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Tomokazu Takeuchi

Showing results (1-10 of 26) with videos related to

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Nihon Hoshasen Gijutsu Gakkai Zasshi|July 23, 2019
[Verification of "IEC 62464-12007": The Evaluation Method of Spatial Resolution in MRI]Tomokazu Takeuchi, Akio Ogura, Ryosuke Shiina, et al.
Nihon Hoshasen Gijutsu Gakkai Zasshi|December 24, 2019
[Setting Method of the Optimal Slab of Brain MRA for Detective Unruptured Cerebral Aneurysm]Hiroki Nakano, Akio Ogura, Tomokazu Takeuchi, et al.
Nihon Hoshasen Gijutsu Gakkai Zasshi|May 21, 2019
[Improvement of Fat Suppressing Effect for Finger and Neck MRI by Using Small Glass Beads]Ryosuke Shiina, Akio Ogura, Tomokazu Takeuchi, et al.
Ophthalmic Research|July 12, 2005
Dominant optic atrophy caused by a novel OPA1 splice site mutation (IVS20+1G-->A) associated with intron retentionTakaaki Hayashi, Tamaki Gekka, Satoshi Omoto, et al.
Ophthalmic Genetics|September 17, 2004
Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R)Satoshi Omoto, Takaaki Hayashi, Kenji Kitahara, et al.
Physical and Engineering Sciences in Medicine|March 1, 2022
Novel method for evaluating spatial resolution of magnetic resonance imagesTomokazu Takeuchi, Norio Hayashi, Yuta Asai, et al.
Ophthalmology|October 31, 2006
A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responsesTakaaki Hayashi, Tamaki Gekka, Tomokazu Takeuchi, et al.
Ophthalmic Research|August 10, 2005
CYP4V2 mutations in two Japanese patients with Bietti's crystalline dystrophyTamaki Gekka, Takaaki Hayashi, Tomokazu Takeuchi, et al.
Investigative Ophthalmology & Visual Science|October 24, 2009
A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese familyTomokazu Takeuchi, Takaaki Hayashi, Matthew Bedell, et al.
American Journal of Ophthalmology|November 9, 2004
Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 geneTakaaki Hayashi, Satoshi Omoto, Tomokazu Takeuchi, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Nihon Hoshasen Gijutsu Gakkai Zasshi|July 23, 2019
[Verification of "IEC 62464-12007": The Evaluation Method of Spatial Resolution in MRI]Tomokazu Takeuchi, Akio Ogura, Ryosuke Shiina, et al.
Nihon Hoshasen Gijutsu Gakkai Zasshi|December 24, 2019
[Setting Method of the Optimal Slab of Brain MRA for Detective Unruptured Cerebral Aneurysm]Hiroki Nakano, Akio Ogura, Tomokazu Takeuchi, et al.
Nihon Hoshasen Gijutsu Gakkai Zasshi|May 21, 2019
[Improvement of Fat Suppressing Effect for Finger and Neck MRI by Using Small Glass Beads]Ryosuke Shiina, Akio Ogura, Tomokazu Takeuchi, et al.
Ophthalmic Research|July 12, 2005
Dominant optic atrophy caused by a novel OPA1 splice site mutation (IVS20+1G-->A) associated with intron retentionTakaaki Hayashi, Tamaki Gekka, Satoshi Omoto, et al.
Ophthalmic Genetics|September 17, 2004
Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R)Satoshi Omoto, Takaaki Hayashi, Kenji Kitahara, et al.
Physical and Engineering Sciences in Medicine|March 1, 2022
Novel method for evaluating spatial resolution of magnetic resonance imagesTomokazu Takeuchi, Norio Hayashi, Yuta Asai, et al.
Ophthalmology|October 31, 2006
A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responsesTakaaki Hayashi, Tamaki Gekka, Tomokazu Takeuchi, et al.
Ophthalmic Research|August 10, 2005
CYP4V2 mutations in two Japanese patients with Bietti's crystalline dystrophyTamaki Gekka, Takaaki Hayashi, Tomokazu Takeuchi, et al.
Investigative Ophthalmology & Visual Science|October 24, 2009
A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese familyTomokazu Takeuchi, Takaaki Hayashi, Matthew Bedell, et al.
American Journal of Ophthalmology|November 9, 2004
Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 geneTakaaki Hayashi, Satoshi Omoto, Tomokazu Takeuchi, et al.
Pageof 3