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High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1).
- Published in:
- Documenta Ophthalmologica, 2021, v. 142, n. 1, p. 87, doi. 10.1007/s10633-020-09782-z
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- Publication type:
- Article
Improvement of reduced electroretinographic responses in thymoma-associated retinopathy: a case report and literature review.
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- Documenta Ophthalmologica, 2020, v. 141, n. 2, p. 195, doi. 10.1007/s10633-020-09764-1
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- Publication type:
- Article
Novel biallelic splice-site BBS1 variants in Bardet–Biedle syndrome: a case report of the first Japanese patient.
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- Documenta Ophthalmologica, 2020, v. 141, n. 1, p. 77, doi. 10.1007/s10633-020-09752-5
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- Publication type:
- Article
Electroretinographic abnormalities associated with pregabalin: a case report.
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- Documenta Ophthalmologica, 2020, v. 140, n. 3, p. 279, doi. 10.1007/s10633-019-09743-1
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- Publication type:
- Article
Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
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- Documenta Ophthalmologica, 2020, v. 140, n. 2, p. 147, doi. 10.1007/s10633-019-09727-1
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- Publication type:
- Article
Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.
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- Documenta Ophthalmologica, 2019, v. 138, n. 3, p. 229, doi. 10.1007/s10633-019-09679-6
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- Publication type:
- Article
Successful scleral buckling of late-onset visual decrease in eye with retinal folds.
- Published in:
- Documenta Ophthalmologica, 2016, v. 133, n. 2, p. 145, doi. 10.1007/s10633-016-9559-5
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- Publication type:
- Article
Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
- Published in:
- Documenta Ophthalmologica, 2015, v. 130, n. 3, p. 189, doi. 10.1007/s10633-015-9488-8
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- Publication type:
- Article
Multimodal imaging of a case of peripheral cone dystrophy.
- Published in:
- Documenta Ophthalmologica, 2015, v. 130, n. 3, p. 241, doi. 10.1007/s10633-015-9490-1
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- Publication type:
- Article
The first Japanese family of CDH3‐related hypotrichosis with juvenile macular dystrophy.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 6, p. 1, doi. 10.1002/mgg3.1688
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- Publication type:
- Article
Association of meteorological factors with the frequency of primary rhegmatogenous retinal detachment in Japan.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-88979-x
- By:
- Publication type:
- Article
Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Autosomal dominant retinitis pigmentosa with macular involvement associated with a disease haplotype that included a novel <italic>PRPH2</italic> variant (p.Cys250Gly).
- Published in:
- Ophthalmic Genetics, 2018, v. 39, n. 3, p. 357, doi. 10.1080/13816810.2018.1459737
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- Publication type:
- Article
A novel homozygous CYP4V2 variant (p.S121Y) associated with a choroideremia-like phenotype.
- Published in:
- Ophthalmic Genetics, 2017, v. 38, n. 3, p. 286, doi. 10.1080/13816810.2016.1193880
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- Publication type:
- Article
A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy.
- Published in:
- Ophthalmic Genetics, 2016, v. 37, n. 3, p. 354, doi. 10.3109/13816810.2015.1066829
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- Publication type:
- Article
RPE65 Mutations in Two Japanese Families with Leber Congenital Amaurosis.
- Published in:
- Ophthalmic Genetics, 2016, v. 37, n. 2, p. 161, doi. 10.3109/13816810.2014.991931
- By:
- Publication type:
- Article
Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.
- Published in:
- Ophthalmic Genetics, 2016, v. 37, n. 1, p. 68, doi. 10.3109/13816810.2014.949380
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- Publication type:
- Article
Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).
- Published in:
- Ophthalmic Genetics, 2015, v. 36, n. 2, p. 137, doi. 10.3109/13816810.2014.991932
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- Publication type:
- Article
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1331, doi. 10.3390/ijms21041331
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- Publication type:
- Article
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 6, p. 1518, doi. 10.3390/ijms20061518
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- Publication type:
- Article
Impact of hepatectomy for huge solitary hepatocellular carcinoma.
- Published in:
- Journal of Surgical Oncology, 2013, v. 107, n. 4, p. 408, doi. 10.1002/jso.23226
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- Publication type:
- Article
Mass-forming intrahepatic cholangiocarcinoma with marked enhancement on arterial-phase computed tomography reflects favorable surgical outcomes.
- Published in:
- Journal of Surgical Oncology, 2011, v. 104, n. 2, p. 130, doi. 10.1002/jso.21917
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- Publication type:
- Article
Sectionectomy Is Suitable for Patients with T2 Hepatocellular Carcinoma according to the Modified International Union against Cancer TNM Classification.
- Published in:
- Digestive Surgery, 2007, v. 24, n. 5, p. 342, doi. 10.1159/000107714
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- Publication type:
- Article
Surgical treatments for fibrous tissue extending to the posterior retina in eyes with familial exudative vitreoretinopathy.
- Published in:
- Japanese Journal of Ophthalmology, 2018, v. 62, n. 1, p. 63, doi. 10.1007/s10384-017-0547-4
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- Publication type:
- Article
Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.
