Kaoru Fujinami

发表

KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2

E. Zrenner, D. Sharon, K. Tsunoda, 2021, American journal of ophthalmology.

Spatial Functional Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake disease); EAOMD Report No.2.

K. Tsubota, K. Tsunoda, Nikolas Pontikos, 2020, American journal of ophthalmology.

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

K. Tsubota, K. Tsunoda, G. Arno, 2019, Ophthalmology.

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

K. Tsunoda, N. Pontikos, K. Yoshitake, 2019, Journal of ophthalmology.

Fundus autofluorescence in autosomal dominant occult macular dystrophy.

K. Tsunoda, Y. Miyake, Kaoru Fujinami, 2011, Archives of ophthalmology.

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

K. Tsunoda, K. Yoshitake, Kaoru Fujinami, 2019, Documenta Ophthalmologica.

Longitudinal Changes of Fixation Stability and Location within 24 Months in Stargardt Disease: ProgStar Report No. 16: Short title: Longitudinal Changes of Fixation in Stargardt Disease.

A. Cideciyan, E. Zrenner, M. Cattaneo, 2021, American journal of ophthalmology.

Progress of macular atrophy during 30 months’ follow-up in a patient with spinocerebellar ataxia type1 (SCA1)

K. Tsunoda, T. Matsuura, Kaoru Fujinami, 2020, Documenta Ophthalmologica.

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

K. Tsunoda, Kaoru Fujinami, Ken Watanabe, 2016, American journal of ophthalmology.

ISCEV extended protocol for the dark-adapted red flash ERG

Dorothy A. Thompson, I. Perlman, R. Hamilton, 2018, Documenta ophthalmologica. Advances in ophthalmology.

Stargardt Macular Dystrophy

Nikolas Pontikos, G. Arno, Kaoru Fujinami, 2022, Inherited Retinal Disease.

Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1

K. Tsubota, K. Tsunoda, Kaoru Fujinami, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

K. Tsubota, G. Holder, K. Tsunoda, 2014, Ophthalmology.

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

J. Sahel, A. Cideciyan, E. Zrenner, 2018, British Journal of Ophthalmology.

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

M. Michaelides, R. Strauss, M. Georgiou, 2019, Translational vision science & technology.

Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency

Y. Hayashizaki, M. Itoh, H. Kawaji, 2020, Scientific Reports.

Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches

M. Michaelides, A. Moore, M. Georgiou, 2020, British Journal of Ophthalmology.

Ocular findings in Japanese patients with hydroxychloroquine retinopathy developing within 3 years of treatment

D. Browning, M. Kondo, Seong Joon Ahn, 2021, Japanese Journal of Ophthalmology.

Fish oil supplementation and repeated macular hemorrhage without choroidal neovascularization: A case report

S. Crewther, Kaoru Fujinami, Z. Yin, 2020, SAGE open medical case reports.

The Progression of Stargardt Disease using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15.

A. Cideciyan, S. Sadda, J. Sunness, 2021, American journal of ophthalmology.

Stargardt Macular Dystrophy

Nikolas Pontikos, G. Arno, Kaoru Fujinami, 2022, Inherited Retinal Disease.

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

G. Holder, M. Michaelides, A. Webster, 2016, Investigative ophthalmology & visual science.

Retina The Effect on Retinal Structure and Function of 15 Specific ABCA 4 Mutations : A Detailed Examination of 82 Hemizygous Patients

G. Holder, M. Michaelides, A. Webster, 2016 .

Stargardt Disease in Asian Population

G. Arno, Kaoru Fujinami, Xiao Liu, 2018, Essentials in Ophthalmology.

Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D-Associated Retinal Disorder

K. Tsubota, K. Tsunoda, Nikolas Pontikos, 2020, Translational vision science & technology.

Longitudinal follow‐up of siblings with a discordant Stargardt disease phenotype

M. Michaelides, A. Moore, Kaoru Fujinami, 2014, Acta ophthalmologica.

Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History

M. Michaelides, A. Webster, M. Georgiou, 2020, American journal of ophthalmology.

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

V. Plagnol, Nikolas Pontikos, G. Arno, 2018, Human mutation.

Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up

Kaoru Fujinami, Xiao Liu, Lixia Gao, 2020, Documenta Ophthalmologica.

New variants and in silico analyses in GRK1 associated Oguchi disease

Rachel L. Taylor, C. Rivolta, D. Donnelly, 2020, Human mutation.

