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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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Pedicle Internal Limiting Membrane Transposition Flap Technique for Refractory Macular Hole

Ophthalmic surgery, lasers & imaging retina, 2015-11, Vol.46 (10), p.1045-1046

2015

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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.187-190

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.38-43

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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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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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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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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High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation

Ophthalmic surgery, lasers & imaging retina, 2016-12, Vol.47 (12), p.1115-1126

2016

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Improved Photoreceptor Function in Male Acute Zonal Occult Outer Retinopathy

Optometry and vision science, 2015-10, Vol.92 (10), p.e371-e379

2015

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OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina

Documenta ophthalmologica, 2014-04, Vol.128 (2), p.137-148

2014

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Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia

Ophthalmic genetics, 2016, Vol.37 (1), p.68-75

2016

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Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia

Visual neuroscience, 2006-05, Vol.23 (3-4), p.395-402

2006

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Compound heterozygous RDH5 mutations in familial fleck retina with night blindness

Acta ophthalmologica Scandinavica, 2006-04, Vol.84 (2), p.254-258

2006

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Enhanced S‐cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X)

Acta ophthalmologica Scandinavica, 2004-10, Vol.82 (5), p.616-622

2004

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Long-Term Course Following Vitreous Surgery for Epiretinal Membrane

Clinical and genetic findings of autosomal recessive bestrophinopathy in Japanese cohort

Pedicle Internal Limiting Membrane Transposition Flap Technique for Refractory Macular Hole

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

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

Multimodal imaging of a case of peripheral cone dystrophy

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

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

High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation

Improved Photoreceptor Function in Male Acute Zonal Occult Outer Retinopathy

OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina

Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia

Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia

Compound heterozygous RDH5 mutations in familial fleck retina with night blindness

Enhanced S‐cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X)

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