S. Nishina

发表

Surgical treatments for fibrous tissue extending to the posterior retina in eyes with familial exudative vitreoretinopathy

Mari Takahashi, T. Yokoi, S. Katagiri, 2017, Japanese Journal of Ophthalmology.

Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells

Tadashi Yokoi, Taku Tanaka, T. Yokoi, 2015, Scientific Reports.

Clinical Features of Anterior Segment Dysgenesis Associated With Congenital Corneal Opacities

T. Yokoi, S. Nishina, N. Azuma, 2012, Cornea.

Anteroposterior Patterning of Gene Expression in the Human Infant Sclera: Chondrogenic Potential and Wnt Signaling

M. Toyoda, D. Kami, A. Umezawa, 2017, Current eye research.

The clock components Period2, Cryptochrome1a, and Cryptochrome2a function in establishing light-dependent behavioral rhythms and/or total activity levels in zebrafish

H. Nishina, K. Nakahama, N. Takamatsu, 2019, Scientific Reports.

Different foveal schisis patterns in each retinal layer in eyes with hereditary juvenile retinoschisis evaluated by en-face optical coherence tomography

T. Yokoi, S. Katagiri, Tomoyo Yoshida-Uemura, 2017, Graefe's Archive for Clinical and Experimental Ophthalmology.

CD44 expression in the developing human retina

T. Hida, S. Nishina, N. Azuma, 1997, Graefe's Archive for Clinical and Experimental Ophthalmology.

Evaluation of scleral buckling for stage 4A retinopathy of prematurity by fluorescein angiography.

T. Yokoi, S. Nishina, N. Azuma, 2009, American journal of ophthalmology.

Congenital rotated macula with good vision and binocular function

T. Yokoi, S. Nishina, N. Azuma, 2009, Japanese Journal of Ophthalmology.

Use of the Delphi process in paediatric cataract management

P. Nucci, A. Levin, R. Kekunnaya, 2015, British Journal of Ophthalmology.

A de novo deletion of 20q11.2–q12 in a boy presenting with abnormal hands and feet, retinal dysplasia, and intractable feeding difficulty

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2011, American journal of medical genetics. Part A.

The mevalonate pathway regulates primitive streak formation via protein farnesylation

H. Nishina, J. Penninger, H. Kagechika, 2016, Scientific Reports.

Ophthalmic features of CHARGE syndrome with CHD7 mutations

R. Kosaki, K. Kosaki, N. Okamoto, 2012, American journal of medical genetics. Part A.

Surgical Treatment of Recurrent Juvenile Xanthogranuloma of the Eyelid

S. Nishina, N. Azuma, J. Miyauchi, 2004, Japanese Journal of Ophthalmology.

Is a 6-week course of ganciclovir therapy effective for chorioretinitis in infants with congenital cytomegalovirus infection?

N. Inoue, A. Saitoh, S. Nishina, 2010, The Journal of pediatrics.

Clinical features of a toddler with bilateral bullous retinoschisis with a novel RS1 mutation

K. Kadonosono, Takaaki Hayashi, T. Yokoi, 2016, American journal of ophthalmology case reports.

PAX6 missense mutation in isolated foveal hypoplasia

M. Yamada, T. Okuyama, S. Nishina, 1996, Nature Genetics.

Fluorescein Staining of the Vitreous During Vitrectomy for Retinopathy of Prematurity

T. Yokoi, S. Nishina, N. Azuma, 2011, Retina.

Severe macular pucker after retinal detachment surgery in an infant

S. Nishina, N. Azuma, 2002, The British journal of ophthalmology.

Endogenous candida chorioretinitis in a healthy infant

S. Sugita, Makiko Ito, T. Yokoi, 2010, Japanese Journal of Ophthalmology.

Three cases of rhegmatogenous retinal detachment associated with regressed retinoblastoma after conservative tumor therapy.

K. Matsuoka, Makiko Ito, T. Yokoi, 2014, Retinal cases & brief reports.

Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism

S. Minoshima, M. Ohtsubo, Miho Sato, 2020, Journal of Human Genetics.

Concurrent deletion of BMP4 and OTX2 genes, two master genes in ophthalmogenesis.

R. Kosaki, K. Kosaki, T. Takenouchi, 2013, European journal of medical genetics.

Survey of microphthalmia in Japan

Y. Nishida, D. Kurosaka, S. Nishina, 2012, Japanese Journal of Ophthalmology.

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

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

Surgical outcomes of progressive tractional retinal detachment associated with familial exudative vitreoretinopathy.

T. Yokoi, S. Nishina, N. Azuma, 2014, American journal of ophthalmology.

Visual outcomes after early vitreous surgery for aggressive posterior retinopathy of prematurity.

Makiko Ito, T. Yokoi, S. Nishina, 2013, JAMA ophthalmology.

Early vitreous surgery for aggressive posterior retinopathy of prematurity.

