Evaluation of inner retinal function at different stages of primary open angle glaucoma
using the photopic negative
response (PhNR) measured by RETeval electroretinography.
Hidaka T, Chuman H, Yasuhiro I
Graefes Arch Clin Exp Ophthalmol. 262(1): 161-169, 2024.
DOI: 10.1007/s00417-023-06193-z.
抗アクアポリン4抗体陽性視神経炎の視力の経過
山添早織、中馬秀樹、池田康博.
臨眼. 78: 823-827, 2024.
Comparison of Microperimetry and Static Perimetry for Evaluating Macular Function and
Progression in Retinitis
Pigmentosa.
Fukushima M, Tao Y, Shimokawa S, Zhao H, Shimokawa S, Funatsu J, Hisai T, Okita A, Fujiwara K, Hisatomi
T, Takeda A,
Ikeda Y, Sonoda KH, Murakami Y.
Ophthalmol Sci. 4: 100582, 2024. doi: 10.1016/j.xops.2024.100582. eCollection 2024 Nov-Dec.
Intraocular kinetics of pathological ATP after photoreceptor damage in rhegmatogenous
retinal detachment.
Tachibana T, Notomi S, Funatsu J, Fujiwara K, Nakatake S, Murakami Y, Nakao S, Kanamoto T, Ikeda Y,
Ishibashi T, Sonoda
KH, Hisatomi T.
Jpn J Ophthalmol. 68: 500-510, 2024.
Safety and efficacy of ripasudil eye drops in preterm infants with retinopathy of
prematurity: phase 1/2, open label,
single-arm trial.
Arima M, Inoue H, Misumi A, Tsukamoto S, Matsushita I, Araki S, Ohta M, Takahashi K, Imazato M, Goto T,
Aoki Y, Tagawa
K, Hirose M, Fujita Y, Yoshida N, Nakao S, Kondo H, Kusuhara K, Kimura K, Hasegawa S, Ikeda Y, Kodama Y,
Moritake H,
Ochiai M, Ohga S, Kishimoto J, Todaka K, Ieiri I, Sonoda KH.
Jpn J Ophthalmol. 68: 490-499, 2024.
Japan Glaucoma Society Omics Group; Genomic Research Committee of the Japanese
Ophthalmological Society. Genetic Risk
Stratification of Primary Open-Angle Glaucoma in Japanese Individuals.
Akiyama M, Tamiya G, Fujiwara K, Shiga Y, Yokoyama Y, Hashimoto K, Sato M, Sato K, Narita A, Hashimoto
S, Ueda E, Furuta
Y, Hata J, Miyake M, Ikeda HO, Suda K, Numa S, Mori Y, Morino K, Murakami Y, Shimokawa S, Nakamura S,
Yawata N, Fujisawa
K, Yamana S, Mori K, Ikeda Y, Miyata K, Mori K, Ogino K, Koyanagi Y, Kamatani Y; Biobank Japan Project;
Ninomiya T,
Sonoda KH, Nakazawa T.
Ophthalmology. 131: 1271-1280, 2024.
Specification of variant interpretation guidelines for inherited retinal dystrophy in
Japan.
Fujinami K, Nishiguchi KM, Oishi A, Akiyama M, Ikeda Y; Research Group on Rare, Intractable Diseases
(Ministry of
Health, Labour, Welfare of Japan).
Jpn J Ophthalmol. 68: 389-399, 2024.
Efficacy of a wearable night-vision aid in patients with concentric peripheral visual
field loss: a randomized,
crossover trial.
Mawatari G, Hiwatashi S, Motani T, Nagatomo S, Ando E, Kuwahata T, Ishizu M, Ikeda Y.
Jpn J Ophthalmol. 68: 321-326, 2024.
Genotypes and clinical features of RHO-associated retinitis pigmentosa in a Japanese
population.
Tsutsui S, Murakami Y, Fujiwara K, Koyanagi Y, Akiyama M, Takeda A, Ikeda Y, Sonoda KH.
Jpn J Ophthalmol. 68(1):1-11,2024
DOI: 10.1007/s10384-023-01036-0.
Genetic and Clinical Features of ABCA4-Associated Retinopathy in a Japanese Nationwide
Cohort.
