138 related articles for article (PubMed ID: 38288273)
1. Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series.
Feng C; Chen Q; Luan X; Sun P; Cao Y; Wu J; Wang S; Sun X; Cao L; Tian G
Front Med (Lausanne); 2024; 11():1188193. PubMed ID: 38288273
[TBL] [Abstract][Full Text] [Related]
2. Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene.
Nakamura N; Tsunoda K; Mitsutake A; Shibata S; Mano T; Nagashima Y; Ishiura H; Iwata A; Toda T; Tsuji S; Sawamura H
Invest Ophthalmol Vis Sci; 2020 Sep; 61(11):27. PubMed ID: 32931575
[TBL] [Abstract][Full Text] [Related]
3. NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment.
Sone J; Ueno S; Akagi A; Miyahara H; Tamai C; Riku Y; Yabata H; Koizumi R; Hattori T; Hirose H; Koyanagi Y; Kobayashi R; Okada H; Kishimoto Y; Hashizume Y; Sobue G; Yoshida M; Iwasaki Y
Acta Neuropathol Commun; 2023 May; 11(1):71. PubMed ID: 37131242
[TBL] [Abstract][Full Text] [Related]
4. Full-field ERG as a predictor of the natural course of
Schroeder M; Kjellström U
Mol Vis; 2018; 24():1-16. PubMed ID: 29386879
[TBL] [Abstract][Full Text] [Related]
5. Characteristics of ocular findings of patients with neuronal intranuclear inclusion disease.
Liu C; Luan X; Liu X; Wang X; Cai X; Li T; Cao L; Long D
Neurol Sci; 2022 May; 43(5):3231-3237. PubMed ID: 34797461
[TBL] [Abstract][Full Text] [Related]
6. 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; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
[TBL] [Abstract][Full Text] [Related]
7. Recurrent episodes of night blindness in a patient with short bowel syndrome.
Renner AB; Dietrich-Ntoukas T; Jägle H
Doc Ophthalmol; 2015 Dec; 131(3):221-30. PubMed ID: 26507840
[TBL] [Abstract][Full Text] [Related]
8. [Fundus features of nanophthalmos analyzed by optical coherence tomography].
Xiao H; Liu X; Zhong YM; Guo XX; Mi L; Li M
Zhonghua Yan Ke Za Zhi; 2013 Dec; 49(12):1069-74. PubMed ID: 24499692
[TBL] [Abstract][Full Text] [Related]
9. Case of adult-onset neuronal intranuclear hyaline inclusion disease with negative electroretinogram.
Yamada W; Takekoshi A; Ishida K; Mochizuki K; Sone J; Sobue G; Hayashi Y; Inuzuka T; Miyake Y
Doc Ophthalmol; 2017 Jun; 134(3):221-226. PubMed ID: 28332008
[TBL] [Abstract][Full Text] [Related]
10. Wide-field fundus autofluorescence abnormalities and visual function in patients with cone and cone-rod dystrophies.
Oishi M; Oishi A; Ogino K; Makiyama Y; Gotoh N; Kurimoto M; Yoshimura N
Invest Ophthalmol Vis Sci; 2014 May; 55(6):3572-7. PubMed ID: 24845635
[TBL] [Abstract][Full Text] [Related]
11. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
[TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
[TBL] [Abstract][Full Text] [Related]
13. Acute Zonal Cone Photoreceptor Outer Segment Loss.
Aleman TS; Sandhu HS; Serrano LW; Traband A; Lau MK; Adamus G; Avery RA
JAMA Ophthalmol; 2017 May; 135(5):487-490. PubMed ID: 28384671
[TBL] [Abstract][Full Text] [Related]
14. Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.
van Huet RA; Estrada-Cuzcano A; Banin E; Rotenstreich Y; Hipp S; Kohl S; Hoyng CB; den Hollander AI; Collin RW; Klevering BJ
Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4683-90. PubMed ID: 23788369
[TBL] [Abstract][Full Text] [Related]
15. Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography.
Park SJ; Woo SJ; Park KH; Hwang JM; Chung H
Invest Ophthalmol Vis Sci; 2010 Jul; 51(7):3673-9. PubMed ID: 20164460
[TBL] [Abstract][Full Text] [Related]
16. Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.
Cho SC; Woo SJ; Park KH; Hwang JM
Korean J Ophthalmol; 2013 Feb; 27(1):19-27. PubMed ID: 23372375
[TBL] [Abstract][Full Text] [Related]
17. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
van Huet RA; Collin RW; Siemiatkowska AM; Klaver CC; Hoyng CB; Simonelli F; Khan MI; Qamar R; Banin E; Cremers FP; Theelen T; den Hollander AI; van den Born LI; Klevering BJ
Invest Ophthalmol Vis Sci; 2014 May; 55(6):3939-53. PubMed ID: 24876279
[TBL] [Abstract][Full Text] [Related]
18. Two cases of unilateral cone-rod dysfunction with negative electroretinograms.
Ozawa K; Takahashi S; Mochizuki K; Miyake Y
Doc Ophthalmol; 2019 Dec; 139(3):247-256. PubMed ID: 31375969
[TBL] [Abstract][Full Text] [Related]
19. Bardet-Biedl syndrome-7 (
Aleman TS; O'Neil EC; O'Connor K; Jiang YY; Aleman IA; Bennett J; Morgan JIW; Toussaint BW
Ophthalmic Genet; 2021 Jun; 42(3):252-265. PubMed ID: 33729075
[No Abstract] [Full Text] [Related]
20. Retinal dysfunction in a presymptomatic patient with Huntington's disease.
Knapp J; VanNasdale DA; Ramsey K; Racine J
Doc Ophthalmol; 2018 Jun; 136(3):213-221. PubMed ID: 29691705
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
