Nagamitsu S - Search Results

1

A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.

Nagamitsu S, Matsuura T, Khajavi M, Armstrong R, Gooch C, Harati Y, Ashizawa T. Nagamitsu S, et al. Neurology. 2000 Dec 12;55(11):1697-703. doi: 10.1212/wnl.55.11.1697. Neurology. 2000. PMID: 11113225

2

Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

Tan EK, Matsuura T, Nagamitsu S, Khajavi M, Jankovic J, Ashizawa T. Tan EK, et al. Among authors: nagamitsu s. Neurology. 2000 Mar 14;54(5):1195-8. doi: 10.1212/wnl.54.5.1195. Neurology. 2000. PMID: 10720300

3

Myotonic dystrophies.

Nagamitsu S, Ashizawa T. Nagamitsu S, et al. Adv Neurol. 2002;88:293-314. Adv Neurol. 2002. PMID: 11908232 Review. No abstract available.

4

Variability and validity of polymorphism association studies in Parkinson's disease.

Tan EK, Khajavi M, Thornby JI, Nagamitsu S, Jankovic J, Ashizawa T. Tan EK, et al. Among authors: nagamitsu s. Neurology. 2000 Aug 22;55(4):533-8. doi: 10.1212/wnl.55.4.533. Neurology. 2000. PMID: 10953187

5

Alcohol dehydrogenase polymorphism and Parkinson's disease.

Tan EK, Nagamitsu S, Matsuura T, Khajavi M, Jankovic J, Ondo W, Ashizawa T. Tan EK, et al. Among authors: nagamitsu s. Neurosci Lett. 2001 Jun 1;305(1):70-2. doi: 10.1016/s0304-3940(01)01770-0. Neurosci Lett. 2001. PMID: 11356310

6

Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit.

Waragai M, Nagamitsu S, Xu W, Li YJ, Lin X, Ashizawa T. Waragai M, et al. Among authors: nagamitsu s. J Neurosci Res. 2006 May 15;83(7):1170-8. doi: 10.1002/jnr.20807. J Neurosci Res. 2006. PMID: 16498633

7

Decreased CSF levels of substance P in patients with congenital sensory neuropathy with anhidrosis.

Nagamitsu S, Matsuishi T, Ohnishi A, Kato H. Nagamitsu S, et al. Neurology. 1997 Apr;48(4):1133. doi: 10.1212/wnl.48.4.1133. Neurology. 1997. PMID: 9109918 No abstract available.

8

Decreased cerebrospinal fluid levels of beta-endorphin in Japanese patients with Joseph disease.

Matsuishi T, Sakai T, Nagamitsu S, Komori H, Iwashita H, Kato H. Matsuishi T, et al. Among authors: nagamitsu s. Ann Neurol. 1994 Sep;36(3):441-3. doi: 10.1002/ana.410360317. Ann Neurol. 1994. PMID: 8080253

9

Serial magnetic resonance images in a patient with congenital sensory neuropathy with anhidrosis and complications resembling heat stroke.

Iwanaga R, Matsuishi T, Ohnishi A, Nakashima M, Abe T, Ohtaki E, Kojima K, Nagamitsu S, Ohbu K, Kato H. Iwanaga R, et al. Among authors: nagamitsu s. J Neurol Sci. 1996 Oct;142(1-2):79-84. doi: 10.1016/0022-510x(96)00152-9. J Neurol Sci. 1996. PMID: 8902724

10

Decreased cerebrospinal fluid levels of substance P in Machado-Joseph disease.

Matsuishi T, Sakai T, Nagamitsu S, Shoji H, Ueda N, Kaneko S, Kano T, Iwashita H, Kato H. Matsuishi T, et al. Among authors: nagamitsu s. J Neurol Sci. 1996 Oct;142(1-2):107-10. doi: 10.1016/0022-510x(96)00159-1. J Neurol Sci. 1996. PMID: 8902728

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