Mizobuchi K, Hayashi T, Tanaka K, Kuniyoshi K, Murakami Y, Nakamura N, Torii K, Mizota A, Sakai D,
Maeda A, Kominami T,
Ueno S, Kusaka S, Nishiguchi KM, Ikeda Y, Kondo M, Tsunoda K, Hotta Y, Nakano T.
Am J Ophthalmol. 264:36-43,2024
DOI: 10.1016/j.ajo.2024.03.007.
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese
patients with retinitis
pigmentosa and allied diseases.
Goto K, Koyanagi Y, Akiyama M, Murakami Y, Fukushima M, Fujiwara K, Iijima H, Yamaguchi M, Endo M,
Hashimoto K, Ishizu
M, Hirakata T, Mizobuchi K, Takayama M, Ota J, Sajiki AF, Kominami T, Ushida H, Fujita K, Kaneko H, Ueno
S, Hayashi T,
Terao C, Hotta Y, Murakami A, Kuniyoshi K, Kusaka S, Wada Y, Abe T, Nakazawa T, Ikeda Y, Momozawa Y,
Sonoda KH,
Nishiguchi KM.
J Med Genet. jmg-2023-109750,2024
DOI: 10.1136/jmg-2023-109750
Evaluation of inner retinal function at different stages of primary open angle glaucoma
using the photopic negative
response (PhNR) measured by RETeval electroretinography
Hidaka T, Chuman H, Ikeda Y
Fraefes Arch Clin Exp Ophthalmol. 262(1):161-169,2024
DOI: 10.1007/s00417-023-06193-z
Proposed System for Selection of Surgical Approaches for Craniopharyngiomas Based on the
Optic Recess Displacement
Pattern.
Watanabe T, Uehara H, Takeishi G, Chuman H, Azuma M, Yokogami K, Takeshima H
World Neurosurg. 170: e817-e826, 2023.
DOI: 10.1016/j.wneu.2022.11.138.
Structure-function relationship between magnetic resonance imaging lesion areas and
visual field defects in initial
optic neuritis with altitudinal hemianopsia.
Ochi H, Kurimoto T, Yamagami A, Goto K, Miki A, Kawai M, Ishikawa H, Matsuzaki M, Kondo M, Mochizuki Y,
Kimura A,
Maekubo T, Chuman H, Ueki S, Nakamura M
Jpn J Ophthalmol. 67(5): 618-627, 2023.
DOI: 10.1007/s10384-023-01008-4.
Assessing the Correlation Between Visual Acuity and Critical Fusion Frequency in Acute
Optic Neuritis Before and After
Steroid Therapy.
Tsumura R, Harada Y, Chuman H, Kiuchi Y
Cureus. 15(12): e49965, 2023.
DOI: 10.7759/cureus.49965.
Structure-function relationship between magnetic resonance imaging lesion areas and
visual field defects in initial
optic neuritis with altitudinal hemianopsia.
Ochi H, Kurimoto T, Yamagami A, Goto K, Miki A, Kawai M, Ishikawa H, Matsuzaki M, Kondo M, Mochizuki Y,
Kimura A,
Maekubo T, Chuman H, Ueki S, Nakamura M.
Jpn J Ophthalmol. 67(5):618-627,2023
DOI: 10.1007/s10384-023-01008-4.
Assessing the Correlation Between Visual Acuity and Critical Fusion Frequency in Acute
Optic Neuritis Before and After
Steroid Therapy.
Tsumura R, Harada Y, Chuman H, Kiuchi Y.
Cureus. 15(12):e49965,2023
DOI: 10.7759/cureus.49965.
Proposed System for Selection of Surgical Approaches for Craniopharyngiomas Based on the
Optic Recess Displacement Pattern
Watanabe T, Uehara H, Takeishi G, Chuman H, Azuma M, Yokogami K, Takeshima H
World Neurosurg. 170:e817-e826,2023
DOI: 10.1016/j.wneu.2022.11.138
九州大学病院における緑内障手術の長期術後成績
木下博之、藤原康太、下川翔太郎、村上祐介、池田康博、園田康平.
眼臨紀. 15: 79-805, 2022.
Drinking hydrogen water improves photoreceptor structure and function in retinal
degeneration 6 mice.
