Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 161

1.

Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies.

Mizobuchi K, Hayashi T, Katagiri S, Yoshitake K, Fujinami K, Yang L, Kuniyoshi K, Shinoda K, Machida S, Kondo M, Ueno S, Terasaki H, Matsuura T, Tsunoda K, Iwata T, Nakano T.

Sci Rep. 2019 Nov 14;9(1):16851. doi: 10.1038/s41598-019-52660-1.

2.

Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings.

Nakamura N, Tsunoda K, Mizuno Y, Usui T, Hatase T, Ueno S, Kuniyoshi K, Hayashi T, Katagiri S, Kondo M, Kameya S, Yoshitake K, Fujinami K, Iwata T, Miyake Y.

Invest Ophthalmol Vis Sci. 2019 Nov 1;60(14):4691-4700. doi: 10.1167/iovs.19-27486.

PMID:
31725168
3.

GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel Therapies.

Bouzia Z, Georgiou M, Hull S, Robson AG, Fujinami K, Rotsos T, Pontikos N, Arno G, Webster AR, Hardcastle AJ, Fiorentino A, Michaelides M.

Am J Ophthalmol. 2019 Nov 5. pii: S0002-9394(19)30515-X. doi: 10.1016/j.ajo.2019.10.019. [Epub ahead of print]

4.

Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.

Maeda-Katahira A, Nakamura N, Hayashi T, Katagiri S, Shimizu S, Ohde H, Matsunaga T, Kaga K, Nakano T, Kameya S, Matsuura T, Fujinami K, Iwata T, Tsunoda K.

Mol Vis. 2019 Oct 5;25:559-573. eCollection 2019.

5.

Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants.

Mawatari G, Fujinami K, Liu X, Yang L, Yokokawa YF, Komori S, Ueno S, Terasaki H, Katagiri S, Hayashi T, Kuniyoshi K, Miyake Y, Tsunoda K, Yoshitake K, Iwata T, Nao-I N; JEGC study group.

Hum Genome Var. 2019 Aug 2;6:34. doi: 10.1038/s41439-019-0065-7. eCollection 2019.

6.

Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance.

Kameya S, Fujinami K, Ueno S, Hayashi T, Kuniyoshi K, Ideta R, Kikuchi S, Kubota D, Yoshitake K, Katagiri S, Sakuramoto H, Kominami T, Terasaki H, Yang L, Fujinami-Yokokawa Y, Liu X, Arno G, Pontikos N, Miyake Y, Iwata T, Tsunoda K; Japan Eye Genetics Consortium.

Invest Ophthalmol Vis Sci. 2019 Aug 1;60(10):3432-3446. doi: 10.1167/iovs.19-26650.

PMID:
31390656
7.

Late-onset night blindness with peripheral flecks accompanied by progressive trickle-like macular degeneration.

Tsunoda K, Fujinami K, Yoshitake K, Iwata T.

Doc Ophthalmol. 2019 Dec;139(3):171-184. doi: 10.1007/s10633-019-09705-7. Epub 2019 Jul 8.

PMID:
31286363
8.
9.

Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques.

Fujinami-Yokokawa Y, Pontikos N, Yang L, Tsunoda K, Yoshitake K, Iwata T, Miyata H, Fujinami K, Japan Eye Genetics Consortium OBO.

J Ophthalmol. 2019 Apr 9;2019:1691064. doi: 10.1155/2019/1691064. eCollection 2019.

10.

Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1.

Fujinami K, Yang L, Joo K, Tsunoda K, Kameya S, Hanazono G, Fujinami-Yokokawa Y, Arno G, Kondo M, Nakamura N, Kurihara T, Tsubota K, Zou X, Li H, Park KH, Iwata T, Miyake Y, Woo SJ, Sui R; East Asia Inherited Retinal Disease Society study group.

Ophthalmology. 2019 Oct;126(10):1432-1444. doi: 10.1016/j.ophtha.2019.04.032. Epub 2019 Apr 25.

11.

Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt Disease.

