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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 1
1984 1
1987 1
1988 1
1989 1
1990 1
1991 1
1992 2
1993 3
1994 1
1995 3
1996 1
1997 1
1998 4
1999 1
2000 2
2001 2
2007 1
2013 1
2015 1
2016 1
2017 3
2018 2
2019 1
2024 0

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35 results

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Page 1
Genetic disease patterns in Japan: a review.
Fujiki N, Kohli Y, Kato T, Hirayama M, Mutoh T, Nakanaga M, Tokuda A, Nakazaki S, Dochin M, Mano K. Fujiki N, et al. Among authors: nakazaki s. Hum Biol. 1992 Dec;64(6):855-67. Hum Biol. 1992. PMID: 1427743 Review.
Hemorrhagic type moyamoya disease.
Saeki N, Nakazaki S, Kubota M, Yamaura A, Hoshi S, Sunada S, Sunami K. Saeki N, et al. Among authors: nakazaki s. Clin Neurol Neurosurg. 1997 Oct;99 Suppl 2:S196-201. doi: 10.1016/s0303-8467(97)00079-6. Clin Neurol Neurosurg. 1997. PMID: 9409437
Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations.
Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige SI, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y, Tsuji S. Mitsui J, et al. Among authors: nakazaki s. Cerebellum. 2017 Jun;16(3):664-672. doi: 10.1007/s12311-017-0846-9. Cerebellum. 2017. PMID: 28150130 Free PMC article.
35 results