Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Yasuyuki Suzuki

Medical Education Development Center

Gifu University School of Medicine

Yanagido 1-1

Gifu 501-1194

Japan

[email]@cc.gifu-u.ac.jp

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Affiliations

Medical Education Development Center, Gifu University School of Medicine, Yanagido 1-1, Gifu 501-1194, Japan. 2005
Department of Pediatrics, Gifu University School of Medicine, Japan. 1997 - 2001

References

Natural history of X-linked adrenoleukodystrophy in Japan. Suzuki, Y., Takemoto, Y., Shimozawa, N., Imanaka, T., Kato, S., Furuya, H., Kaga, M., Kato, K., Hashimoto, N., Onodera, O., Tsuji, S. Brain Dev. (2005) [Pubmed]
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders. Suzuki, Y., Shimozawa, N., Imamura, A., Fukuda, S., Zhang, Z., Orii, T., Kondo, N. J. Inherit. Metab. Dis. (2001) [Pubmed]
Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy. Suzuki, Y., Isogai, K., Teramoto, T., Tashita, H., Shimozawa, N., Nishimura, M., Asano, T., Oda, M., Kamei, A., Ishiguro, H., Kato, S., Ohashi, T., Kobayashi, H., Eto, Y., Kondo, N. J. Inherit. Metab. Dis. (2000) [Pubmed]
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency. Suzuki, Y., Zhang, Z., Shimozawa, N., Muro, M., Shono, H., Toda, S., Miyahara, S., Hashimoto, T., Usuda, N., Ito, M., Takashima, S., Kondo, N. J. Hum. Genet. (1999) [Pubmed]
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. Suzuki, Y., Jiang, L.L., Souri, M., Miyazawa, S., Fukuda, S., Zhang, Z., Une, M., Shimozawa, N., Kondo, N., Orii, T., Hashimoto, T. Am. J. Hum. Genet. (1997) [Pubmed]
Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells. Suzuki, Y., Lee, K., Shimozawa, N., Orii, T., Kondo, N. Cell Struct. Funct. (1997) [Pubmed]

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