Tanna P, Georgiou M, Strauss RW, Ali N, Kumaran N, Kalitzeos A, Fujinami K, Michaelides M.

Transl Vis Sci Technol. 2019 Mar 1;8(2):1. doi: 10.1167/tvst.8.2.1. eCollection 2019 Mar.

12.

Estimating Visibility of Annotations for View Management in Spatial Augmented Reality Based on Machine-Learning Techniques.

Ichihashi K, Fujinami K.

Sensors (Basel). 2019 Feb 22;19(4). pii: E939. doi: 10.3390/s19040939.

13.

High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia.

Suzuki K, Gocho K, Akeo K, Kikuchi S, Kubota D, Katagiri S, Fujinami K, Tsunoda K, Iwata T, Yamaki K, Igarashi T, Nakano T, Takahashi H, Hayashi T, Kameya S.

Ophthalmic Surg Lasers Imaging Retina. 2019 Feb 1;50(2):76-85. doi: 10.3928/23258160-20190129-03.

PMID:
30768214
14.

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.

Kondo H, Oku K, Katagiri S, Hayashi T, Nakano T, Iwata A, Kuniyoshi K, Kusaka S, Hiyoshi A, Uchio E, Kondo M, Oishi N, Kameya S, Mizota A, Naoi N, Ueno S, Terasaki H, Morimoto T, Iwaki M, Yoshitake K, Iejima D, Fujinami K, Tsunoda K, Shinoda K, Iwata T.

Hum Genome Var. 2019 Jan 8;6:3. doi: 10.1038/s41439-018-0034-6. eCollection 2019.

15.

Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X).

Mizobuchi K, Katagiri S, Hayashi T, Yoshitake K, Fujinami K, Kuniyoshi K, Mishima R, Tsunoda K, Iwata T, Nakano T.

Am J Ophthalmol Case Rep. 2018 Dec 19;13:110-115. doi: 10.1016/j.ajoc.2018.12.019. eCollection 2019 Mar.

16.

Three cases of acute-onset bilateral photophobia.

Ueno S, Inooka D, Meinert M, Ito Y, Tsunoda K, Fujinami K, Iwata T, Ohde H, Terasaki H.

Jpn J Ophthalmol. 2019 Mar;63(2):172-180. doi: 10.1007/s10384-018-00649-0. Epub 2019 Jan 2.

PMID:
30604114
17.

CHANGES OF CONE PHOTORECEPTOR MOSAIC IN AUTOSOMAL RECESSIVE BESTROPHINOPATHY.

Nakanishi A, Ueno S, Hayashi T, Katagiri S, Ito Y, Kominami T, Fujinami K, Tsunoda K, Iwata T, Terasaki H.

Retina. 2018 Oct 9. doi: 10.1097/IAE.0000000000002363. [Epub ahead of print]

PMID:
30308565
18.

Clinical Features of Japanese Patients With Anti-╬▒-enolase Antibody-Positive Autoimmune Retinopathy: Novel Subtype of Multiple Drusen.

Ando R, Saito W, Kanda A, Kase S, Fujinami K, Sugahara M, Nakamura Y, Eguchi S, Mori S, Noda K, Shinoda K, Ishida S.

Am J Ophthalmol. 2018 Dec;196:181-196. doi: 10.1016/j.ajo.2018.08.044. Epub 2018 Sep 7.

PMID:
30195891
19.

A Cross-Sectional and Longitudinal Study of Retinal Sensitivity in RPE65-Associated Leber Congenital Amaurosis.

Kumaran N, Rubin GS, Kalitzeos A, Fujinami K, Bainbridge JWB, Weleber RG, Michaelides M.

Invest Ophthalmol Vis Sci. 2018 Jul 2;59(8):3330-3339. doi: 10.1167/iovs.18-23873. Erratum in: Invest Ophthalmol Vis Sci. 2018 Aug;59(10):4326.

20.

