Detalhe da pesquisa
1.
The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients.
Int J Mol Sci
; 24(18)2023 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37761981
2.
The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.
J Hum Genet
; 59(9): 521-8, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25078356
3.
Interaction between optineurin and the bZIP transcription factor NRL.
Cell Biol Int
; 38(1): 16-25, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23956131
4.
Intraocular pressure changes at different gaze positions after superior rectus muscle-lateral rectus muscle loop myopexy in highly myopic strabismus.
Jpn J Ophthalmol
; 68(1): 26-31, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37966564
5.
Recovery of stereoacuity after Yokoyama procedure in patients with highly myopic strabismus with good vision.
Am J Ophthalmol Case Rep
; 32: 101892, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37484135
6.
A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants.
Ophthalmic Genet
; 44(5): 480-485, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341712
7.
Clinical presentations of acquired comitant esotropia in 5-35 years old Japanese and digital device usage: a multicenter registry data analysis study.
Jpn J Ophthalmol
; 67(6): 629-636, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37695434
8.
Medial Rectus Muscle Resection Versus Plication: A Comparison of Conjunctival-Scleral Thickness Measured by AS-OCT.
J Pediatr Ophthalmol Strabismus
; 59(4): 274-278, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35192382
9.
Clinical findings of acute acquired comitant esotropia in young patients.
Jpn J Ophthalmol
; 66(1): 87-93, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34655005
10.
Exophthalmos associated with chronic progressive external ophthalmoplegia.
Jpn J Ophthalmol
; 66(3): 314-319, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35438395
11.
Intraocular pressure at different gaze positions in patients with highly myopic strabismus.
Jpn J Ophthalmol
; 66(6): 572-578, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36083359
12.
Two cases of acquired bilateral trochlea nerve palsy treated by simultaneous inferior rectus muscle nasal transposition and inferior oblique muscle myectomy.
Am J Ophthalmol Case Rep
; 21: 101011, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33532662
13.
Effects of the Gaze Fixation Position on AS-OCT Measurements of the Limbus and Extraocular Muscle Insertion Site Distance.
J Pediatr Ophthalmol Strabismus
; 58(1): 28-33, 2021 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495795
14.
Usefulness of handheld electroretinogram system for diagnosing blue-cone monochromatism in children.
Jpn J Ophthalmol
; 65(1): 23-29, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33135089
15.
Magnetic resonance imaging of the medial rectus muscle of patients with consecutive exotropia after medial rectus muscle recession.
Ophthalmology
; 117(10): 1876-82, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541264
16.
A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation.
Ophthalmic Genet
; 41(2): 175-182, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32223580
17.
Superior oblique palsy with class III tendon anomaly.
Am J Ophthalmol
; 146(3): 385-394, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18621358
18.
Changes in conjunctival-scleral thickness after strabismus surgery measured with anterior segment optical coherence tomography.
Jpn J Ophthalmol
; 62(5): 554-559, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29980870
19.
Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.
Jpn J Ophthalmol
; 62(4): 458-466, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29666954
20.
Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations.
Semin Ophthalmol
; 33(4): 560-565, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-28678594