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Long-Term Course Following Vitreous Surgery for Epiretinal Membrane

Ophthalmic surgery, lasers & imaging retina, 2019-04, Vol.50 (4), p.e105

2019

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Clinical and genetic findings of autosomal recessive bestrophinopathy in Japanese cohort

American journal of ophthalmology, 2016-08, Vol.168, p.86-94

2016

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Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses

Documenta ophthalmologica, 2019-06, Vol.138 (3), p.229-239

2019

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Pedicle Internal Limiting Membrane Transposition Flap Technique for Refractory Macular Hole

Ophthalmic surgery, lasers & imaging retina, 2015-11, Vol.46 (10), p.1045

2015

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Analysis of Changes in Corneal Topography after 27-Gauge Transconjunctival Microincision Vitrectomy Combined with Cataract Surgery

Journal of ophthalmology, 2019, Vol.2019, p.9658204-5

2019

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Subfoveal choroidal thickness in multiple evanescent white dot syndrome

Clinical and experimental optometry, 2012-03, Vol.95 (2), p.212-217

2012

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Spontaneous Resolution of Large Macular Retinoschisis in Enhanced S-Cone Syndrome

Ophthalmic surgery, lasers & imaging retina, 2016-02, Vol.47 (2), p.187

2016

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Early postoperative evaluation of retinal function by electroretinography after vitreous surgery for idiopathic epimacular membrane

Documenta ophthalmologica, 2017-06, Vol.134 (3), p.167-173

2017

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Efficacy of Intravitreal Triamcinolone Acetonide for Diabetic Macular Edema After Vitrectomy

Journal of ocular pharmacology and therapeutics, 2016-01, Vol.32 (1), p.38

2016

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Closure of a full-thickness macular hole without vitrectomy in choroideraemia

Clinical and experimental optometry, 2017-05, Vol.100 (3), p.294-295

2017

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Treatment of a dislocated lens by transcorneal vitrectomy and bimanual phacoemulsification

Clinical ophthalmology (Auckland, N.Z.), 2014-01, Vol.8 (default), p.1539-1542

2014

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Treatment of Dropped Nucleus with a 27-Gauge Twin Duty Cycle Vitreous Cutter

Case reports in ophthalmology, 2016-01, Vol.7 (1), p.44-48

2016

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Trisection technique for the extraction of dislocated intraocular lenses through a small surgical incision

Journal of cataract and refractive surgery, 2015-10, Vol.41 (10), p.2040-2042

2015

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Multimodal imaging of a case of peripheral cone dystrophy

Documenta ophthalmologica, 2015-06, Vol.130 (3), p.241-251

2015

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Improvement of central visual function following steroid pulse therapy in acute zonal occult outer retinopathy

Documenta ophthalmologica, 2012-06, Vol.124 (3), p.249-254

2012

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A Novel Homozygous GRK1 Mutation (P391H) in 2 Siblings with Oguchi Disease with Markedly Reduced Cone Responses

Ophthalmology (Rochester, Minn.), 2007, Vol.114 (1), p.134-141.e1

2007

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CYP4V2 Mutations in Two Japanese Patients with Bietti’s Crystalline Dystrophy

Ophthalmic research, 2005-09, Vol.37 (5), p.262-269

2005

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RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort

Investigative ophthalmology & visual science, 2020-03, Vol.61 (3), p.53-53

2020

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Mutation analysis of BEST1 in Japanese patients with Best's vitelliform macular dystrophy

British journal of ophthalmology, 2015-11, Vol.99 (11), p.1577-1582

2015

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A case of traction retinal detachment in a patient with Gaucher disease

Ophthalmic genetics, 2017-05, Vol.38 (3), p.273-276

2017

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Autosomal recessive cone–rod dystrophy associated with compound heterozygous mutations in the EYS gene

Documenta ophthalmologica, 2014-06, Vol.128 (3), p.211-217

2014

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Dominant Optic Atrophy Caused by a Novel OPA1 Splice Site Mutation (IVS20+1G→A) Associated with Intron Retention

Ophthalmic research, 2005-07, Vol.37 (4), p.214-224

2005

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Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect

Visual neuroscience, 2006-05, Vol.23 (3-4), p.411-417

2006

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A novel homozygous CYP4V2 variant (p.S121Y) associated with a choroideremia-like phenotype

Ophthalmic genetics, 2017-05, Vol.38 (3), p.286-287

2017

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Autosomal dominant occult macular dystrophy with an RP1L1 mutation (R45W)

Optometry and vision science, 2012-05, Vol.89 (5), p.684

2012

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Long-Term Course Following Vitreous Surgery for Epiretinal Membrane

Clinical and genetic findings of autosomal recessive bestrophinopathy in Japanese cohort

Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses

Pedicle Internal Limiting Membrane Transposition Flap Technique for Refractory Macular Hole

Analysis of Changes in Corneal Topography after 27-Gauge Transconjunctival Microincision Vitrectomy Combined with Cataract Surgery

Subfoveal choroidal thickness in multiple evanescent white dot syndrome

Spontaneous Resolution of Large Macular Retinoschisis in Enhanced S-Cone Syndrome

Early postoperative evaluation of retinal function by electroretinography after vitreous surgery for idiopathic epimacular membrane

Efficacy of Intravitreal Triamcinolone Acetonide for Diabetic Macular Edema After Vitrectomy

Closure of a full-thickness macular hole without vitrectomy in choroideraemia

Treatment of a dislocated lens by transcorneal vitrectomy and bimanual phacoemulsification

Treatment of Dropped Nucleus with a 27-Gauge Twin Duty Cycle Vitreous Cutter

Trisection technique for the extraction of dislocated intraocular lenses through a small surgical incision

Multimodal imaging of a case of peripheral cone dystrophy

Improvement of central visual function following steroid pulse therapy in acute zonal occult outer retinopathy

A Novel Homozygous GRK1 Mutation (P391H) in 2 Siblings with Oguchi Disease with Markedly Reduced Cone Responses

CYP4V2 Mutations in Two Japanese Patients with Bietti’s Crystalline Dystrophy

RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort

Mutation analysis of BEST1 in Japanese patients with Best's vitelliform macular dystrophy

A case of traction retinal detachment in a patient with Gaucher disease

Autosomal recessive cone–rod dystrophy associated with compound heterozygous mutations in the EYS gene

Dominant Optic Atrophy Caused by a Novel OPA1 Splice Site Mutation (IVS20+1G→A) Associated with Intron Retention

Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect

A novel homozygous CYP4V2 variant (p.S121Y) associated with a choroideremia-like phenotype

Autosomal dominant occult macular dystrophy with an RP1L1 mutation (R45W)

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