Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Kiyoko, Gocho"'
Autor:
Marie Elise Wistrup Torm, Michael Pircher, Sophie Bonnin, Jesper Johannesen, Oliver Niels Klefter, Mathias Falck Schmidt, Jette Lautrup Frederiksen, Nicolas Lefaudeux, Jordi Andilla, Claudia Valdes, Pablo Loza-Alvarez, Luisa Sanchez Brea, Danilo Andrade De Jesus, Kate Grieve, Michel Paques, Michael Larsen, Kiyoko Gocho
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract This study tested if a high-resolution, multi-modal, multi-scale retinal imaging instrument can provide novel information about structural abnormalities in vivo. The study examined 11 patients with very mild to moderate non-proliferative dia
Externí odkaz:
https://doaj.org/article/676c9439b8bc439bab580766c1c33eea
Publikováno v:
Frontiers in Ophthalmology, Vol 4 (2024)
Externí odkaz:
https://doaj.org/article/ca920e2b1c2a45b0a3bdaaac9972db8f
Autor:
Shohei Kitahata, Kiyoko Gocho, Naohiro Motozawa, Satoshi Yokota, Midori Yamamoto, Akiko Maeda, Yasuhiko Hirami, Yasuo Kurimoto, Kazuaki Kadonosono, Masayo Takahashi
Publikováno v:
PLoS ONE, Vol 19, Iss 1, p e0296493 (2024)
ObjectiveCystoid macular edema (CME) in retinitis pigmentosa (RP) is an important complication causing visual dysfunction. We investigated the effect of CME on photoreceptors in RP patients with previous or current CME, using an adaptive optics (AO)
Externí odkaz:
https://doaj.org/article/c0fbdb85af0a4ad19d6b97e114e475f7
Autor:
Elena Gofas-Salas, Daniel M. W. Lee, Christophe Rondeau, Kate Grieve, Ethan A. Rossi, Michel Paques, Kiyoko Gocho
Publikováno v:
Diagnostics, Vol 14, Iss 7, p 768 (2024)
The Retinal Pigment Epithelium (RPE) plays a prominent role in diseases such as age-related macular degeneration, but imaging individual RPE cells is challenging due to their high absorption and low autofluorescence emission. The RPE lies beneath the
Externí odkaz:
https://doaj.org/article/c36ae76fe90a43a58493a8bc0c078ddc
Autor:
Muhammad Faizan Shirazi, Jordi Andilla, Nicolas Lefaudeux, Claudia Valdes, Florian Schwarzhans, Marine Durand, Konstantinos Ntatsis, Danilo Andrade De Jesus, Luisa Sanchez Brea, Kiyoko Gocho, Josselin Gautier, Christina Eckmann-Hansen, Marie Elise Wistrup Torm, Abdullah Amini, Stefan Klein, Theo Van Walsum, Kate Grieve, Michel Paques, Michael Larsen, Pablo Loza-Alvarez, Xavier Levecq, Nicolas Chateau, Michael Pircher
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract We present a compact multi-modal and multi-scale retinal imaging instrument with an angiographic functional extension for clinical use. The system integrates scanning laser ophthalmoscopy (SLO), optical coherence tomography (OCT) and OCT ang
Externí odkaz:
https://doaj.org/article/12a6fc229709437998872823e2734a27
Publikováno v:
Frontiers in Ophthalmology; 2024, p1-3, 3p
Autor:
Daiki Kubota, Kunihiko Yamaki, Shuhei Kameya, Tsutomu Igarashi, Kaori Maruyama, Noriko Oishi, Kiyoko Gocho, Yukito Takeda, Hiroshi Takahashi
Publikováno v:
Journal of Nippon Medical School. 87:92-99
Background The GUCY2D (guanylate cyclase 2D) gene encodes a photoreceptor guanylate cyclase (GC-E), that is predominantly expressed in the cone outer segments. Mutations in the GUCY2D lead to severe retinal disorders such as autosomal dominant cone-r
Autor:
Takeda, Yukito, Kubota, Daiki, Oishi, Noriko, Maruyama, Kaori, Gocho, Kiyoko, Yamaki, Kunihiko, Igarashi, Tsutomu, Takahashi, Hiroshi, Yukito, Takeda, Daiki, Kubota, Noriko, Oishi, Kaori, Maruyama, Kiyoko, Gocho, Kunihiko, Yamaki, Tsutomu, Igarashi, Hiroshi, Takahashi, Shuhei, Kameya
Publikováno v:
Journal of Nippon Medical School. 87(2):92-99
The GUCY2D (guanylate cyclase 2D) gene encodes a photoreceptor guanylate cyclase (GC-E), that is predominantly expressed in the cone outer segments. Mutations in the GUCY2D lead to severe retinal disorders such as autosomal dominant cone-rod dystroph
Autor:
Keiichiro Akeo, Shuhei Kameya, Kiyoko Gocho, Daiki Kubota, Kunihiko Yamaki, Hiroshi Takahashi
Publikováno v:
Case Reports in Ophthalmological Medicine, Vol 2015 (2015)
Purpose. To report the morphological and functional changes associated with a regression of foveoschisis in a patient with X-linked retinoschisis (XLRS). Methods. A 42-year-old man with XLRS underwent genetic analysis and detailed ophthalmic examinat
Externí odkaz:
https://doaj.org/article/26a9ef69fc5d4f0d9cc191d56dd4eef0
Autor:
Kiyoko Gocho, Daiki Kubota, Hiroshi Takahashi, Noriko Oishi, Atsushi Mizota, Tsutomu Igarashi, Takeshi Iwata, Shuhei Kameya, Nobuo Ishida, Sachiko Kikuchi, Kunihiko Yamaki
Publikováno v:
Ophthalmic Genetics. 40:480-487
Background: The GNAT1 gene encodes the alpha-subunit of transducin in rod photoreceptors and is an important part of the phototransduction cascade. Defects in GNAT1 are very rare but have been identified in autosomal dominant and recessive congenital