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Nobuo Fuse

Department of Ophthalmology

Tohoku University Graduate School of Medicine

Sendai

Miyagi

Japan

[email]@oph.med.tohoku.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan. 2004 - 2011

References

  1. Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration. Fuse, N., Mengkegale, M., Miyazawa, A., Abe, T., Nakazawa, T., Wakusawa, R., Nishida, K. Am. J. Ophthalmol. (2011) [Pubmed]
  2. Mutation spectrum of the CYP1B1 gene for congenital glaucoma in the Japanese population. Fuse, N., Miyazawa, A., Takahashi, K., Noro, M., Nakazawa, T., Nishida, K. Jpn. J. Ophthalmol. (2010) [Pubmed]
  3. Genetic bases for glaucoma. Fuse, N. Tohoku J. Exp. Med. (2010) [Pubmed]
  4. Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese. Fuse, N., Miyazawa, A., Nakazawa, T., Mengkegale, M., Otomo, T., Nishida, K. Mol. Vis. (2008) [Pubmed]
  5. Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome. Fuse, N., Takahashi, K., Yokokura, S., Nishida, K. Mol. Vis. (2007) [Pubmed]
  6. Polymorphisms in Complement Factor H and Hemicentin-1 genes in a Japanese population with dry-type age-related macular degeneration. Fuse, N., Miyazawa, A., Mengkegale, M., Yoshida, M., Wakusawa, R., Abe, T., Tamai, M. Am. J. Ophthalmol. (2006) [Pubmed]
  7. Molecular genetic analysis of optineurin gene for primary open-angle and normal tension glaucoma in the Japanese population. Fuse, N., Takahashi, K., Akiyama, H., Nakazawa, T., Seimiya, M., Kuwahara, S., Tamai, M. J. Glaucoma (2004) [Pubmed]
 
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