New pathogenic variants and insights into pathogenic mechanisms in GRK1-related Oguchi disease

Rachel L. Taylor, C. Rivolta, D. Donnelly, 2020, bioRxiv.

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

K. Tsunoda, Kaoru Fujinami, T. Iwata, 2015, Investigative ophthalmology & visual science.

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

A. Cideciyan, B. Munoz, S. West, 2018, JAMA ophthalmology.

Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association

Y. Hayashizaki, H. Kawaji, K. Tsubota, 2020, Scientific Reports.

Fine central macular dots associated with childhood‐onset Stargardt Disease

M. Michaelides, A. Moore, R. Allikmets, 2014, Acta ophthalmologica.

Clinical and genetic characteristics of 10 Japanese patients with PROM1‐associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population

K. Tsubota, K. Tsunoda, A. Tsujikawa, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients.

K. Tsunoda, Y. Momozawa, A. Tsujikawa, 2021, Ophthalmology. Retina.

Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy

K. Tsunoda, T. Tachibana, K. Yoshitake, 2020, International journal of molecular sciences.

X-linked Retinoschisis: Deep Phenotyping and Genetic Characterization.

G. Virgili, O. Mahroo, M. Michaelides, 2021, Ophthalmology.

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

K. Tsubota, Y. Ozawa, Kaoru Fujinami, 2016, BMC Neuroscience.

RETINAL SURFACE WRINKLING AS AN INDICATOR FOR INTERNAL LIMITING MEMBRANE PEELING DURING VITRECTOMY FOR RETINAL DETACHMENT

K. Tsunoda, Kaoru Fujinami, T. Matsuki, 2020, Retina.

Haptic Breakage after Transscleral Fixation of a Single-Piece Acrylic Intraocular Lens

Kaoru Fujinami, Ken Watanabe, K. Akiyama, 2014, Case Reports in Ophthalmology.

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

K. Tsunoda, Y. Masuda, Kaoru Fujinami, 2016, American journal of ophthalmology.

Three cases of acute-onset bilateral photophobia

K. Tsunoda, Kaoru Fujinami, T. Iwata, 2019, Japanese Journal of Ophthalmology.

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing

K. Tsunoda, Makoto Nakamura, K. Yoshitake, 2022, Human mutation.

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

K. Tsunoda, Kaoru Fujinami, Ken Watanabe, 2018, Retinal cases & brief reports.

Case of acute zonal occult outer retinopathy with abnormal pattern visual evoked potentials

K. Tsunoda, Kaoru Fujinami, H. Yamazaki, 2011, Clinical ophthalmology.

Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques

K. Tsunoda, N. Pontikos, K. Yoshitake, 2021, British Journal of Ophthalmology.

Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review

Pádraig J. Mulholland, S. Tuft, K. Balaskas, 2021, JMIR medical informatics.

Choroidal neovascularization in a child following laser pointer-induced macular injury

Kaoru Fujinami, T. Yokoi, S. Nishina, 2010, Japanese Journal of Ophthalmology.

Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in NMNAT1: a case report and mini review

K. Tsunoda, K. Yoshitake, Kaoru Fujinami, 2022, Ophthalmic genetics.

RP2‐associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype–phenotype association

K. Tsubota, K. Tsunoda, Nikolas Pontikos, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Inherited retinal diseases: Therapeutics, clinical trials and end points—A review

M. Michaelides, M. Georgiou, Kaoru Fujinami, 2021, Clinical & experimental ophthalmology.

Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association

Y. Hayashizaki, H. Kawaji, K. Tsubota, 2020, Scientific Reports.

Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings

K. Tsunoda, T. Tachibana, K. Yoshitake, 2020, Molecular genetics & genomic medicine.

Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3

K. Tsunoda, M. Kondo, Seong Joon Ahn, 2022, Investigative ophthalmology & visual science.

Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene.

K. Tsunoda, Makoto Nakamura, Y. Miyake, 2011, Archives of ophthalmology.

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

Takeshi Iwata, Satoshi Katagiri, Kimitaka Kaga, 2019, Molecular vision.

Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan

K. Tsunoda, A. Tsujikawa, Makoto Nakamura, 2021, Genes.

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

T. Morimoto, K. Tsunoda, K. Yoshitake, 2019, Human Genome Variation.

Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy

K. Tsunoda, O. Mahroo, M. Michaelides, 2018, Ophthalmology.

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

K. Tsunoda, Kaoru Fujinami, Takaaki Hayashi, 2018, Ophthalmic genetics.

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

K. Tsubota, K. Tsunoda, Y. Ozawa, 2016, Investigative ophthalmology & visual science.

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

Michel Michaelides, M. Michaelides, R. Strauss, 2016, British Journal of Ophthalmology.

Molecular characteristics of four Japanese cases with KCNV2 retinopathy: Report of novel disease-causing variants

K. Tsubota, K. Tsunoda, Y. Ozawa, 2013, Molecular vision.

A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.

K. Tsubota, E. Stone, G. Holder, 2013, American journal of ophthalmology.

The clinical effect of homozygous ABCA4 alleles in 18 patients.

K. Tsubota, G. Holder, K. Tsunoda, 2013, Ophthalmology.

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.

K. Tsubota, G. Holder, K. Tsunoda, 2013, American journal of ophthalmology.

Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics

A. Hoischen, C. Klaver, D. Sharon, 2019, bioRxiv.

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

K. Tsunoda, Nikolas Pontikos, G. Arno, 2019, Investigative ophthalmology & visual science.

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

M. Michaelides, A. Webster, A. Moore, 2016, Investigative ophthalmology & visual science.

Retina Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA 4

G. Holder, M. Michaelides, A. Webster, 2016 .

CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History

O. Mahroo, M. Michaelides, A. Webster, 2022, American journal of ophthalmology.

Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease Symmetry

M. Michaelides, R. Strauss, M. Georgiou, 2019, American journal of ophthalmology.

Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11.

J. Sahel, A. Cideciyan, E. Zrenner, 2019, JAMA ophthalmology.

A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.

K. Tsubota, E. Stone, K. Tsunoda, 2013, Investigative ophthalmology & visual science.

ABCA4 gene screening by next-generation sequencing in a British cohort.

K. Tsubota, K. Tsunoda, M. Michaelides, 2013, Investigative ophthalmology & visual science.

Stargardt Disease with Preserved Central Vision: identification of a putative novel mutation in ATP‐binding cassette transporter gene

K. Tsunoda, Y. Miyake, Kaoru Fujinami, 2011, Acta ophthalmologica.

Multisystem Inflammatory Syndrome in Adults after Mild SARS-CoV-2 Infection, Japan

T. Eguchi, Kaoru Fujinami, N. Mori, 2021, Emerging infectious diseases.

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

K. Tsunoda, K. Yoshitake, M. Kondo, 2019, Investigative ophthalmology & visual science.

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

K. Tsunoda, T. Hatase, Y. Miyake, 2017, Investigative ophthalmology & visual science.

Retina Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP 1 L 1 Mutations in Families With Occult Macular Dystrophy

K. Tsunoda, T. Hatase, Y. Miyake, 2017 .

CLINICAL CHARACTERISTICS OF OCCULT MACULAR DYSTROPHY IN FAMILY WITH MUTATION OF RP1L1 GENE

K. Tsunoda, T. Hatase, Y. Miyake, 2012, Retina.

Selective abnormality of cone outer segment tip line in acute zonal occult outer retinopathy as observed by spectral-domain optical coherence tomography.

K. Tsunoda, Y. Miyake, Kaoru Fujinami, 2011, Archives of ophthalmology.

Transient macular dysfunction determined by focal macular electroretinogram

K. Tsunoda, Y. Miyake, Kaoru Fujinami, 2007, British Journal of Ophthalmology.

Macular dysfunction in patients with macula-on rhegmatogenous retinal detachments

K. Tsunoda, Y. Miyake, Kaoru Fujinami, 2018, British Journal of Ophthalmology.

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

Kaoru Fujinami, Ken Watanabe, K. Akiyama, 2015, Case Reports in Ophthalmology.

[Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram].

K. Tsunoda, T. Hatase, Y. Miyake, 2013, Nippon Ganka Gakkai zasshi.

K. Tsunoda, T. Matsuura, K. Yoshitake, 2020, Investigative ophthalmology & visual science.

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

K. Tsunoda, K. Yamaki, Kaoru Fujinami, 2019, Ophthalmic surgery, lasers & imaging retina.

Retinal imaging in inherited retinal diseases

M. Michaelides, M. Georgiou, Kaoru Fujinami, 2020, Annals of eye science.

CHANGES OF CONE PHOTORECEPTOR MOSAIC IN AUTOSOMAL RECESSIVE BESTROPHINOPATHY.

