Detalhe da pesquisa
1.
Siblings with optic neuropathy and RTN4IP1 mutation.
J Hum Genet
; 62(10): 927-929, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28638143
2.
Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.
Doc Ophthalmol
; 130(1): 49-55, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25323024
3.
Continuous oxygen saturation and risk of retinopathy of prematurity in a Japanese cohort.
Br J Ophthalmol
; 2024 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38448200
4.
Ophthalmic features of CHARGE syndrome with CHD7 mutations.
Am J Med Genet A
; 158A(3): 514-8, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22302456
5.
Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in NMNAT1: a case report and mini review.
Ophthalmic Genet
; 43(3): 400-408, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35026968
6.
Submicroscopic deletion in 7q31 encompassing CADPS2 and TSPAN12 in a child with autism spectrum disorder and PHPV.
Am J Med Genet A
; 155A(7): 1568-73, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21626674
7.
[Surgical results of unilateral recession-resection for intermittent exotropia in children: multicenter study in Japan].
Nippon Ganka Gakkai Zasshi
; 115(5): 440-6, 2011 May.
Artigo
em Japonês
| MEDLINE | ID: mdl-21706837
8.
Characterization of the Progression Pattern in Retinopathy of Prematurity Subtypes.
Ophthalmol Retina
; 4(3): 231-237, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31982389
9.
Effect of fluctuation of oxygenation on the development of severe retinopathy of prematurity in extremely preterm infants.
J Perinatol
; 40(3): 515-521, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907394
10.
Retrospective Validation of the Postnatal Growth and Retinopathy of Prematurity (G-ROP) Criteria in a Japanese Cohort.
Am J Ophthalmol
; 205: 50-53, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30954468
11.
Progression and timing of treatment of zone I retinopathy of prematurity.
Am J Ophthalmol
; 146(3): 369-374, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18602081
12.
Favorable outcomes of adequate laser photocoagulation and salvage bevacizumab treatment for aggressive posterior retinopathy of prematurity.
Am J Ophthalmol Case Rep
; 11: 66-71, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29998205
13.
Abnormal retinal blood vessels in Ehlers-Danlos syndrome type VI.
Jpn J Ophthalmol
; 51(6): 453-5, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-18158597
14.
Endocrine status of patients with septo-optic dysplasia: fourteen Japanese cases.
Clin Pediatr Endocrinol
; 26(2): 89-98, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28458461
15.
Acute Bilateral Photoreceptor Degeneration in an Infant After Vaccination Against Measles and Rubella.
JAMA Ophthalmol
; 135(5): 478-482, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28358967
16.
The effect of early treatment at the initial stage 3 moderate phase of retinopathy of prematurity on severe retinal changes.
Jpn J Ophthalmol
; 49(5): 391-6, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16187040
17.
[Retinopathy of prematurity: to intensify the neonatal eye care system].
Nippon Ganka Gakkai Zasshi
; 114(4): 343-5, 2010 Apr.
Artigo
em Japonês
| MEDLINE | ID: mdl-20432958
18.
Congenital optic tract hypoplasia.
J AAPOS
; 19(4): 383-5, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26228965
19.
Changes in angle of optic nerve and angle of ocular orbit with increasing age in Japanese children.
Br J Ophthalmol
; 99(2): 263-6, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25147368
20.
Deep intronic GPR143 mutation in a Japanese family with ocular albinism.
Sci Rep
; 5: 11334, 2015 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26061757