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Japanese Journal of Ophthalmology|May 9, 2012
Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmosItsuka Matsushita, Hiroyuki Kondo, Akihiko Tawara
Japanese Journal of Ophthalmology|August 29, 2020
Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutationsItsuka Matsushita, Hirofumi Morita, Hiroyuki Kondo
Retina (Philadelphia, Pa.)|September 15, 2025
Excision of extensive subretinal fibrosis associated with rhegmatogenous retinal detachments in patients with familial exudative vitreoretinopathyHiroyuki Kondo, Itsuka Matsushita, Mizuki Tsurusaki
Japanese Journal of Ophthalmology|November 15, 2023
Measuring macular pigment optical density using reflective images of confocal scanning laser systemHirofumi Morita, Itsuka Matsushita, Yoshihisa Fujino, et al.
Retina (Philadelphia, Pa.)|September 27, 2022
EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISISChiharu Iwahashi, Itsuka Matsushita, Kazuki Kuniyoshi, et al.
Ophthalmology. Retina|August 28, 2024
Angiographic Characteristics in Mild Familial Exudative Vitreoretinopathy with Genetically Confirmed Autosomal Dominant InheritanceMisato Okamoto, Itsuka Matsushita, Tatsuo Nagata, et al.
Scientific Reports|September 30, 2021
Vitrectomy and external drainage of subretinal fluid containing high concentration of vascular endothelial growth factor for advanced coats diseaseFukutaro Mano, Itsuka Matsushita, Hiroyuki Kondo, et al.
Ophthalmic Genetics|April 27, 2022
Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in <i>COL2A1</i> geneMamika Asano, Katsuhiko Yokoyama, Kazuma Oku, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 30, 2019
Electroretinograms of eyes with Stickler syndromeHiroyuki Kondo, Kazushi Fujimoto, Mamika Imagawa, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 26, 2021
Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case reportTakaaki Hayashi, Hiroyuki Kondo, Itsuka Matsushita, et al.
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