These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 35885980)
1. Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy. Kim HR; Han J; Kim YJ; Kang HG; Byeon SH; Kim SS; Lee CS Genes (Basel); 2022 Jul; 13(7):. PubMed ID: 35885980 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy. Wivestad Jansson R; Berland S; Bredrup C; Austeng D; Andréasson S; Wittström E Ophthalmic Genet; 2016 Jun; 37(2):183-93. PubMed ID: 26333019 [TBL] [Abstract][Full Text] [Related]
4. Familial autosomal recessive bestrophinopathy: identification of a novel variant in BEST1 gene and the specific metabolomic profile. Ye P; Xu J; Luo Y; Su Z; Yao K BMC Med Genet; 2020 Jan; 21(1):16. PubMed ID: 31969119 [TBL] [Abstract][Full Text] [Related]
5. A Novel BEST1 Mutation in Autosomal Recessive Bestrophinopathy. Lee CS; Jun I; Choi SI; Lee JH; Lee MG; Lee SC; Kim EK Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):8141-50. PubMed ID: 26720466 [TBL] [Abstract][Full Text] [Related]
6. Clinical and genetic features in autosomal recessive bestrophinopathy in Chinese cohort. Zhao D; Gu VY; Wang Y; Peng J; Lyu J; Fei P; Xu Y; Zhang X; Zhao P BMC Ophthalmol; 2024 Jul; 24(1):308. PubMed ID: 39048936 [TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive bestrophinopathy combined with neurofibromatosis type 1 in a patient. Zhao B; Chen L; Zhang P; He K; Lei M; Zhang J BMC Ophthalmol; 2023 Apr; 23(1):151. PubMed ID: 37041514 [TBL] [Abstract][Full Text] [Related]
9. Novel Missense Mutations in Jaffal L; Joumaa WH; Assi A; Helou C; Condroyer C; El Dor M; Cherfan G; Zeitz C; Audo I; Zibara K; El Shamieh S Genes (Basel); 2019 Feb; 10(2):. PubMed ID: 30781664 [TBL] [Abstract][Full Text] [Related]
10. Novel BEST1 mutations and special clinical characteristics of autosomal recessive bestrophinopathy in Chinese patients. Luo J; Lin M; Guo X; Xiao X; Li J; Hu H; Xiao H; Xu X; Zhong Y; Long S; Luo G; Mi L; Chen X; Fang L; Wei W; Zhang Q; Liu X Acta Ophthalmol; 2019 May; 97(3):247-259. PubMed ID: 30593719 [TBL] [Abstract][Full Text] [Related]
12. Typical best vitelliform dystrophy secondary to biallelic variants in BEST1. Dhoble P; Robson AG; Webster AR; Michaelides M Ophthalmic Genet; 2024 Feb; 45(1):38-43. PubMed ID: 36908234 [TBL] [Abstract][Full Text] [Related]
13. A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy. Haque OI; Chandrasekaran A; Nabi F; Ahmad O; Marques JP; Ahmad T BMC Ophthalmol; 2022 Dec; 22(1):493. PubMed ID: 36527004 [TBL] [Abstract][Full Text] [Related]
14. Novel Soto-Sierra M; Morillo-Sánchez MJ; Martín-Sánchez M; Ramos-Jiménez M; López-Domínguez M; Ponte-Zuñiga B; Antiñolo G; Rodríguez-de-la-Rúa E Eur J Ophthalmol; 2022 Sep; 32(5):NP77-NP81. PubMed ID: 33866859 [TBL] [Abstract][Full Text] [Related]
15. Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy. Pfister TA; Zein WM; Cukras CA; Sen HN; Maldonado RS; Huryn LA; Hufnagel RB Invest Ophthalmol Vis Sci; 2021 May; 62(6):22. PubMed ID: 34015078 [TBL] [Abstract][Full Text] [Related]
16. Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation. Kubota D; Gocho K; Akeo K; Kikuchi S; Sugahara M; Matsumoto CS; Shinoda K; Mizota A; Yamaki K; Takahashi H; Kameya S Doc Ophthalmol; 2016 Jun; 132(3):233-43. PubMed ID: 27071392 [TBL] [Abstract][Full Text] [Related]
17. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene. Toto L; Boon CJ; Di Antonio L; Battaglia Parodi M; Mastropasqua R; Antonucci I; Stuppia L; Mastropasqua L Retina; 2016 Aug; 36(8):1586-95. PubMed ID: 26716959 [TBL] [Abstract][Full Text] [Related]
18. Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons. Wang Y; Jiang Y; Li X; Xiao X; Li S; Sun W; Wang P; Zhang Q Exp Eye Res; 2022 Oct; 223():109217. PubMed ID: 35973442 [TBL] [Abstract][Full Text] [Related]
19. A unique case series of autosomal recessive bestrophinopathy exhibiting multigenerational inheritance. Hardin JS; Schaefer GB; Sallam AB; Williams MK; Uwaydat S Ophthalmic Genet; 2017 Dec; 38(6):570-574. PubMed ID: 28481155 [TBL] [Abstract][Full Text] [Related]
20. Detection of Novel BEST1 Variations in Autosomal Recessive Bestrophinopathy Using Third-generation Sequencing. Li JX; Meng LR; Hou BK; Hao XL; Wang DJ; Qu LH; Li ZH; Zhang L; Jin X Curr Med Sci; 2024 Apr; 44(2):419-425. PubMed ID: 38619684 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]