VALIDITY AND EFFICACY OF INTERNAL LIMITING MEMBRANE PEELING DURING INITIAL VITRECTOMY FOR RHEGMATOGENOUS RETINAL DETACHMENT: VISUAL OUTCOMES IN MACULA-SPARING CASES.

Akiyama K, Fujinami K, Watanabe K, Fukui M, Tsunoda K, Noda T.

Retin Cases Brief Rep. 2018 Jun 25. doi: 10.1097/ICB.0000000000000758. [Epub ahead of print]

PMID:
29944610
21.

ISCEV extended protocol for the dark-adapted red flash ERG.

Thompson DA, Fujinami K, Perlman I, Hamilton R, Robson AG.

Doc Ophthalmol. 2018 Jun;136(3):191-197. doi: 10.1007/s10633-018-9644-z. Epub 2018 Jun 22.

22.

Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.

Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, Wojciechowski R, Zrenner E, Michaelides M, Scholl HPN; ProgStar Study Group; ProgStar Study Group.

Br J Ophthalmol. 2019 Mar;103(3):390-397. doi: 10.1136/bjophthalmol-2018-312064. Epub 2018 Jun 20.

23.

Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10.

Kong X, Fujinami K, Strauss RW, Munoz B, West SK, Cideciyan AV, Michaelides M, Ahmed M, Ervin AM, Sch├Ânbach E, Cheetham JK, Scholl HPN; ProgStar Study Group.

JAMA Ophthalmol. 2018 Aug 1;136(8):920-928. doi: 10.1001/jamaophthalmol.2018.2198.

24.

Macular dysfunction in patients with macula-on rhegmatogenous retinal detachments.

Akiyama K, Fujinami K, Watanabe K, Noda T, Miyake Y, Tsunoda K.

Br J Ophthalmol. 2019 Mar;103(3):404-409. doi: 10.1136/bjophthalmol-2018-312153. Epub 2018 Jun 1.

PMID:
29858185
25.

Retinal findings in a patient with mutations in ABCC6 and ABCA4.

Mahroo OA, Fujinami K, Moore AT, Webster AR.

Eye (Lond). 2018 Sep;32(9):1542-1543. doi: 10.1038/s41433-018-0106-3. Epub 2018 May 16. No abstract available.

26.

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.

Khan KN, Kasilian M, Mahroo OAR, Tanna P, Kalitzeos A, Robson AG, Tsunoda K, Iwata T, Moore AT, Fujinami K, Michaelides M.

Ophthalmology. 2018 May;125(5):735-746. doi: 10.1016/j.ophtha.2017.11.020. Epub 2018 Jan 6.

27.

Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variants.

Kominami A, Ueno S, Kominami T, Nakanishi A, Ito Y, Fujinami K, Tsunoda K, Hayashi T, Kikuchi S, Kameya S, Iwata T, Terasaki H.

Ophthalmic Genet. 2018 Apr;39(2):255-262. doi: 10.1080/13816810.2017.1408846. Epub 2017 Dec 8.

PMID:
29220607
28.

Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular Dystrophy.

Kato Y, Hanazono G, Fujinami K, Hatase T, Kawamura Y, Iwata T, Miyake Y, Tsunoda K.

Invest Ophthalmol Vis Sci. 2017 Dec 1;58(14):6020-6029. doi: 10.1167/iovs.17-21969.

PMID:
29196766
29.

Advanced quantitative analysis of the sub-retinal pigment epithelial space in recurrent neovascular age-related macular degeneration.

Sasaki M, Kato Y, Fujinami K, Hirakata T, Tsunoda K, Watanabe K, Akiyama K, Noda T.

PLoS One. 2017 Nov 2;12(11):e0186955. doi: 10.1371/journal.pone.0186955. eCollection 2017.

30.

Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females.

Fiorentino A, Fujinami K, Arno G, Robson AG, Pontikos N, Arasanz Armengol M, Plagnol V, Hayashi T, Iwata T, Parker M, Fowler T, Rendon A, Gardner JC, Henderson RH, Cheetham ME, Webster AR, Michaelides M, Hardcastle AJ; 100,000 Genomes Project, the Japan Eye Genetic Consortium and the UK Inherited Retinal Dystrophy Consortium.