Igarashi T, Ohsawa I, Kobayashi M, Miyazaki K, Igarashi T, Kameya S, Shiozawa AL, Ikeda Y, Miyagawa Y,
Sakai M, Okada T,
Sakane I, Takahashi H.
Sci Rep. 12: 13610, 2022.
Likely pathogenic structural variants in genetically unsolved patients with retinitis
pigmentosa revealed by long-read sequencing.
Sano Y, Koyanagi Y, Wong JH, Murakami Y, Fujiwara K, Endo M, Aoi T, Hashimoto K, Nakazawa T, Wada Y,
Ueno S, Gao D, Murakami A, Hotta Y, Ikeda Y, Nishiguchi KM, Momozawa Y, Sonoda KH, Akiyama M, Fujimoto
A.
J Med Genet. 59(11):1133-1138,2022
DOI: 10.1136/jmedgenet-2022-108428
Circulating inflammatory monocytes oppose microglia and contribute to cone cell death in
retinitis pigmentosa.
Funatsu J, Murakami Y, Shimokawa S, Nakatake S, Fujiwara K, Okita A, Fukushima M, Shibata K, Yoshida N,
Koyanagi Y, Akiyama M, Notomi S, Nakao S, Hisatomi T, Takeda A, Paschalis EI, Vavvas DG, Ikeda Y, Sonoda
KH
PNAS Nexus. 1(1):pgac003,2022
DOI: 10.1093/pnasnexus/pgac003
Long-term Outcomes of Cataract Surgery in Patients with Retinitis Pigmentosa.
Nakamura S, Fujiwara K, Yoshida N, Murakami Y, Shimokawa S, Koyanagi Y, Ikeda Y, Sonoda KH.
Ophthalmol Retina. 6(4):268-272,2022
DOI: 10.1016/j.oret.2021.12.010
Recurrence Rate of Cystoid Macular Edema with Topical Dorzolamide Treatment and Its Risk
Factors in Retinitis Pigmentosa.
Shimokawa S, Murakami Y, Fujiwara K, Funatsu J, Nakatake S, Koyanagi Y, Akiyama M, Yoshida N, Takeda A,
Ikeda Y, Sonoda KH
Retina. 42(1):168-173,2022
DOI: 10.1097/IAE.0000000000003286
A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1
gene
Lee J, Iwasaki T, Kaida T, Chuman H, Yoshimura A, Okamoto Y, Takashima H, Miyata K
Am J Ophthalmol Case Rep. 25:101-315,2022
DOI: 10.1016/j.ajoc.2022.101315
Incidence of Leber hereditary optic neuropathy in 2019 in Japan: a second nationwide
questionnaire survey
Takano F, Ueda K, Godefrooij DA, Yamagami A, Ishikawa H, Chuman H, Ishikawa H, Ikeda Y, Sakamoto T,
Nakamura M
Orphanet J Rare Dis. 17(1):319,2022
DOI: 10.1186/s13023-022-02478-4
Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan.
Oishi A, Fujinami K, Mawatari G, Naoi N, Ikeda Y, Ueno S, Kuniyoshi K, Hayashi T, Kondo H, Mizota A,
Shinoda K, Kusuhara S, Nakamura M, Iwata T, Tsujikawa A, Tsunoda K.
Genes (Basel). 12(11):1817,2021
DOI: 10.3390/genes12111817
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and
Japanese Patients.
Murakami Y, Koyanagi Y, Fukushima M, Yoshimura M, Fujiwara K, Akiyama M, Momozawa Y, Ueno S, Terasaki
H, Oishi A, Miyata M, Ikeda H, Tsujikawa A, Mizobuchi K, Hayashi T, Fujinami K, Tsunoda K, Park JY, Han
J, Kim M, Lee CS, Kim SJ, Park TK, Joo K, Woo SJ, Ikeda Y, Sonoda KH.
Ophthalmol Retina. 5(12):1269-1279,2021
DOI: 10.1016/j.oret.2021.02.009
Regional differences in genes and variants causing retinitis pigmentosa in Japan.
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M,
Murakami Y, Komori S, Gao D, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y,
Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH.
Jpn J Ophthalmol. 65(3):338-343,2021
DOI: 10.1007/s10384-021-00824-w
A hypomorphic variant in EYS detected by genome-wide association study contributes toward
retinitis pigmentosa.
