Itsuka Matsushita
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Explore the profile of Itsuka Matsushita including associated specialties, affiliations and a list of published articles.
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23
Citations
95
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Recent Articles
1.
Okamoto M, Matsushita I, Nagata T, Fujino Y, Kondo H
Ophthalmol Retina
. 2024 Aug;
9(2):187-193.
PMID: 39197492
Purpose: To determine the ultra-widefield fluorescein angiographic (UWFA) characteristics of patients with mild familial exudative vitreoretinopathy (FEVR) who had been confirmed to have pathogenic variants of the autosomal dominant (AD)...
2.
Arima M, Inoue H, Misumi A, Tsukamoto S, Matsushita I, Araki S, et al.
Jpn J Ophthalmol
. 2024 Jul;
68(5):490-499.
PMID: 39060675
Purpose: To assess the safety and efficacy of ripasudil for retinopathy of prematurity (ROP). Study Design: Phase 1/2, multicenter, open-label, single-arm, 12-week clinical trial. Methods: Infants born with gestational age...
3.
Kondo H, Tsukahara-Kawamura T, Matsushita I, Nagata T, Hayashi T, Nishina S, et al.
Ophthalmol Sci
. 2024 Jun;
4(5):100514.
PMID: 38881609
Purpose: To determine the clinical characteristics of familial exudative vitreoretinopathy (FEVR) associated with or without pathogenic variants of the Norrin/β-catenin genes. Design: This was a multicenter, cross-sectional, observational, and genetic...
4.
Dong S, Zou T, Zhen F, Wang T, Zhou Y, Wu J, et al.
Eur J Hum Genet
. 2023 Dec;
32(4):413-420.
PMID: 38052906
Congenital acorea is a rare disease with the absence of a pupil in the eye. To date, only one family and two isolated cases with congenital acorea have been reported....
5.
Nakajima A, Kuniyoshi K, Iwahashi C, Mano F, Hayashi T, Kondo H, et al.
Front Med (Lausanne)
. 2023 Nov;
10:1280564.
PMID: 38034549
Introduction: Congenital X-linked retinoschisis (XLRS) presents as macular retinoschisis/degeneration in almost all patients and as peripheral retinoschisis in half the patients. Although the optical coherence tomography (OCT) findings of macular...
6.
Morita H, Matsushita I, Fujino Y, Obana A, Kondo H
Jpn J Ophthalmol
. 2023 Nov;
68(1):19-25.
PMID: 37966565
Purpose: To develop a method to measure the macular pigment optical density (MPOD) using scanning laser ophthalmoscopic images in young adults and children. Study Design: Cross-sectional study. Methods: Blue light...
7.
Matsushita I, Izumi H, Ueno S, Hayashi T, Fujinami K, Tsunoda K, et al.
Genes (Basel)
. 2023 Jul;
14(7).
PMID: 37510387
The human fovea is a specialized pit structure in the central retina. Foveal hypoplasia is a condition where the foveal pit does not fully develop, and it is associated with...
8.
Iwahashi C, Matsushita I, Kuniyoshi K, Kondo H, Kusaka S
Retina
. 2023 Apr;
43(7):e43-e44.
PMID: 37026808
No abstract available.
9.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, et al.
Hum Mutat
. 2022 Oct;
43(12):2251-2264.
PMID: 36284460
Inherited retinal diseases (IRDs) comprise a phenotypically and genetically heterogeneous group of ocular disorders that cause visual loss via progressive retinal degeneration. Here, we report the genetic characterization of 1210...
10.
Iwahashi C, Matsushita I, Kuniyoshi K, Kondo H, Kusaka S
Retina
. 2022 Sep;
43(1):64-71.
PMID: 36165991
Purpose: To present the clinical characteristics, surgical outcomes, and surgical complications of patients with congenital X-linked retinoschisis who underwent vitrectomy for bullous schisis cavity hanging over or threatening the macula....