neurol Sci. 2012. PMID: 22980027

8

Aberrant splicing of human Cu/Zn superoxide dismutase (SOD1) RNA transcripts.

Kawata A, Kato S, Shimizu T, Hayashi H, Hirai S, Misawa H, Takahashi R. Kawata A, et al. Neuroreport. 2000 Aug 21;11(12):2649-53. doi: 10.1097/00001756-200008210-00009. Neuroreport. 2000. PMID: 10976937

9

Masseter inhibitory reflex in amyotrophic lateral sclerosis.

Shimizu T, Komori T, Kato S, Kawata A, Hayashi H, Hirai S. Shimizu T, et al. Among authors: kawata a. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Dec;2(4):189-95. doi: 10.1080/14660820152882197. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001. PMID: 11958730

10

Neuropathological features of Japanese familial amyotrophic lateral sclerosis with p.N352S mutation in TARDBP.

Homma T, Nagaoka U, Kawata A, Mochizuki Y, Kawakami H, Maruyama H, Matsubara S, Komori T. Homma T, et al. Among authors: kawata a. Neuropathol Appl Neurobiol. 2014 Feb;40(2):231-6. doi: 10.1111/nan.12090. Neuropathol Appl Neurobiol. 2014. PMID: 24117534 No abstract available.

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