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 *

167 related articles for article (PubMed ID: 21892605)

  • 1. The characterization of functional disturbances in Chinese patients with Bietti's crystalline dystrophy at different fundus stages.
    Liu DN; Liu Y; Meng XH; Yin ZQ
    Graefes Arch Clin Exp Ophthalmol; 2012 Feb; 250(2):191-200. PubMed ID: 21892605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bietti's crystalline dystrophy: genotyping and deep qualitative and quantitative phenotyping in preparation for clinical trials.
    Li Q; Wang C; Zhang S; Fu Z; Jiao X; Jin ZB; Hejtmancik JF; Peng X
    Br J Ophthalmol; 2024 Jul; 108(8):1145-1153. PubMed ID: 37963713
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bietti's crystalline dystrophy in Asians: clinical, angiographic and electrophysiological characteristics.
    Fong AM; Koh A; Lee K; Ang CL
    Int Ophthalmol; 2009 Dec; 29(6):459-70. PubMed ID: 18854949
    [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. Multimodal imaging of Bietti's crystalline dystrophy.
    Kumar V; Gadkar A
    Indian J Ophthalmol; 2018 Jul; 66(7):1024-1026. PubMed ID: 29941763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Evaluation of Photoreceptors in Bietti Crystalline Dystrophy with CYP4V2 Mutations Using Adaptive Optics Scanning Laser Ophthalmoscopy.
    Miyata M; Ooto S; Ogino K; Gotoh N; Morooka S; Makiyama Y; Hasegawa T; Sugahara M; Hata M; Yamashiro K; Yoshimura N
    Am J Ophthalmol; 2016 Jan; 161():196-205.e1. PubMed ID: 26521715
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Novel CYP4V2 gene mutation in a Mexican patient with Bietti's crystalline corneoretinal dystrophy.
    Zenteno JC; Ayala-Ramirez R; Graue-Wiechers F
    Curr Eye Res; 2008 Apr; 33(4):313-8. PubMed ID: 18398705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti's crystalline dystrophy.
    Song Y; Mo G; Yin G
    Int Ophthalmol; 2013 Jun; 33(3):269-76. PubMed ID: 23242590
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy.
    Wada Y; Itabashi T; Sato H; Kawamura M; Tada A; Tamai M
    Am J Ophthalmol; 2005 May; 139(5):894-9. PubMed ID: 15860296
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti's crystalline corneoretinal dystrophy.
    Meng XH; Guo H; Xu HW; Li QY; Jin X; Bai Y; Li SY; Yin ZQ
    Mol Vis; 2014; 20():1806-14. PubMed ID: 25593508
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. DISCREPANCY BETWEEN FUNDUS AUTOFLUORESCENCE ABNORMALITY AND VISUAL FIELD LOSS IN BIETTI CRYSTALLINE DYSTROPHY.
    Sakai D; Maeda T; Maeda A; Yamamoto M; Yokota S; Hirami Y; Nakamura M; Takahashi M; Mandai M; Kurimoto Y
    Retina; 2024 Aug; 44(8):1394-1402. PubMed ID: 39047130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Bietti's crystalline dystrophy in Nepalese patients: when genetic analysis supports clinical diagnosis.
    Suwal B; Bajimaya S; Bernstein PS
    Ophthalmic Genet; 2019 Aug; 40(4):390-392. PubMed ID: 31512983
    [No Abstract]   [Full Text] [Related]  

  • 19. Genotype phenotype analysis of Bietti's crystalline dystrophy in patients with CYP4V2 mutations.
    Lai TY; Ng TK; Tam PO; Yam GH; Ngai JW; Chan WM; Liu DT; Lam DS; Pang CP
    Invest Ophthalmol Vis Sci; 2007 Nov; 48(11):5212-20. PubMed ID: 17962476
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.