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Journal Abstract Search

127 related items for PubMed ID: 29234872

  • 1. [Multimodal imaging in Goldmann-Favre syndrome].
    Valler D, Ulbig M, Lohmann CP, Maier M.
    Ophthalmologe; 2018 Oct; 115(10):878-882. PubMed ID: 29234872
    [Abstract] [Full Text] [Related]

  • 2. Bilateral giant macular schisis in a case of Goldmann-Favre syndrome.
    Chawla R, Banerjee M.
    BMJ Case Rep; 2019 Sep 26; 12(9):. PubMed ID: 31558488
    [Abstract] [Full Text] [Related]

  • 3. Goldmann-Favre vitreoretinal degeneration.
    Batioğlu F.
    Eur J Ophthalmol; 2003 Apr 26; 13(3):307-10. PubMed ID: 12747653
    [Abstract] [Full Text] [Related]

  • 4. En Face Optical Coherence Tomography Imaging in Enhanced S-Cone Syndrome.
    Ortoli M, Zambrowski O, Miere A, Gerber S, Kaplan J, Souied E.
    Retina; 2020 Aug 26; 40(8):e32-e33. PubMed ID: 32467484
    [No Abstract] [Full Text] [Related]

  • 5. Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report.
    Minnella AM, Pagliei V, Savastano MC, Federici M, Bertelli M, Maltese PE, Placidi G, Corbo G, Falsini B, Caporossi A.
    J Med Case Rep; 2018 Oct 03; 12(1):287. PubMed ID: 30285900
    [Abstract] [Full Text] [Related]

  • 6. Clinical features of Goldmann-Favre syndrome.
    Ikäheimo K, Tuppurainen K, Mäntyjärvi M.
    Acta Ophthalmol Scand; 1999 Aug 03; 77(4):459-61. PubMed ID: 10463423
    [Abstract] [Full Text] [Related]

  • 7. New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.
    Kuniyoshi K, Hayashi T, Sakuramoto H, Mishima H, Tsuneoka H, Tsunoda K, Iwata T, Shimomura Y.
    Jpn J Ophthalmol; 2016 Nov 03; 60(6):476-485. PubMed ID: 27522502
    [Abstract] [Full Text] [Related]

  • 8. Goldmann-Favre syndrome in a four-year-old-girl.
    Izumi K, Matsuhashi M.
    Doc Ophthalmol; 1987 Jun 03; 66(3):219-26. PubMed ID: 3428076
    [Abstract] [Full Text] [Related]

  • 9. Pigmented Paravenous Chorioretinal Atrophy: Clinical Spectrum and Multimodal Imaging Characteristics.
    Lee EK, Lee SY, Oh BL, Yoon CK, Park UC, Yu HG.
    Am J Ophthalmol; 2021 Apr 03; 224():120-132. PubMed ID: 33340506
    [Abstract] [Full Text] [Related]

  • 10. 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 03; 120(4):809-20. PubMed ID: 23290749
    [Abstract] [Full Text] [Related]

  • 11. A novel mutation in the NR2E3 gene associated with Goldmann-Favre syndrome and vasoproliferative tumor of the retina.
    Manayath GJ, Namburi P, Periasamy S, Kale JA, Narendran V, Ganesh A.
    Mol Vis; 2014 Apr 03; 20():724-31. PubMed ID: 24891813
    [Abstract] [Full Text] [Related]

  • 12. Novel findings in enhanced S-cone syndrome: a case with macular retinal neovascularization and severe retinal vasculitis.
    Bazvand F, Khojasteh H, Zarei M.
    Doc Ophthalmol; 2019 Dec 03; 139(3):221-226. PubMed ID: 31292819
    [Abstract] [Full Text] [Related]

  • 13. Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.
    Scheidecker S, Hull S, Perdomo Y, Studer F, Pelletier V, Muller J, Stoetzel C, Schaefer E, Defoort-Dhellemmes S, Drumare I, Holder GE, Hamel CP, Webster AR, Moore AT, Puech B, Dollfus HJ.
    Am J Ophthalmol; 2015 Aug 03; 160(2):364-372.e1. PubMed ID: 25982971
    [Abstract] [Full Text] [Related]

  • 14. Recognizable Patterns of Submacular Fibrosis in Enhanced S-Cone Syndrome.
    Alsalamah AK, Khan AO, Bakar AA, Schatz P, Nowilaty SR.
    Ophthalmol Retina; 2021 Sep 03; 5(9):918-927. PubMed ID: 33819700
    [Abstract] [Full Text] [Related]

  • 15. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
    Sustar M, Perovšek D, Cima I, Stirn-Kranjc B, Hawlina M, Brecelj J.
    Doc Ophthalmol; 2015 Jun 03; 130(3):165-77. PubMed ID: 25663266
    [Abstract] [Full Text] [Related]

  • 16. MULTIMODAL EVIDENCE OF TYPE 3 NEOVASCULARIZATION IN ENHANCED S-CONE SYNDROME.
    Maldonado RS, Zein WM, Cukras C.
    Retin Cases Brief Rep; 2021 Nov 01; 15(6):702-708. PubMed ID: 31356371
    [Abstract] [Full Text] [Related]

  • 17. Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.
    Kellner S, Stöhr H, Fiebig B, Weinitz S, Farmand G, Kellner U, Weber BH.
    Ophthalmic Genet; 2016 Jun 01; 37(2):201-8. PubMed ID: 26771239
    [Abstract] [Full Text] [Related]

  • 18. Macular dystrophy associated with Kjellin's syndrome: a case report.
    Castro VM, Meirelles A, Arcieri RS, Messias K, Messias A.
    Arq Bras Oftalmol; 2015 Jun 01; 78(2):120-2. PubMed ID: 25945536
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.
    de Laat P, Smeitink JAM, Janssen MCH, Keunen JEE, Boon CJF.
    Ophthalmology; 2013 Dec 01; 120(12):2684-2696. PubMed ID: 23806424
    [Abstract] [Full Text] [Related]

  • 20. Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome).
    Tsang SH, Sharma T.
    Adv Exp Med Biol; 2018 Dec 01; 1085():153-156. PubMed ID: 30578501
    [Abstract] [Full Text] [Related]

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