Hum Mutat. 2018 Jan;39(1):80-91. doi: 10.1002/humu.23349. Epub 2017 Oct 17.

PMID:
28967191
31.

The Effects of Different Doses and Patterns of Docetaxel Chemotherapy in Japanese Patients with Castration-Resistant Prostate Cancer.

Tatenuma T, Kawahara T, Miyoshi Y, Fujinami K, Ohta J, Kobayashi K, Kishida T, Yao M, Uemura H.

Curr Urol. 2017 Aug;10(3):166-168. doi: 10.1159/000447175. Epub 2017 Jul 30. No abstract available.

32.

Electro-optic probe measurements of electric fields in plasmas.

Nishiura M, Yoshida Z, Mushiake T, Kawazura Y, Osawa R, Fujinami K, Yano Y, Saitoh H, Yamasaki M, Kashyap A, Takahashi N, Nakatsuka M, Fukuyama A.

Rev Sci Instrum. 2017 Feb;88(2):023501. doi: 10.1063/1.4974740.

PMID:
28249485
33.

The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous Patients.

Fakin A, Robson AG, Chiang JP, Fujinami K, Moore AT, Michaelides M, Holder GE, Webster AR.

Invest Ophthalmol Vis Sci. 2016 Nov 1;57(14):5963-5973. doi: 10.1167/iovs.16-20446.

PMID:
27820952
34.

Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.

Tanna P, Strauss RW, Fujinami K, Michaelides M.

Br J Ophthalmol. 2017 Jan;101(1):25-30. doi: 10.1136/bjophthalmol-2016-308823. Epub 2016 Aug 4. Review.

35.

Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy.

Fujinami K, Kameya S, Kikuchi S, Ueno S, Kondo M, Hayashi T, Shinoda K, Machida S, Kuniyoshi K, Kawamura Y, Akahori M, Yoshitake K, Katagiri S, Nakanishi A, Sakuramoto H, Ozawa Y, Tsubota K, Yamaki K, Mizota A, Terasaki H, Miyake Y, Iwata T, Tsunoda K.

Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4837-46. doi: 10.1167/iovs.16-19670.

PMID:
27623337
36.

Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4.

Fakin A, Robson AG, Fujinami K, Moore AT, Michaelides M, Pei-Wen Chiang J, E Holder G, Webster AR.

Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4668-78. doi: 10.1167/iovs.16-19829.

PMID:
27583828
37.

Internal Limiting Membrane Peeling to Prevent Post-vitrectomy Epiretinal Membrane Development in Retinal Detachment.

Akiyama K, Fujinami K, Watanabe K, Tsunoda K, Noda T.

Am J Ophthalmol. 2016 Nov;171:1-10. doi: 10.1016/j.ajo.2016.08.015. Epub 2016 Aug 18.

PMID:
27544480
38.

Evaluation of cone function by a handheld non-mydriatic flicker electroretinogram device.

Nakamura N, Fujinami K, Mizuno Y, Noda T, Tsunoda K.

Clin Ophthalmol. 2016 Jun 30;10:1175-85. doi: 10.2147/OPTH.S104721. eCollection 2016.

39.

One-year outcome of intravitreal aflibercept injection for age-related macular degeneration resistant to ranibizumab: rapid morphologic recovery and subsequent visual improvement.

Hirakata T, Fujinami K, Watanabe K, Sasaki M, Noda T, Akiyama K.

Clin Ophthalmol. 2016 May 26;10:969-77. doi: 10.2147/OPTH.S101596. eCollection 2016.

40.

Neuroprotective effect of activated 5'-adenosine monophosphate-activated protein kinase on cone system function during retinal inflammation.

Kamoshita M, Fujinami K, Toda E, Tsubota K, Ozawa Y.

BMC Neurosci. 2016 Jun 10;17(1):32. doi: 10.1186/s12868-016-0268-5.

