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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.1045-1046

2015

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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.187-190

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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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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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.684-691

2012

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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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Fundus autofluorescence findings of acute posterior multifocal placoid pigment epitheliopathy with chronic thyroiditis and splenectomy

Clinical and experimental optometry, 2015-03, Vol.98 (2), p.186-189

2015

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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

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

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

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)

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

Fundus autofluorescence findings of acute posterior multifocal placoid pigment epitheliopathy with chronic thyroiditis and splenectomy

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