- Published in:
- Japanese Journal of Ophthalmology, 2017, v. 61, n. 5, p. 395, doi. 10.1007/s10384-017-0522-0
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- Publication type:
- Article
Long-term surgical outcome of conventional trabeculotomy for childhood glaucoma.
- Published in:
- Japanese Journal of Ophthalmology, 2017, v. 61, n. 3, p. 237, doi. 10.1007/s10384-017-0506-0
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- Publication type:
- Article
Retinal Structure and Function in Eyes with Optic Nerve Hypoplasia.
- Published in:
- Scientific Reports, 2017, p. 42480, doi. 10.1038/srep42480
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- Publication type:
- Article
Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy.
- Published in:
- Scientific Reports, 2016, p. 30523, doi. 10.1038/srep30523
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- Publication type:
- Article
Comparative analysis of complete orthologous centromeres from two subspecies of rice reveals rapid variation of centromere organization and structure.
- Published in:
- Plant Journal, 2009, v. 60, n. 5, p. 805, doi. 10.1111/j.1365-313X.2009.04002.x
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- Publication type:
- Article
Sequencing and characterization of telomere and subtelomere regions on rice chromosomes 1S, 2S, 2L, 6L, 7S, 7L and 8S.
- Published in:
- Plant Journal, 2006, v. 46, n. 2, p. 206, doi. 10.1111/j.1365-313X.2006.02684.x
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- Publication type:
- Article
Technical Advance Physical maps and recombination frequency of six rice chromosomes.
- Published in:
- Plant Journal, 2003, v. 36, n. 5, p. 720, doi. 10.1046/j.1365-313X.2003.01903.x
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- Publication type:
- Article
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.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 3, p. 656, doi. 10.1002/ajmg.c.31826
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- Publication type:
- Article
RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.
- Published in:
- Journal of Ophthalmology, 2014, p. 1, doi. 10.1155/2014/210947
- By:
- Publication type:
- Article
Favorable long-term surgical outcomes of hepatocellular carcinoma in patients with hepatitis B envelope antibody.
- Published in:
- Journal of Surgical Oncology, 2010, v. 101, n. 6, p. 471, doi. 10.1002/jso.21512
- By:
- Publication type:
- Article
The value of anatomical liver sectionectomy for patients with a solitary hepatocellular carcinoma from 2 to 5 cm in greatest diameter.
- Published in:
- Journal of Surgical Oncology, 2009, v. 100, n. 7, p. 585, doi. 10.1002/jso.21363
- By:
- Publication type:
- Article
Intrahepatic cholangiocarcinoma diagnosed preoperatively as hepatocellular carcinoma.
- Published in:
- Journal of Surgical Oncology, 2004, v. 87, n. 2, p. 80, doi. 10.1002/jso.20091
- By:
- Publication type:
- Article
Hepatocellular carcinoma after direct‐acting antiviral drug treatment in patients with hepatitis C virus.
- Published in:
- JGH Open, 2019, v. 3, n. 1, p. 52, doi. 10.1002/jgh3.12105
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- Publication type:
- Article
Spermidine determines the sensitivity to the calmodulin antagonist, chlorpromazine, for the circadian conidiation rhythm but not for the mycelial growth in Neurospora crassa.
- Published in:
- Journal of Biological Rhythms, 1998, v. 13, n. 6, p. 452, doi. 10.1177/074873098129000282
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- Publication type:
- Article
Mutants with altered sensitivity to a calmodulin antagonist affect the circadian clock in...
- Published in:
- Genetics, 1996, v. 143, n. 3, p. 1175, doi. 10.1093/genetics/143.3.1175
- By:
- Publication type:
- Article
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65737-z
- By:
- Publication type:
- Article
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-62119-3
- By:
- Publication type:
- Article
Effectiveness of the Heads-Up Surgery System for Retinal Surgery in a Patient with Severe Photophobia.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Longitudinal follow-up of two patients with isolated paracentral acute middle maculopathy.
- Published in:
- International Medical Case Reports Journal, 2019, v. 12, p. 143, doi. 10.2147/IMCRJ.S196047
- By:
- Publication type:
- Article
A BAC physical map of aus rice cultivar ' Kasalath', and the map-based genomic sequence of ' Kasalath' chromosome 1.
- Published in:
- Plant Journal, 2013, v. 76, n. 4, p. 699, doi. 10.1111/tpj.12317
- By:
- Publication type:
- Article
Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0108721
- By:
- Publication type:
- Article
Occult macular dystrophy with bilateral chronic subfoveal serous retinal detachment associated with a novel RP1L1 mutation (p.S1199P).
- Published in:
- Documenta Ophthalmologica, 2014, v. 129, n. 1, p. 49, doi. 10.1007/s10633-014-9443-0
- By:
- Publication type:
- Article
Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS gene.
- Published in:
- Documenta Ophthalmologica, 2014, v. 128, n. 3, p. 211, doi. 10.1007/s10633-014-9435-0
- By:
- Publication type:
- Article
OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina.
- Published in:
- Documenta Ophthalmologica, 2014, v. 128, n. 2, p. 137, doi. 10.1007/s10633-014-9426-1
- By:
- Publication type:
- Article