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ARVO Annual Meeting Abstract April 2014

A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.

Takuro Fujimaki; Takahide Suzuki; Ai Yanagawa; Eisuke Arai; Keiko Fujiki; Yuko Wada; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3284.

ARVO Annual Meeting Abstract April 2014

Partial NMNAT1 deletions cause Leber Congenital Amaurosis

Frauke Coppieters; Takuro Fujimaki; Marieke De Bruyne; Annelot Baert; Mineo Kondo; Akira Murakami; Elfride De Baere

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3285.

ARVO Annual Meeting Abstract June 2013

NMNAT1 p.Arg237Cys mutation in Japanese patients with Leber congenital amaurosis

Tomoka Kambe; Takuro Fujimaki; Shuri Kawamorita; Eisuke Arai; Ai Miyazaki; Keiko Fujiki; Fumino Iwata; Chieko Tamura; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1312.

ARVO Annual Meeting Abstract June 2013

Genetic and clinical features of FEVR and Norrie disease

Eisuke Arai; Takuro Fujimaki; Ai Miyazaki; Keiko Fujiki; Fumino Iwata; Takenori Inomata; Hiroyuki Kawano; Toshiyuki Yokoyama; Akihisa Okumura; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1331.

ARVO Annual Meeting Abstract April 2011

Developmental Abnormality Of Schlemm's Canal In Primary Open Angle Glaucoma

Teruhiko Hamanaka; Akira Matsuda; Nobuo Ishida; Takuro Fujimaki; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4668.

ARVO Annual Meeting Abstract April 2011

Genetic Analysis of Indonesian Patients with Retinitis Pigmentosa (RP)

Takuro Fujimaki; Arief S. Kartasasmita; Keiko Fujiki; Erwin Iskandar; Iwan Sovani; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5393.

ARVO Annual Meeting Abstract April 2010

Mutation Analysis of FZD4, NDP, and LRP5 in Familial Exudative Vitreoretinopathy Patients

T. Fujimaki; A. Miyazaki; N. R. Setyoningrum; K. Fujiki; T. Fujimaki; H. Kawano; F. Iwata; T. Kanbe; T. Hamahata; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2597.

ARVO Annual Meeting Abstract April 2010

A Device for Gene Transfer to the Anterior Segment of the Eye Using Anionic Hydrogel Contact Lens

T. Matsunaga; T. Sato; Y. Watanabe; T. Fujimaki; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):3114.

ARVO Annual Meeting Abstract April 2009

Gene Transfer to the Corneal Epithelial Cells Using a Hydrogel Contact Lens

T. Matsunaga; T. Sato; Y. Watanabe; H. Toshida; T. Fujimaki; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):1733.

ARVO Annual Meeting Abstract April 2009

NDP Gene Analysis for Norrie Disease Sibling

T. Fujimaki; A. Miyazaki; K. Fujiki; T. Yokoyama; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2305.

ARVO Annual Meeting Abstract May 2008

A Case Report of Oculofaciocardiodental Syndrome With Novel BCOR Gene Mutation

T. Fujimaki; T. Yokoyama; H. Kawano; K. Fujiki; M. Ikeda; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):465.

ARVO Annual Meeting Abstract May 2007

A Case of Oculo Dento Digital Dysplasia Syndrome With Novel GJA1 Gene Mutation

T. Fujimaki; M. Himi; K. Fujiki; T. Takizawa; T. Yokoyama; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):1326.

ARVO Annual Meeting Abstract May 2006

Construction of a Knock–Out Model of X–Arrestin

J.P. Marion; T. Fujimaki; H. Kitagawa; H. Sakuma; A. Murakami; Z.–Y. Huang; G. Inana

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):3730.