S. Nishina, N. Azuma, K. Ishikawa, 2006, American journal of ophthalmology.

Genotype–phenotype correlation of PAX6 gene mutations in aniridia

T. Ogata, T. Yokoi, S. Nishina, 2016, Human Genome Variation.

PAX6 expression in the developing human eye

H. Handa, Y. Yamaguchi, S. Kohsaka, 1999, The British journal of ophthalmology.

Incidence of side effects of topical atropine sulfate and cyclopentolate hydrochloride for cycloplegia in Japanese children: a multicenter study

T. Fujikado, Takao Hayashi, Miho Sato, 2018, Japanese Journal of Ophthalmology.

Fat adherence syndrome after retinal surgery treated with amniotic membrane transplantation.

K. Shinoda, S. Nishina, M. Yamada, 2001, American journal of ophthalmology.

Pax6-5a promotes neuronal differentiation of murine embryonic stem cells.

T. Katada, T. Iwatsubo, H. Nishina, 2009, Biological & pharmaceutical bulletin.

p38 Mitogen-activated protein kinase controls a switch between cardiomyocyte and neuronal commitment of murine embryonic stem cells by activating myocyte enhancer factor 2C-dependent bone morphogenetic protein 2 transcription.

H. Kajiho, T. Katada, H. Nishina, 2010, Stem cells and development.

Generation of Retinal Ganglion Cells With Functional Axons From Mouse Embryonic Stem Cells and Induced Pluripotent Stem Cells.

T. Yokoi, S. Nishina, N. Azuma, 2016, Investigative ophthalmology & visual science.

Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: A clinical report and review of literature

Y. Fukushima, R. Kosaki, Y. Aoki, 2014, American journal of medical genetics. Part A.

Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism

S. Minoshima, M. Ohtsubo, Miho Sato, 2020, Journal of human genetics.

Effects of neuroactive agents on axonal growth and pathfinding of retinal ganglion cells generated from human stem cells

T. Yokoi, S. Nishina, N. Azuma, 2017, Scientific Reports.

Gorham-Stout syndrome affecting the temporal bone with cerebrospinal fluid leakage.

S. Nishina, N. Morimoto, A. Nakazawa, 2013, International journal of pediatric otorhinolaryngology.

Structure of the Retinal Margin and Presumed Mechanism of Retinal Detachment in Choroidal Coloboma.

T. Yokoi, S. Katagiri, Tomoyo Yoshida-Uemura, 2020, Ophthalmology. Retina.

Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population

Shinsei Minoshima, Miho Sato, Tadashi Yokoi, 2012, PloS one.

Successful scleral buckling of late-onset visual decrease in eye with retinal folds

T. Yokoi, S. Katagiri, S. Nishina, 2016, Documenta Ophthalmologica.

Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome

T. Ogata, K. Kosaki, H. Saitsu, 2021, Journal of Human Genetics.

Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations

Miho Sato, T. Yokoi, S. Nishina, 2019, Human Genome Variation.

Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations

Miho Sato, T. Yokoi, S. Nishina, 2019, Human Genome Variation.

The clock components Period2, Cryptochrome1a, and Cryptochrome2a function in establishing light-dependent behavioral rhythms and/or total activity levels in zebrafish

H. Nishina, K. Nakahama, N. Takamatsu, 2019, Scientific Reports.

ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISK REGION

T. Yokoi, S. Katagiri, S. Nishina, 2017, Retina.

Vascular abnormalities in aggressive posterior retinopathy of prematurity detected by fluorescein angiography.

T. Yokoi, S. Nishina, N. Azuma, 2009, Ophthalmology.

Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene

K. Fujiki, A. Kanai, M. Hayakawa, 1998, Human Genetics.

Japanese juvenile retinoschisis is caused by mutations of the

K. Fujiki, A. Kanai, M. Hayakawa, 1998 .

[Prolonged optic disc swelling in Kawasaki disease - A case report and literature review].

H. Ono, A. Ishiguro, J. Abe, 2017, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers

Miho Sato, Takaaki Hayashi, T. Nakano, 2019, International journal of molecular sciences.

Exudative retinal detachment following cataract surgery in Hallermann-Streiff syndrome

S. Nishina, N. Azuma, Yumi Suzuki, 2008, Graefe's Archive for Clinical and Experimental Ophthalmology.

Long-term surgical outcome of conventional trabeculotomy for childhood glaucoma

E. Inoue, T. Yokoi, S. Katagiri, 2017, Japanese Journal of Ophthalmology.

Outcome of early surgery for bilateral congenital cataracts in eyes with microcornea.

S. Nishina, N. Azuma, E. Noda, 2007, American journal of ophthalmology.

Nishida’s procedure combined with medial rectus recession for large-angle esotropia in Duane syndrome

S. Nishina, N. Azuma, Michiko Tanaka, 2011, Japanese Journal of Ophthalmology.

Rectus eye muscle paths after surgical correction of convergent strabismus fixus.