Nishiguchi KM, Miya F, Mori Y, Fujita K, Akiyama M, Kamatani T, Koyanagi Y, Sato K, Takigawa T, Ueno S,
Tsugita M, Kunikata H, Cisarova K, Nishino J, Murakami A, Abe T, Momozawa Y, Terasaki H, Wada Y, Sonoda
KH, Rivolta C, Tsunoda T, Tsujikawa M, Ikeda Y, Nakazawa T
Commun Biol. 4(1):140,2021
DOI: 10.1038/s42003-021-01662-9
Intravenous immunoglobulin treatment for steroid-resistant optic neuritis: a multicenter,
double-blind, randomized, controlled phase III study
Mimura O, Ishikawa H, Kezuka T, Shikishima K, Suzuki T, Nakamura M, Chuman H, Inoue K, Kimura A,
Yamagami A, Mihoya M, Nakao Y
Jap J Ophthalmol. 65(1):122-132,2021
DOI: 10.1007/s10384-020-00790-9
Association of Rare CYP39A1 Variants with Exfoliation Syndrome Involving the Anterior
Chamber of the Eye
Li Z, Wang Z, Lee MH, Zenkel M, Peh E, Ozaki M, Topouzis F, Nakano S, Chan A, Chen S, Williams SEI, Orr
A, Nakano M, Kobakhidze N, Zarnowski T, Popa-Cherecheanu A, Mizoguchi T, Manabe S, Hayashi K, Kazama S,
Inoue K, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Ideta R, Ishiko S, Yoshida A, Tokumo K,
Kiuchi Y, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Aihara M, Inatani M, Mori K, Ikeda Y, Ueno M,
Gaston D, Rafuse P, Shuba L, Saunders J, Nicolela M, Chichua G, Tabagari S, Founti P, Sim KS, Meah WY,
Soo HM, Chen XY, Chatzikyriakidou A, Keskini C, Pappas T, Anastasopoulos E, Lambropoulos A, Panagiotou
ES, Mikropoulos DG, Kosior-Jarecka E, Cheong A, Li Y, Lukasik U, Nongpiur ME, Husain R, Perera SA,
Álvarez L, García M, González-Iglesias H, Cueto AFV, Cueto LFV, Martinón-Torres F, Salas A, Oguz C,
Tamcelik N, Atalay E, Batu B, Irkec M, Aktas D, Kasım B, Astakhov YS, Astakhov SY, Akopov EL, Giessl A,
Mardin C, Hellerbrand C, Bailey JNC, Igo J RP, Haines JL, Edward DP, Heegaard S, Davila S, Tan P, Kang
JH, Pasquale LR, Kruse FE, Reis A, Carmichael TR, Hauser M, Ramsay M, Mossböck G, Yildirim N, Tashiro K,
Konstas AGP, Coca-Prados M, Foo JN, Kinoshita S, Sotozono C, Kubota T, Dubina M, Ritch R, Wiggs JL,
Pasutto F, Schlötzer-Schrehardt U, Ho YS, Aung T, Tam WL, and Khor CC
JAMA. 325(8):753-764,2021
DOI: 10.1001/jama.2021.0507
日本網膜色素変性レジストリプロジェクトに登録されたデータの解析
池田康博、山本修一、村上晶、高橋政代、川崎良、西口康二、坂本泰二、山下英俊
日眼会誌. 125(4):425-430,2021
網膜色素変性患者における視機能評価とquality of lifeの関係
斉之平真弓、山下高明、寺崎寛人、園田祥三、宮田和典、加茂純子、森本壮、不二門尚、遠藤高生、村上祐介、池田康博、坂本泰二.
日眼会誌. 124: 63-69, 2020.
