Hasil Pencarian - Kaoru Fujinami

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  1. 1
    Macular Hole Associated with Vogt-Koyanagi-Harada Disease at the Acute Uveitic Stage

    Macular Hole Associated with Vogt-Koyanagi-Harada Disease at the Acute Uveitic Stage oleh Masaharu Mizuno, Kaoru Fujinami, Ken Watanabe, Kunihiko Akiyama

    Diterbitkan 2015-09-01
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  2. 2
    Multisystem Inflammatory Syndrome in Adults after Mild SARS-CoV-2 Infection, Japan

    Multisystem Inflammatory Syndrome in Adults after Mild SARS-CoV-2 Infection, Japan oleh Yasuhiro Yamada, Kaoru Fujinami, Tadashi Eguchi, Hiroshi Takefuji, Nobuaki Mori

    Diterbitkan 2021-06-01
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  3. 3
    Haptic Breakage after Transscleral Fixation of a Single-Piece Acrylic Intraocular Lens

    Haptic Breakage after Transscleral Fixation of a Single-Piece Acrylic Intraocular Lens oleh Hiroki Tanaka, Kaoru Fujinami, Ken Watanabe, Toru Noda, Kunihiko Akiyama

    Diterbitkan 2014-07-01
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  4. 4
    Advanced quantitative analysis of the sub-retinal pigment epithelial space in recurrent neovascular age-related macular degeneration.

    Advanced quantitative analysis of the sub-retinal pigment epithelial space in recurrent neovascular age-related macular degeneration. oleh Mariko Sasaki, Yu Kato, Kaoru Fujinami, Toshiaki Hirakata, Kazushige Tsunoda, Ken Watanabe, Kunihiko Akiyama, Toru Noda

    Diterbitkan 2017-01-01
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  5. 5
    Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings

    Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings oleh Kei Mizobuchi, Takaaki Hayashi, Kazutoshi Yoshitake, Kaoru Fujinami, Toshiaki Tachibana, Kazushige Tsunoda, Takeshi Iwata, Tadashi Nakano

    Diterbitkan 2020-08-01
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  6. 6
    Fish oil supplementation and repeated macular hemorrhage without choroidal neovascularization: A case report

    Fish oil supplementation and repeated macular hemorrhage without choroidal neovascularization: A case report oleh Shi-Ying Li, Kaoru Fujinami, Sheila G Crewther, Yan-Ling Long, Hong-Xuan Lie, Zheng-Qin Yin

    Diterbitkan 2020-09-01
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  7. 7
    Gene Therapy for Inherited Retinal Diseases: From Laboratory Bench to Patient Bedside and Beyond

    Gene Therapy for Inherited Retinal Diseases: From Laboratory Bench to Patient Bedside and Beyond oleh Anand Singh Brar, Deepika C. Parameswarappa, Brijesh Takkar, Raja Narayanan, Subhadra Jalali, Sohini Mandal, Kaoru Fujinami, Srikanta Kumar Padhy

    Diterbitkan 2023-12-01
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  8. 8
    A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder

    A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder oleh Kazuki Yamazawa, Kenji Shimizu, Hirofumi Ohashi, Hidenori Haruna, Satomi Inoue, Haruka Murakami, Tatsuo Matsunaga, Takeshi Iwata, Kazushige Tsunoda, Kaoru Fujinami

    Diterbitkan 2021-12-01
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  9. 9
    Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X)

    Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X) oleh Kei Mizobuchi, Satoshi Katagiri, Takaaki Hayashi, Kazutoshi Yoshitake, Kaoru Fujinami, Kazuki Kuniyoshi, Reimi Mishima, Kazushige Tsunoda, Takeshi Iwata, Tadashi Nakano

    Diterbitkan 2019-03-01
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  10. 10
    Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques

    Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques oleh Yu Fujinami-Yokokawa, Nikolas Pontikos, Lizhu Yang, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Hiroaki Miyata, Kaoru Fujinami, on behalf of Japan Eye Genetics Consortium

    Diterbitkan 2019-01-01
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  11. 11
    Phenogenon: Gene to phenotype associations for rare genetic diseases.

    Phenogenon: Gene to phenotype associations for rare genetic diseases. oleh Nikolas Pontikos, Cian Murphy, Ismail Moghul, Gavin Arno, Kaoru Fujinami, Yu Fujinami, Dayyanah Sumodhee, Susan Downes, Andrew Webster, Jing Yu, UK Inherited Retinal Dystrophy Consortium, Phenopolis Consortium

    Diterbitkan 2020-01-01
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  12. 12
    Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with <i>DRAM2</i>-Associated Retinopathy

    Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with <i>DRAM2</i>-Associated Retinopathy oleh Kazuki Kuniyoshi, Takaaki Hayashi, Shuhei Kameya, Satoshi Katagiri, Kei Mizobuchi, Toshiaki Tachibana, Daiki Kubota, Hiroyuki Sakuramoto, Kazushige Tsunoda, Kaoru Fujinami, Kazutoshi Yoshitake, Takeshi Iwata, Tadashi Nakano, Shunji Kusaka

    Diterbitkan 2020-02-01
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  13. 13
    Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review

    Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review oleh Howard Maile, Ji-Peng Olivia Li, Daniel Gore, Marcello Leucci, Padraig Mulholland, Scott Hau, Anita Szabo, Ismail Moghul, Konstantinos Balaskas, Kaoru Fujinami, Pirro Hysi, Alice Davidson, Petra Liskova, Alison Hardcastle, Stephen Tuft, Nikolas Pontikos

    Diterbitkan 2021-12-01
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  14. 14
    Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)

    Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene) oleh Sagnik Sen, Michel Michaelides, Andrew R Webster, Konstantinos Balaskas, Kaoru Fujinami, Manuel Gomes, Nikolas Pontikos, Susan M Downes, Malena Daich Varela, Omar A Mahroo, Thales Antonio Cabral de Guimaraes, Stephen Archer, Gavin Arno, Mital Shah, Savita Madhusudhan, Quang Nguyen, William Woof, Nathaniel Kabiri, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Jennifer Furman

    Diterbitkan 2023-03-01
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  15. 15
    Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes

    Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes oleh Rebekkah J. Hitti-Malin, Daan M. Panneman, Zelia Corradi, Erica G. M. Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard H. F. Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Sandro Banfi, Tamar Ben-Yosef, Damjan Glavač, G. Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P. Szaflik, Anna Matynia, Michael B. Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfride De Baere, Carel B. Hoyng, Catherina H. Z. Li, Caroline C. W. Klaver, Chris F. Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L. Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L. Vincent, Lisa Roberts, Raj Ramesar, Giovanna Sartor, Elena Luppi, Susan M. Downes, L. Ingeborgh van den Born, Terri L. McLaren, John N. De Roach, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, Anna M. Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J. Bolz, Hülya Kayserili, Susanne Roosing, Frans P. M. Cremers

    Diterbitkan 2024-03-01
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