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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

254 related articles for article (PubMed ID: 32799831)

  • 1. Multimodal imaging features and genetic findings in Bietti crystalline dystrophy.
    Wang W; Chen W; Bai X; Chen L
    BMC Ophthalmol; 2020 Aug; 20(1):331. PubMed ID: 32799831
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization.
    Fuerst NM; Serrano L; Han G; Morgan JI; Maguire AM; Leroy BP; Kim BJ; Aleman TS
    Ophthalmic Genet; 2016 Dec; 37(4):445-452. PubMed ID: 27028354
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation of
    Han XY; Zhang LQ; Tang JY; Huang LZ; Tang R; Qu JF
    Int J Ophthalmol; 2022; 15(6):940-946. PubMed ID: 35814885
    [TBL] [Abstract][Full Text] [Related]  

  • 4. UTILIZATION OF FUNDUS AUTOFLUORESCENCE, SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY, AND ENHANCED DEPTH IMAGING IN THE CHARACTERIZATION OF BIETTI CRYSTALLINE DYSTROPHY IN DIFFERENT STAGES.
    Li Q; Li Y; Zhang X; Xu Z; Zhu X; Ma K; She H; Peng X
    Retina; 2015 Oct; 35(10):2074-84. PubMed ID: 25978730
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Optical coherence tomography and optical coherence tomography angiography imaging in Bietti crystalline dystrophy.
    Tiryaki Demir S; Keles Yesiltas S; Kacar H; Akbas EB; Guven D
    Ophthalmic Genet; 2020 Apr; 41(2):194-197. PubMed ID: 32281452
    [No Abstract]   [Full Text] [Related]  

  • 6. Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in
    Lockhart CM; Smith TB; Yang P; Naidu M; Rettie AE; Nath A; Weleber R; Kelly EJ
    Br J Ophthalmol; 2018 Feb; 102(2):187-194. PubMed ID: 28698241
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy.
    Halford S; Liew G; Mackay DS; Sergouniotis PI; Holt R; Broadgate S; Volpi EV; Ocaka L; Robson AG; Holder GE; Moore AT; Michaelides M; Webster AR
    Ophthalmology; 2014 Jun; 121(6):1174-84. PubMed ID: 24480711
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CHOROIDAL AND RETINAL ATROPHY OF BIETTI CRYSTALLINE DYSTROPHY PATIENTS WITH CYP4V2 MUTATIONS COMPARED TO RETINITIS PIGMENTOSA PATIENTS WITH EYS MUTATIONS.
    Miyata M; Hata M; Ooto S; Ogino K; Gotoh N; Morooka S; Hasegawa T; Hirashima T; Sugahara M; Kuroda Y; Yamashiro K; Yoshimura N
    Retina; 2017 Jun; 37(6):1193-1202. PubMed ID: 27658286
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Choroidal Vasculature in Bietti Crystalline Dystrophy With CYP4V2 Mutations and in Retinitis Pigmentosa With EYS Mutations.
    Hirashima T; Miyata M; Ishihara K; Hasegawa T; Sugahara M; Ogino K; Yoshikawa M; Hata M; Kuroda Y; Muraoka Y; Ooto S; Yoshimura N
    Invest Ophthalmol Vis Sci; 2017 Aug; 58(10):3871-3878. PubMed ID: 28763560
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 2021 Dec; 5(12):1269-1279. PubMed ID: 33636399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype and Ocular Phenotype in Sixteen Chinese Patients with Bietti Corneoretinal Crystalline Dystrophy.
    Dai H; Zhang Y; Li R; Li Y; Li G
    Curr Eye Res; 2022 Mar; 47(3):436-442. PubMed ID: 34724870
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy.
    Yin X; Yang L; Chen N; Cui H; Zhao L; Feng L; Li A; Zhang H; Ma Z; Li G
    Exp Eye Res; 2016 May; 146():154-162. PubMed ID: 26971461
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: report on a novel mutation.
    Haddad NM; Waked N; Bejjani R; Khoueir Z; Chouery E; Corbani S; Mégarbané A
    Mol Vis; 2012; 18():1182-8. PubMed ID: 22605929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetics of Bietti Crystalline Dystrophy.
    Ng DS; Lai TY; Ng TK; Pang CP
    Asia Pac J Ophthalmol (Phila); 2016; 5(4):245-52. PubMed ID: 27228076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An atypical form of Bietti crystalline dystrophy.
    Rossi S; Testa F; Li A; Iorio VD; Zhang J; Gesualdo C; Corte MD; Chan CC; Fielding Hejtmancik J; Simonelli F
    Ophthalmic Genet; 2011 Jun; 32(2):118-21. PubMed ID: 21385027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structural and functional phenotypic features and molecular analysis of Indian patients with Bietti crystalline dystrophy.
    Ratra D; Chattree S; Raviselvan M; Pradhan A; Giridhar S
    Indian J Ophthalmol; 2022 Jul; 70(7):2526-2532. PubMed ID: 35791149
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization.
    Mamatha G; Umashankar V; Kasinathan N; Krishnan T; Sathyabaarathi R; Karthiyayini T; Amali J; Rao C; Madhavan J
    Mol Vis; 2011; 17():1970-7. PubMed ID: 21850171
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and genetic features in Italian Bietti crystalline dystrophy patients.
    Br J Ophthalmol; ; . PubMed ID: 23221965
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.