Base Curve of Progressive Addition Lenses Influences Clear Vision and Stereopsis Area
Mawatari G, Uchida S, Nao-i N
Clin Optom (Auckl). 12:223-230,2020
doi: 10.2147/OPTO.S282326
Effect of Topical Dorzolamide on Cystoid Macular Edema in Retinitis Pigmentosa
Shimokawa S, Fujiwara K, Murakami Y, Funatsu J, Nakatake S, Yoshida N, Sonoda KH, Ikeda Y
Ophthalmol Retina. 4(10):1036-1039, 2020
DOI: 10.1016/j.oret.2020.05.012
Changes of Serum Inflammatory Molecules and Their Relationships with Visual Function in
Retinitis Pigmentosa
Okita A, Murakami Y, Shimokawa S, Funatsu J, Fujiwara K, Nakatake S, Koyanagi Y, Akiyama M, Takeda A,
Hisatomi T, Ikeda
Y, Sonoda KH
Invest Ophthalmol Vis Sci. 61(11):30, 2020
DOI: 10.1167/iovs.61.11.30
Relationship Between Macular Curvature and Common Causative Genes of Retinitis Pigmentosa
in Japanese Patients
Koyanagi Y, Ueno S, Ito Y, Kominami T, Komori S, Akiyama M, Murakami Y, Ikeda Y, Sonoda KH, Terasaki H
Invest Ophthalmol Vis Sci. 61(10):6, 2020
DOI: 10.1167/iovs.61.10.6
Association of CRX genotypes and retinal phenotypes confounded by variable expressivity
and
electronegative electroretinogram
Nishiguchi KM, Kunikata H, Fujita K, Hashimoto K, Koyanagi Y, Akiyama M, Ikeda Y, Momozawa Y, Sonoda
KH,
Murakami A, Wada Y, Nakazawa T
Clin Exp Ophthalmol. 48(5):644-657, 2020
DOI: 10.1111/ceo.13743
A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa
Nishiguchi KM, Fujita K, Ikeda Y, Kunikata H, Koyanagi Y, Akiyama M, Abe T, Wada Y, Sonoda KH, Nakazawa
T
Jpn J Ophthalmol. 64(4):346-350, 2020
DOI: 10.1007/s10384-020-00732-5
Aqueous Flare and Progression of Visual Field Loss in Patients With Retinitis Pigmentosa
Fujiwara K, Ikeda Y, Murakami Y, Tachibana T, Funatsu J, Koyanagi Y, Nakatake S, Shimokawa S, Yoshida
N,
Nakao S,
Hisatomi T, Ishibashi T, Sonoda KH
Invest Ophthalmol Vis Sci.61(8):26, 2020
DOI: 10.1167/iovs.61.8.26
Serous retinal detachment accompanied by pachychoroid in hypotony maculopathy after
trabeculectomy for diabetic
neovascular glaucoma
Shimokawa S, Nakao S, Murakami Y, Ikeda Y, Sonoda KH
Am J Ophthalmol Case Rep. 18:100682, 2020
DOI: 10.1016/j.ajoc.2020.100682
Direct comparison of retinal structure and function in retinitis pigmentosa by
co-registering microperimetry and optical
coherence tomography.
Funatsu J, Murakami Y, Nakatake S, Akiyama M, Fujiwara K, Shimokawa S, Tachibana T, Hisatomi T,
Koyanagi Y, Momozawa Y,
Sonoda KH, Ikeda Y.
PLoS One. 14: e0226097, 2019.
Genetic LAMP2 deficiency accelerates the age-associated formation of basal laminar
deposits in the retina.
Notomi S, Ishihara K, Efstathiou NE, Lee JJ, Hisatomi T, Tachibana T, Konstantinou EK, Ueta T, Murakami
Y, Maidana DE,
Ikeda Y, Kume S, Terasaki H, Sonoda S, Blanz J, Young L, Sakamoto T, Sonoda KH, Saftig P, Ishibashi T,
Miller JW,
Kroemer G, Vavvas DG.
Proc Natl Acad Sci U S A. 116: 23724-23734, 2019.
Relationships Between Serum Antioxidant and Oxidant Statuses and Visual Function in
Retinitis Pigmentosa.
Ishizu M, Murakami Y, Fujiwara K, Funatsu J, Shimokawa S, Nakatake S, Tachibana T, Hisatomi T, Koyanagi
Y, Akiyama M,
Momozawa Y, Ishibashi T, Sonoda KH, Ikeda Y.
Invest Ophthalmol Vis Sci. 60: 4462-4468, 2019.
Capillary Dropout is Dominant in Deep Capillary Plexus in Early Diabetic Retinopathy in
Optical Coherence Tomography
Angiography.
Kaizu Y, Nakao S, Arima M, Wada I, Yamaguchi M, Sekiryu H, Hayami T, Ishikawa K, Ikeda Y, Sonoda KH.
