Detalhe da pesquisa
1.
Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
Doc Ophthalmol
; 132(3): 233-43, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27071392
2.
Multimodal imaging of a case of peripheral cone dystrophy.
Doc Ophthalmol
; 130(3): 241-51, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25708979
3.
An effective strategy to reduce blood pressure after forest walking in middle-aged and aged people.
J Phys Ther Sci
; 27(12): 3711-6, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26834337
4.
Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families.
Sci Rep
; 10(1): 15883, 2020 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32985515
5.
Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family.
Ophthalmic Genet
; 40(5): 480-487, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31696758
6.
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia.
Ophthalmic Surg Lasers Imaging Retina
; 50(2): 76-85, 2019 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30768214
7.
Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance.
Invest Ophthalmol Vis Sci
; 60(10): 3432-3446, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31390656
8.
New values of molecular extinction coefficient and specific rotation for cyanobacterial toxin cylindrospermopsin.
Toxicon
; 51(4): 717-9, 2008 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18187178
9.
Case of Sweet's syndrome with extensive necrosis and ulcers accompanied by myelodysplastic syndrome.
J Nippon Med Sch
; 75(3): 162-5, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18648174
10.
CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family.
Ophthalmic Genet
; 39(4): 500-507, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29718797
11.
Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variants.
Ophthalmic Genet
; 39(2): 255-262, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220607
12.
Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy.
Invest Ophthalmol Vis Sci
; 57(11): 4837-46, 2016 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27623337
13.
Cone dystrophy in patient with homozygous RP1L1 mutation.
Biomed Res Int
; 2015: 545243, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25692141
14.
High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation.
J Ophthalmol
; 2014: 283603, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25276414
15.
High-resolution en face images of microcystic macular edema in patients with autosomal dominant optic atrophy.
Biomed Res Int
; 2013: 676803, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24369534
16.
Closure of a full-thickness macular hole without vitrectomy in choroideraemia.
Clin Exp Optom
; 100(3): 294-295, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27628750
17.
Cylindrospermopsin determination using 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES) as the internal standard.
Anal Chim Acta
; 583(1): 124-7, 2007 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-17386536
18.
Limbal nodules associated with Sweet's syndrome.
Jpn J Ophthalmol
; 53(6): 652-653, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20020248