Nakazato M - Search Results

1

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form.

Koike H, Misu K, Ikeda S, Ando Y, Nakazato M, Ando E, Yamamoto M, Hattori N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Koike H, et al. Among authors: nakazato m. Arch Neurol. 2002 Nov;59(11):1771-6. doi: 10.1001/archneur.59.11.1771. Arch Neurol. 2002. PMID: 12433265

2

Type I familial amyloidotic polyneuropathy in Japan.

Nakazato M, Shiomi K, Miyazato M, Matsukura S. Nakazato M, et al. Intern Med. 1992 Dec;31(12):1335-8. doi: 10.2169/internalmedicine.31.1335. Intern Med. 1992. PMID: 1300167 Free article.

3

Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy.

Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A. Yoshinaga T, et al. Among authors: nakazato m. Neurology. 1992 Oct;42(10):2045-7. doi: 10.1212/wnl.42.10.2045. Neurology. 1992. PMID: 1407590

4

Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy.

Ikeda S, Nakano T, Yanagisawa N, Nakazato M, Tsukagoshi H. Ikeda S, et al. Among authors: nakazato m. Eur Neurol. 1992;32(6):308-13. doi: 10.1159/000116850. Eur Neurol. 1992. PMID: 1490495

5

Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy.

Nakazato M, Ikeda S, Shiomi K, Matsukura S, Yoshida K, Shimizu H, Atsumi T, Kangawa K, Matsuo H. Nakazato M, et al. FEBS Lett. 1992 Jul 20;306(2-3):206-8. doi: 10.1016/0014-5793(92)81001-3. FEBS Lett. 1992. PMID: 1633877 Free article.

6

Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy.

Nakazato M, Tanaka M, Yamamura Y, Kurihara T, Matsukura S, Kangawa K, Matsuo H. Nakazato M, et al. Arch Neurol. 1987 Dec;44(12):1275-8. doi: 10.1001/archneur.1987.00520240053011. Arch Neurol. 1987. PMID: 2823755

7

"Sporadic" prealbumin-related amyloid polyneuropathy: report of two cases.

Yamada M, Tsukagoshi H, Satoh J, Ishiai S, Nakazato M, Furuya H, Sasaki H, Sakaki Y, Yokota T. Yamada M, et al. Among authors: nakazato m. J Neurol. 1987 Dec;235(2):69-73. doi: 10.1007/BF00718012. J Neurol. 1987. PMID: 2828557

8

Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.

Tanaka M, Hirai S, Matsubara E, Okamoto K, Morimatsu M, Nakazato M. Tanaka M, et al. Among authors: nakazato m. J Neurol Neurosurg Psychiatry. 1988 Apr;51(4):576-8. doi: 10.1136/jnnp.51.4.576. J Neurol Neurosurg Psychiatry. 1988. PMID: 3379433 Free PMC article.

9

Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.

Furuya H, Yoshioka K, Sasaki H, Sakaki Y, Nakazato M, Matsuo H, Nakadai A, Ikeda S, Yanagisawa N. Furuya H, et al. Among authors: nakazato m. J Clin Invest. 1987 Dec;80(6):1706-11. doi: 10.1172/JCI113261. J Clin Invest. 1987. PMID: 3479441 Free PMC article.

10

Diagnostic value of abdominal fat tissue aspirate in familial amyloid polyneuropathy.

Maruyama K, Ikeda S, Yanagisawa N, Nakazato M. Maruyama K, et al. Among authors: nakazato m. J Neurol Sci. 1987 Oct;81(1):11-8. doi: 10.1016/0022-510x(87)90180-8. J Neurol Sci. 1987. PMID: 3681341

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