Saito M - Search Results

1

A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths.

Nakagawa M, Suehara M, Saito A, Takashima H, Umehara F, Saito M, Kanzato N, Matsuzaki T, Takenaga S, Sakoda S, Izumo S, Osame M. Nakagawa M, et al. Among authors: saito m, saito a. Neurology. 1999 Apr 12;52(6):1271-5. doi: 10.1212/wnl.52.6.1271. Neurology. 1999. PMID: 10214757

2

Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1.

Takashima H, Nakagawa M, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Terwilliger JD, Osame M. Takashima H, et al. Among authors: saito m, saito a. Neuromuscul Disord. 1999 Oct;9(6-7):368-71. doi: 10.1016/s0960-8966(99)00021-8. Neuromuscul Disord. 1999. PMID: 10545038

3

Hereditary motor and sensory neuropathy with proximal dominant involvement: clinical, pathological, and genetic features.

Nakagawa M, Takashima H, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Izumo S, Terwilliger JD, Osame M. Nakagawa M, et al. Among authors: saito m, saito a. Ann N Y Acad Sci. 1999 Sep 14;883:449-52. Ann N Y Acad Sci. 1999. PMID: 10586270 No abstract available.

4

Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease.

Takashima H, Nakagawa M, Umehara F, Hirata K, Suehara M, Mayumi H, Yoshishige K, Matsuyama W, Saito M, Jonosono M, Arimura K, Osame M. Takashima H, et al. Among authors: saito m. Acta Neurol Scand. 2003 Jan;107(1):31-7. doi: 10.1034/j.1600-0404.2003.01317.x. Acta Neurol Scand. 2003. PMID: 12542510

5

A C77G point mutation in CD45 exon 4, which is associated with the development of multiple sclerosis and increased susceptibility to HIV-1 infection, is undetectable in Japanese population.

Sabouri AH, Saito M, Matsumoto W, Kodama D, Farid R, Izumo S, Usuku K, Osame M. Sabouri AH, et al. Among authors: saito m. Eur J Neurol. 2003 Nov;10(6):737-9. doi: 10.1046/j.1468-1331.2003.00679.x. Eur J Neurol. 2003. PMID: 14641523

6

Chronic progressive cervical myelopathy with HTLV-I infection: Variant form of HAM/TSP?

Umehara F, Nagatomo S, Yoshishige K, Saito M, Furukawa Y, Usuku K, Osame M. Umehara F, et al. Among authors: saito m. Neurology. 2004 Oct 12;63(7):1276-80. doi: 10.1212/01.wnl.0000140496.03342.bc. Neurology. 2004. PMID: 15477551

7

Increased levels of soluble Fas ligand in CSF of rapidly progressive HTLV-1-associated myelopathy/tropical spastic paraparesis patients.

Saito M, Nakamura N, Nagai M, Shirakawa K, Sato H, Kawahigashi N, Furukawa Y, Usuku K, Nakagawa M, Izumo S, Osame M. Saito M, et al. J Neuroimmunol. 1999 Aug 3;98(2):221-6. doi: 10.1016/s0165-5728(99)00095-8. J Neuroimmunol. 1999. PMID: 10430056

8

An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy.

Saito A, Higuchi I, Nakagawa M, Saito M, Uchida Y, Inose M, Kasai T, Niiyama T, Fukunaga H, Arimura K, Osame M. Saito A, et al. Among authors: saito m. Muscle Nerve. 2000 Apr;23(4):490-7. doi: 10.1002/(sici)1097-4598(200004)23:4<490::aid-mus6>3.0.co;2-k. Muscle Nerve. 2000. PMID: 10716758

9

[A case of tabes dorsalis observed in an HTLV-1 carrier].

Nagata A, Saito M, Kanzato N, Matsuzaki T, Suehara M. Nagata A, et al. Among authors: saito m. Rinsho Shinkeigaku. 1997 Apr;37(4):341-3. Rinsho Shinkeigaku. 1997. PMID: 9248347 Japanese.

10

Localized scleroderma associated with progressing ischemic stroke.

Kanzato N, Matsuzaki T, Komine Y, Saito M, Saito A, Yoshio T, Suehara M. Kanzato N, et al. Among authors: saito m, saito a. J Neurol Sci. 1999 Feb 1;163(1):86-9. doi: 10.1016/s0022-510x(98)00267-6. J Neurol Sci. 1999. PMID: 10223417

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