Detalhe da pesquisa
1.
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Hum Mutat
; 43(12): 2251-2264, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36284460
2.
The Prevalence of Brain Abnormalities in Japanese Patients with Optic Nerve Hypoplasia.
Neuroophthalmology
; 45(4): 265-270, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34366515
3.
Clinicopathological features in anterior visual pathway in neuromyelitis optica.
Ann Neurol
; 79(4): 605-24, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26836302
4.
Dominant mutations in RP1L1 are responsible for occult macular dystrophy.
Am J Hum Genet
; 87(3): 424-9, 2010 Sep 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-20826268
5.
Molecular characteristics of four Japanese cases with KCNV2 retinopathy: report of novel disease-causing variants.
Mol Vis
; 19: 1580-90, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23885164
6.
[Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram].
Nippon Ganka Gakkai Zasshi
; 117(8): 629-40, 2013 Aug.
Artigo
em Japonês
| MEDLINE | ID: mdl-24063160
7.
One-year recurrence rate of Graves ophthalmopathy presenting as diplopia in the primary position after varied doses of intravenous methylprednisolone followed by oral prednisolone with dosing based on the magnetic resonance imaging findings.
Jpn J Ophthalmol
; 67(1): 91-96, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36301447
8.
Clinical characteristics of occult macular dystrophy in family with mutation of RP1l1 gene.
Retina
; 32(6): 1135-47, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22466457
9.
Iridocorneal contact as a potential cause of corneal decompensation following laser peripheral iridotomy.
Jpn J Ophthalmol
; 65(4): 460-471, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33728544
10.
Visual outcome of aquaporin-4 antibody-positive optic neuritis with maintenance therapy.
Jpn J Ophthalmol
; 65(5): 699-703, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34279748
11.
Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings.
Invest Ophthalmol Vis Sci
; 60(14): 4691-4700, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31725168
12.
Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular Dystrophy.
Invest Ophthalmol Vis Sci
; 58(14): 6020-6029, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29196766
13.
[Multifocal visually evoked responses in two children with optic neuritis].
Nippon Ganka Gakkai Zasshi
; 109(8): 497-503, 2005 Aug.
Artigo
em Japonês
| MEDLINE | ID: mdl-16164233
14.
Early morphological recovery of the optic chiasm is associated with excellent visual outcome in patients with compressive chiasmal syndrome caused by pituitary tumors.
Neurol Res
; 37(1): 1-8, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24938320
15.
Superior segmental optic nerve hypoplasia in youth.
Jpn J Ophthalmol
; 52(6): 468-474, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19089568