Takuro Fujimaki
Kohinata, Japan
Last Updated: 09/26/2026
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Found 8 publications
Designing a muon scattering scanner for nuclear debris measurement.
Journal: Applied optics
Published: March 04, 2024
LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells.
Journal: Journal of human genetics
Published: February 15, 2018
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1.
Journal: Human mutation
Published: April 15, 2015
Epilepsy phenotypes in siblings with Norrie disease.
Journal: Brain & development
Published: February 19, 2015
A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.
Journal: Japanese journal of ophthalmology
Published: October 27, 2013
Familial cases of Norrie disease detected by copy number analysis.
Journal: Japanese journal of ophthalmology
Published: October 16, 2013
Effect of long-term treatment with eyedrops for glaucoma on conjunctival bacterial flora.
Journal: Infection and drug resistance
Published: October 19, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026