Glaucoma June 2005

Genetic Polymorphisms in the Angiotensin II Receptor Gene and Their Association with Open-Angle Glaucoma in a Japanese Population

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Kouhei Hashizume; Yukihiko Mashima; Tomoyo Fumayama; Yuichiro Ohtake; Itaru Kimura; Kazuhide Yoshida; Karin Ishikawa; Noriko Yasuda; Takuro Fujimaki; Ryo Asaoka; Takahisa Koga; Takashi Kanamoto; Takeo Fukuchi; Koichi Miyaki
TAGS: genes, genotype, glaucoma, intraocular pressure, japanese, open-angle glaucoma, polymorphism, receptor, angiotensin ii, angiotensin receptor antagonists
Invest. Ophthalmol. Vis. Sci.. 2005; 46(6):1993-2001. https://doi.org/10.1167/iovs.04-1100

ARVO Annual Meeting Abstract May 2005

Screening for Eyes at Risk for Angle–closure Glaucoma by Non–physician Operated Scanning Peripheral Anterior Chamber Depth Analyzer

K. Kashiwagi; T. Fujimaki; M. Tanaka; A. Nakazawa; N. Shimizu; K. Saito; N. Akaike; J. Nakayama; S. Tsukahara

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):149.

ARVO Annual Meeting Abstract May 2005

Ala363Thr Mutation in the Myocilin Gene in Japanese Glaucoma Patients

A. Ohyama; K. Fujiki; K. Kawabata; T. Kimura; T. Fujimaki; A. Murakami; Y. Mashima

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):41.

ARVO Annual Meeting Abstract May 2005

Ocular Pulse Amplitude With Normal Tension Glaucoma in Japan

K. Kawabata; T. Kimura; T. Fujimaki; A. Ohyama; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1335.

ARVO Annual Meeting Abstract May 2005

Cone–Specific Expression Driven by X–Arrestin Promoters in Transgenic Models

J.P. Marion; Z.–Y. Huang; T. Fujimaki; H. Kitagawa; H. Sakuma; A. Murakami; A. Kanai; G. Inana

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3069.

ARVO Annual Meeting Abstract May 2005

Comparative Studies in Humphrey Field Analyzer, FDT Screener and Humphrey Matrix for the Detection of Normal Tension Glaucoma

T. Kimura; K. Kawabata; A. Ohyama; S. Hasegawa; T. Fujimaki; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3722.

ARVO Annual Meeting Abstract May 2005

Lactoferrin Gene Mutation in Gelatinous Drop–like Corneal Dystrophy

T. Fujimaki; K. Fujiki; H. Toshida; A. Murakami

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4918.

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A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.

Partial NMNAT1 deletions cause Leber Congenital Amaurosis

NMNAT1 p.Arg237Cys mutation in Japanese patients with Leber congenital amaurosis

Genetic and clinical features of FEVR and Norrie disease

Developmental Abnormality Of Schlemm's Canal In Primary Open Angle Glaucoma

Genetic Analysis of Indonesian Patients with Retinitis Pigmentosa (RP)

Mutation Analysis of FZD4, NDP, and LRP5 in Familial Exudative Vitreoretinopathy Patients

A Device for Gene Transfer to the Anterior Segment of the Eye Using Anionic Hydrogel Contact Lens

Gene Transfer to the Corneal Epithelial Cells Using a Hydrogel Contact Lens

NDP Gene Analysis for Norrie Disease Sibling

A Case Report of Oculofaciocardiodental Syndrome With Novel BCOR Gene Mutation

A Case of Oculo Dento Digital Dysplasia Syndrome With Novel GJA1 Gene Mutation

Construction of a Knock–Out Model of X–Arrestin

Genetic Polymorphisms in the Angiotensin II Receptor Gene and Their Association with Open-Angle Glaucoma in a Japanese Population

Screening for Eyes at Risk for Angle–closure Glaucoma by Non–physician Operated Scanning Peripheral Anterior Chamber Depth Analyzer

Ala363Thr Mutation in the Myocilin Gene in Japanese Glaucoma Patients

Ocular Pulse Amplitude With Normal Tension Glaucoma in Japan

Cone–Specific Expression Driven by X–Arrestin Promoters in Transgenic Models

Comparative Studies in Humphrey Field Analyzer, FDT Screener and Humphrey Matrix for the Detection of Normal Tension Glaucoma

Lactoferrin Gene Mutation in Gelatinous Drop–like Corneal Dystrophy

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