41.

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy in Japanese Cohort.

Nakanishi A, Ueno S, Hayashi T, Katagiri S, Kominami T, Ito Y, Gekka T, Masuda Y, Tsuneoka H, Shinoda K, Hirakata A, Inoue M, Fujinami K, Tsunoda K, Iwata T, Terasaki H.

Am J Ophthalmol. 2016 Aug;168:86-94. doi: 10.1016/j.ajo.2016.04.023. Epub 2016 May 7.

PMID:
27163236
42.

Recombinant Fusion Allergens, Cry j 1 and Cry j 2 from Japanese Cedar Pollen, Conjugated with Polyethylene Glycol Potentiate the Attenuation of Cry j 1-Specific IgE Production in Cry j 1-Sensitized Mice and Japanese Cedar Pollen Allergen-Sensitized Monkeys.

Fujimura T, Fujinami K, Ishikawa R, Tateno M, Tahara Y, Okumura Y, Ohta H, Miyazaki H, Taniguchi M.

Int Arch Allergy Immunol. 2015;168(1):32-43. doi: 10.1159/000441141. Epub 2015 Nov 3.

43.

Macular Hole Associated with Vogt-Koyanagi-Harada Disease at the Acute Uveitic Stage.

Mizuno M, Fujinami K, Watanabe K, Akiyama K.

Case Rep Ophthalmol. 2015 Sep 15;6(3):328-32. doi: 10.1159/000440679. eCollection 2015 Sep-Dec.

44.

Nomogram for overall survival of Japanese patients with bone-metastatic prostate cancer.

Miyoshi Y, Noguchi K, Yanagisawa M, Taguri M, Morita S, Ikeda I, Fujinami K, Miura T, Kobayashi K, Uemura H.

BMC Cancer. 2015 May 1;15:338. doi: 10.1186/s12885-015-1330-x.

45.

Association of Retinal Artery and Other Inner Retinal Structures With Distribution of Tapetal-like Reflex in Oguchi's Disease.

Kato Y, Tsunoda K, Fujinami K, Iwata T, Saga M, Oguchi Y.

Invest Ophthalmol Vis Sci. 2015 Apr;56(4):2162-72. doi: 10.1167/iovs.14-16198.

PMID:
25744976
46.

Androgen deprivation therapy prevents bladder cancer recurrence.

Izumi K, Taguri M, Miyamoto H, Hara Y, Kishida T, Chiba K, Murai T, Hirai K, Suzuki K, Fujinami K, Ueki T, Udagawa K, Kitami K, Moriyama M, Miyoshi Y, Tsuchiya F, Ikeda I, Kobayashi K, Sato M, Morita S, Noguchi K, Uemura H.

Oncotarget. 2014 Dec 30;5(24):12665-74.

47.

Clinical course of focal choroidal excavation in Vogt-Koyanagi-Harada disease.

Nishikawa Y, Fujinami K, Watanabe K, Noda T, Tsunoda K, Akiyama K.

Clin Ophthalmol. 2014 Dec 4;8:2461-5. doi: 10.2147/OPTH.S75558. eCollection 2014.

48.

Branch retinal artery occlusion secondary to prepapillary arterial loop.

Singh R, Fujinami K, Moore AT.

Retin Cases Brief Rep. 2014 Spring;8(2):124-6. doi: 10.1097/ICB.0000000000000020.

PMID:
25372326
49.

Clinical and molecular characteristics of childhood-onset Stargardt disease.

Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT.

Ophthalmology. 2015 Feb;122(2):326-34. doi: 10.1016/j.ophtha.2014.08.012. Epub 2014 Oct 12.

50.

Haptic breakage after transscleral fixation of a single-piece acrylic intraocular lens.

Tanaka H, Fujinami K, Watanabe K, Noda T, Akiyama K.

Case Rep Ophthalmol. 2014 Jul 12;5(2):212-6. doi: 10.1159/000365350. eCollection 2014 May.

Supplemental Content

Loading ...
Support Center