S. Nishina, M. Yamada, S. Satofuka, 2002, American journal of ophthalmology.

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

Y. Wada, S. Nomura, T. Ogata, 2022, Genes.

Clinical features of congenital retinal folds.

T. Yokoi, S. Nishina, N. Azuma, 2012, American journal of ophthalmology.

Risk factors for recurrent fibrovascular proliferation in aggressive posterior retinopathy of prematurity after early vitreous surgery.

T. Yokoi, S. Nishina, N. Azuma, 2010, American journal of ophthalmology.

Retinal Structure and Function in Eyes with Optic Nerve Hypoplasia

T. Yokoi, S. Katagiri, S. Nishina, 2017, Scientific Reports.

Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy

Yoko Fukushima, M. Kondo, T. Yokoi, 2016, Scientific Reports.

Structure and Morphology of Radial Retinal Folds with Familial Exudative Vitreoretinopathy.

T. Yokoi, S. Katagiri, S. Nishina, 2016, Ophthalmology.

Outer retinal deformity detected by optical coherence tomography in eyes with foveal hypoplasia

T. Yokoi, S. Katagiri, S. Nishina, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

Characteristics of Retinal Breaks and Surgical Outcomes in Rhegmatogenous Retinal Detachment in Familial Exudative Vitreoretinopathy.

T. Yokoi, S. Katagiri, Tomoyo Yoshida-Uemura, 2017, Ophthalmology. Retina.

Scleral window surgery and topical mitomycin C for nanophthalmic uveal effusion complicated by renal failure: case report

S. Nishina, N. Azuma, Yumi Suzuki, 2007, Graefe's Archive for Clinical and Experimental Ophthalmology.

Axial spondylometaphyseal dysplasia: Additional reports

Y. Makita, T. Cho, K. Fujieda, 2011, American journal of medical genetics. Part A.

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

S. Minoshima, H. Saitsu, Miho Sato, 2018, Scientific Reports.

Effect of early vitreous surgery for aggressive posterior retinopathy of prematurity detected by fundus fluorescein angiography.

T. Yokoi, S. Nishina, N. Azuma, 2009, Ophthalmology.

Abnormal traction of the vitreous detected by swept-source optical coherence tomography is related to the maculopathy associated with optic disc pits

T. Yokoi, S. Nishina, N. Azuma, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

Two patients with different features of congenital optic disc anomalies in the two eyes

S. Nishina, N. Azuma, Yumi Suzuki, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

National survey of amblyopia treatment in Japan: comparison with amblyopia treatment study results of the pediatric eye disease investigator group

A. Miki, S. Nishina, Tsuyoshi Yoneda, 2022, Japanese Journal of Ophthalmology.

Glial extrusion from regressed retinoblastoma after conservative treatment

K. Matsuoka, T. Yokoi, S. Nishina, 2008, Acta ophthalmologica.

Early laser photocoagulation for extensive retinal avascularity in infants with incontinentia pigmenti

T. Yokoi, S. Nishina, N. Azuma, 2020, Japanese Journal of Ophthalmology.

SEVERE RECURRENT FIBROVASCULAR PROLIFERATION AFTER COMBINED INTRAVITREAL BEVACIZUMAB INJECTION AND LASER PHOTOCOAGULATION FOR AGGRESSIVE POSTERIOR RETINOPATHY OF PREMATURITY

T. Yokoi, S. Katagiri, S. Nishina, 2019, Retinal cases & brief reports.

Effects of neuroactive agents on axonal growth and pathfinding of retinal ganglion cells generated from human stem cells

T. Yokoi, S. Nishina, N. Azuma, 2017, Scientific Reports.

A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene

H. Saitsu, M. Kosuga, T. Yokoi, 2023, Human Genome Variation.

Development of a premacular vitreous pocket.

T. Yokoi, S. Nishina, N. Azuma, 2013, JAMA ophthalmology.

The role of vitreoretinal traction in the pathogenesis of maculopathy associated with optic disc pits

T. Yokoi, S. Nishina, N. Azuma, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

CrxOS maintains the self-renewal capacity of murine embryonic stem cells.

H. Kajiho, T. Katada, H. Nishina, 2009, Biochemical and biophysical research communications.

Atypical intravitreal growth of retinoblastoma with a multi-branching configuration

T. Yokoi, S. Katagiri, S. Nishina, 2017, American journal of ophthalmology case reports.

Case of aggressive posterior retinopathy of prematurity with atypical neovascular growth

K. Matsuoka, S. Nishina, N. Azuma, 2008, Japanese Journal of Ophthalmology.

Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes

K. Higasa, T. Sakamoto, Takaaki Hayashi, 2024, Ophthalmology science.

Retinal hemorrhages and damages from tractional forces associated with infantile abusive head trauma evaluated by wide-field fundus photography

T. Yokoi, S. Nishina, M. Miyasaka, 2024, Scientific reports.