K. Tsunoda, Kaoru Fujinami, Takaaki Hayashi, 2018, Retina.

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

K. Tsunoda, K. Yoshitake, Y. Miyake, 2019, Human Genome Variation.

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

K. Tsunoda, K. Yoshitake, Y. Miyake, 2019, Human Genome Variation.

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

K. Tsunoda, Kaoru Fujinami, Natsuko Nakamura, 2016, Clinical ophthalmology.

Acute unilateral inner retinal dysfunction with photophobia: importance of electrodiagnosis

K. Tsunoda, A. Murakami, A. Kanda, 2020, Japanese Journal of Ophthalmology.

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

K. Tsubota, Y. Ozawa, Kaoru Fujinami, 2016, BMC Neuroscience.

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

K. Tsunoda, T. Matsuura, K. Yoshitake, 2019, Scientific Reports.

Clinical course of focal choroidal excavation in Vogt–Koyanagi–Harada disease

K. Tsunoda, Kaoru Fujinami, Ken Watanabe, 2014, Clinical ophthalmology.

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

K. Tsunoda, Kaoru Fujinami, M. Sasaki, 2017, PloS one.

A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case report

K. Tsunoda, S. Saitoh, M. Kondo, 2022, Medicine.

A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family

Nikolas Pontikos, M. Michaelides, K. Mochizuki, 2022, Ophthalmic genetics.

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

G. Rubin, M. Michaelides, J. Bainbridge, 2018, Investigative ophthalmology & visual science.

Challenges and Opportunities in the Genetic Analysis of Inherited Retinal Dystrophies in Africa, a Literature Review

W. Jaoko, Kaoru Fujinami, M. Mureithi, 2023, Journal of personalized medicine.

Long-term follow-up of a Chinese patient with KCNV2-retinopathy

K. Tsubota, Kaoru Fujinami, Yu Fujinami-Yokokawa, 2020, Ophthalmic genetics.

KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course—KCNV2 Study Group Report 1

E. Zrenner, D. Sharon, K. Tsunoda, 2020, American journal of ophthalmology.

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

Nikolas Pontikos, G. Arno, M. Michaelides, 2019, American journal of ophthalmology.

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

K. Tsunoda, K. Yoshitake, Kaoru Fujinami, 2018, American journal of ophthalmology case reports.

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

Kaoru Fujinami, M. Sasaki, Ken Watanabe, 2016, Clinical ophthalmology.

A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder

K. Tsunoda, K. Yamazawa, H. Ohashi, 2021, Human genome variation.

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

S. Kase, A. Kanda, K. Noda, 2018, American journal of ophthalmology.

Fundus autofluorescence imaging in a patient with the juvenile form of galactosialidosis.

K. Tsubota, K. Tsunoda, Kaoru Fujinami, 2014, Ophthalmic surgery, lasers & imaging retina.

Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia

K. Tsunoda, Kaoru Fujinami, Takaaki Hayashi, 2023, Genes.

CERKL-associated retinal dystrophy: Genetics, Phenotype and Natural History.

O. Mahroo, M. Michaelides, A. Webster, 2023, Ophthalmology. Retina.

Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)

K. Balaskas, O. Mahroo, Nikolas Pontikos, 2023, BMJ Open.

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

A. Hoischen, C. Klaver, D. Sharon, 2020, Genetics in Medicine.

Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review

Pádraig J. Mulholland, S. Tuft, K. Balaskas, 2021, JMIR medical informatics.

ABCA4 gene screening by next-generation sequencing in a British cohort.

K. Tsubota, K. Tsunoda, M. Michaelides, 2013, Investigative ophthalmology & visual science.

Stargardt macular dystrophy and therapeutic approaches

Kaoru Fujinami, Yu Fujinami-Yokokawa, Paul Yang, 2023, The British journal of ophthalmology.

Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No. 5

K. Tsunoda, M. Kondo, Seong Joon Ahn, 2023, Genes.

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

K. Tsunoda, T. Hatase, Y. Miyake, 2017, Investigative ophthalmology & visual science.

Case of acute zonal occult outer retinopathy with abnormal pattern visual evoked potentials

K. Tsunoda, Kaoru Fujinami, H. Yamazaki, 2011 .