Acta Ophthalmol, 97: e811-e812, 2019.
Early detection of cone photoreceptor cell loss in retinitis pigmentosa using adaptive
optics scanning laser
ophthalmoscopy.
Nakatake S, Murakami Y, Funatsu J, Koyanagi Y, Akiyama M, Momozawa Y, Ishibashi T, Sonoda KH, Ikeda Y.
Graefes Arch Clin Exp Ophthalmol. 257: 1169-1181, 2019.
Effect of Ocular Hypertension on D- β -Aspartic Acid-Containing Proteins in the Retinas
of Rats.
Kanamoto T, Tachibana T, Kiyota Y, Hisatomi T, Ikeda Y, Murakami Y, Tobiume K, Asaoka R, Kiuchi Y.
J Ophthalmol. 2019: 2431481, 2019.
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending
the RP1 Disease Spectrum.
Verbakel SK, van Huet RAC, den Hollander AI, Geerlings MJ, Kersten E, Klevering BJ, Klaver CCW, Plomp
AS, Wesseling NL,
Bergen AAB, Nikopoulos K, Rivolta C, Ikeda Y, Sonoda KH, Wada Y, Boon CJF, Nakazawa T, Hoyng
CB, Nishiguchi KM.
Invest Ophthalmol Vis Sci. 60: 1192-1203, 2019.
Development of a novel noninvasive system for measurement and imaging of the arterial
phase oxygen density ratio in the
retinal microcirculation.
Ishikawa S, Yoshinaga Y, Kantake D, Nakamura D, Yoshida N, Hisatomi T, Ikeda Y, Ishibashi T, Enaida H.
Graefes Arch Clin Exp Ophthalmol. 257: 557-565, 2019.
Night-vision aid using see-through display for patients with retinitis pigmentosa.
Ikeda Y, Nakatake S, Funatsu J, Fujiwara K, Tachibana T, Murakami Y, Hisatomi T, Yoshida S, Enaida H,
Ishibashi T,
Sonoda KH.
Jpn J Ophthalmol. 63: 181-185, 2019.
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 Y-F, Komori S, Ueno S, Terasaki H, Katagiri
S, Hayashi T, Kuniyoshi K, Miyake Y, Tsunoda K, Yoshitake K, Iwata T, Nao-i N, on behalf of
the JEGC study group
Human Genome Variation. 6(1): 34, 2019
DOI: 10.1038/s41439-019-0065-7
A frequent variant in the Japanese population determines quasi-Mendelian
inheritance of rare retinal ciliopathy
Nikopoulos K, Cisarova K, Quinodoz M, Koskiniemi-Kuendig H, Miyake N, Farinelli P, Rehman AU,
Khan MI, Prunotto A, Akiyama M, Kamatani Y, Terao C, Miya F, Ikeda Y, Ueno S, Fuse N,
Murakami A, Wada Y, Terasaki H, Sonoda KH, Ishibashi T, Kubo M, Cremers FPM, Kutalik Z,
Matsumoto N, Nishiguchi KM, Nakazawa T, Rivolta C
Nat Commun. 10(1): 2884, 2019
DOI: 10.1038/s41467-019-10746-4
Flow Density in Optical Coherence Tomography Angiography is Useful for
Retinopathy Diagnosis in Diabetic Patients
Kaizu Y, Nakao S, Arima M, Hayami T, Wada I, Yamaguchi M, Sekiryu H, Ishikawa K, Ikeda Y,
Sonoda KH
Sci Rep. 9(1): 8668, 2019
DOI: 10.1038/s41598-019-45194-z
Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with
S-Antigen Mutations: A Long-Term Follow-up Study
Nishiguchi KM, Ikeda Y, Fujita K, Kunikata H, Akiho M, Hashimoto K, Hosono K, Kurata K,
Koyanagi Y, Akiyama M, Suzuki T, Kawasaki R, Wada Y, Hotta Y, Sonoda KH, Murakami A,
Nakazawa M, Nakazawa T, Abe T
Ophthalmology. 126:1557-1566, 2019
DOI: 10.1016/j.ophtha.2019.05.027
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y,
Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K,
Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M,
Sonoda KH
J Med Genet. 56(10): 662-670, 2019
DOI: 10.1136/jmedgenet-2018-105691