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Journal Abstract Search

191 related items for PubMed ID: 28487376

  • 1. Visual and ocular motor function in the atypical form of neurodegeneration with brain iron accumulation type I.
    Jesus-Ribeiro J, Farinha C, Amorim M, Matos A, Reis A, Lemos J, Castelo-Branco M, Januário C.
    Br J Ophthalmol; 2018 Jan; 102(1):102-108. PubMed ID: 28487376
    [Abstract] [Full Text] [Related]

  • 2. Electrophysiological assessment for early detection of retinal dysfunction in β-thalassemia major patients.
    Dettoraki M, Kattamis A, Ladas I, Maragkos K, Koutsandrea C, Chatzistefanou K, Laios K, Brouzas D, Moschos MM.
    Graefes Arch Clin Exp Ophthalmol; 2017 Jul; 255(7):1349-1358. PubMed ID: 28361176
    [Abstract] [Full Text] [Related]

  • 3. Retinal and optic nerve abnormalities in neurodegeneration associated with mutations in C19orf12 (MPAN).
    Langwinska-Wosko E, Skowronska M, Kmiec T, Czlonkowska A.
    J Neurol Sci; 2016 Nov 15; 370():237-240. PubMed ID: 27772766
    [Abstract] [Full Text] [Related]

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  • 5. Diabetic macular edema: fundus autofluorescence and functional correlations.
    Vujosevic S, Casciano M, Pilotto E, Boccassini B, Varano M, Midena E.
    Invest Ophthalmol Vis Sci; 2011 Jan 21; 52(1):442-8. PubMed ID: 20720226
    [Abstract] [Full Text] [Related]

  • 6. Vascular abnormalities in patients with Stargardt disease assessed with optical coherence tomography angiography.
    Battaglia Parodi M, Cicinelli MV, Rabiolo A, Pierro L, Bolognesi G, Bandello F.
    Br J Ophthalmol; 2017 Jun 21; 101(6):780-785. PubMed ID: 27628426
    [Abstract] [Full Text] [Related]

  • 7. Multimodal imaging of foveal cavitation in retinal dystrophies.
    Parodi MB, Cicinelli MV, Iacono P, Bolognesi G, Bandello F.
    Graefes Arch Clin Exp Ophthalmol; 2017 Feb 21; 255(2):271-279. PubMed ID: 27491512
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  • 8. Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report.
    Salvucci IDM, Finzi S, Oyamada MK, Kim CA, Pimentel SLG.
    Ophthalmic Genet; 2018 Feb 21; 39(1):103-107. PubMed ID: 28820625
    [Abstract] [Full Text] [Related]

  • 9. Fundus autofluorescence and optical coherence tomography findings in glutathione synthetase deficiency.
    Şekeroğlu HT, Hismi B, Kadayifcilar S, Coskun T.
    J AAPOS; 2015 Feb 21; 19(1):80-2. PubMed ID: 25727596
    [Abstract] [Full Text] [Related]

  • 10. Diagnostic fundus autofluorescence patterns in achromatopsia.
    Fahim AT, Khan NW, Zahid S, Schachar IH, Branham K, Kohl S, Wissinger B, Elner VM, Heckenlively JR, Jayasundera T.
    Am J Ophthalmol; 2013 Dec 21; 156(6):1211-1219.e2. PubMed ID: 23972307
    [Abstract] [Full Text] [Related]

  • 11. Microperimetric assessment of the two optical coherence tomography subtypes of acute macular neuroretinopathy.
    Battaglia Parodi M, Iacono P, Panico D, Cascavilla M, Bandello F.
    Clin Exp Ophthalmol; 2015 Dec 21; 43(7):637-42. PubMed ID: 25752249
    [Abstract] [Full Text] [Related]

  • 12. Early-onset stargardt disease: phenotypic and genotypic characteristics.
    Lambertus S, van Huet RA, Bax NM, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB.
    Ophthalmology; 2015 Feb 21; 122(2):335-44. PubMed ID: 25444351
    [Abstract] [Full Text] [Related]

  • 13. Cobalt-Chromium Metallosis With Normal Electroretinogram.
    Grillo LM, Nguyen HV, Tsang SH, Hood DC, Odel JG.
    J Neuroophthalmol; 2016 Dec 21; 36(4):383-388. PubMed ID: 27295601
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  • 15. Ocular manifestations of cobalamin C type methylmalonic aciduria with homocystinuria.
    Fuchs LR, Robert M, Ingster-Moati I, Couette L, Dufier JL, de Lonlay P, Brodie SE.
    J AAPOS; 2012 Aug 21; 16(4):370-5. PubMed ID: 22929452
    [Abstract] [Full Text] [Related]

  • 16. The Ocular Phenotype in Primary Hyperoxaluria Type 1.
    Birtel J, Herrmann P, Garrelfs SF, Dulz S, Atiskova Y, Diederen RM, Gliem M, Brinkert F, Holz FG, Boon CJF, Hoppe B, Charbel Issa P.
    Am J Ophthalmol; 2019 Oct 21; 206():184-191. PubMed ID: 31078535
    [Abstract] [Full Text] [Related]

  • 17. [Radial optic neurotomy for ischemic central retinal vein occlusion].
    Lommatzsch A, Heimes B, Gutfleisch M, Spital G, Trieschmann M, Pauleikhoff D.
    Klin Monbl Augenheilkd; 2007 Oct 21; 224(10):763-9. PubMed ID: 17952819
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  • 19. 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 01; 61(11):27. PubMed ID: 32931575
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