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791 related items for PubMed ID: 28187978
1. Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy. Qian CX, Charran D, Strong CR, Steffens TJ, Jayasundera T, Heckenlively JR. Ophthalmology; 2017 Apr; 124(4):456-463. PubMed ID: 28187978 [Abstract] [Full Text] [Related]
2. Three-dimensional distribution of the vitelliform lesion, photoreceptors, and retinal pigment epithelium in the macula of patients with best vitelliform macular dystrophy. Kay CN, Abramoff MD, Mullins RF, Kinnick TR, Lee K, Eyestone ME, Chung MM, Sohn EH, Stone EM. Arch Ophthalmol; 2012 Mar; 130(3):357-64. PubMed ID: 22084158 [Abstract] [Full Text] [Related]
9. IMAGING OF VITELLIFORM MACULAR LESIONS USING POLARIZATION-SENSITIVE OPTICAL COHERENCE TOMOGRAPHY. Deák GG, Schmidt WM, Bittner RE, Mylonas G, Roberts PK, Zotter S, Baumann B, Pircher M, Hitzenberger CK, Schmidt-Erfurth UM, Ritter M. Retina; 2019 Mar; 39(3):558-569. PubMed ID: 29215532 [Abstract] [Full Text] [Related]
10. Multimodal imaging in Best Vitelliform Macular Dystrophy: Literature review and novel insights. Bianco L, Arrigo A, Antropoli A, Berni A, Saladino A, Vilela MA, Mansour AM, Bandello F, Battaglia Parodi M. Eur J Ophthalmol; 2024 Jan; 34(1):39-51. PubMed ID: 36972471 [Abstract] [Full Text] [Related]
11. Optical coherence tomography in Best vitelliform macular dystrophy. Battaglia Parodi M, Iacono P, Romano F, Bolognesi G, Fasce F, Bandello F. Eur J Ophthalmol; 2017 Mar 10; 27(2):201-204. PubMed ID: 28233888 [Abstract] [Full Text] [Related]
12. Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes. Meunier I, Manes G, Bocquet B, Marquette V, Baudoin C, Puech B, Defoort-Dhellemmes S, Audo I, Verdet R, Arndt C, Zanlonghi X, Le Meur G, Dhaenens CM, Hamel CP. Ophthalmology; 2014 Dec 10; 121(12):2406-14. PubMed ID: 25085631 [Abstract] [Full Text] [Related]
14. Quantitative Fundus Autofluorescence in Best Vitelliform Macular Dystrophy: RPE Lipofuscin is not Increased in Non-Lesion Areas of Retina. Sparrow JR, Duncker T, Woods R, Delori FC. Adv Exp Med Biol; 2016 Dec 10; 854():285-90. PubMed ID: 26427423 [Abstract] [Full Text] [Related]
17. Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy. Lacassagne E, Dhuez A, Rigaudière F, Dansault A, Vêtu C, Bigot K, Vieira V, Puech B, Defoort-Dhellemmes S, Abitbol M. Mol Vis; 2011 Jan 29; 17():309-22. PubMed ID: 21293734 [Abstract] [Full Text] [Related]
18. Bilateral macular holes and a new onset vitelliform lesion in Best disease. Liu J, Xuan Y, Zhang Y, Liu W, Xu G. Ophthalmic Genet; 2017 Jan 29; 38(1):79-82. PubMed ID: 27031371 [Abstract] [Full Text] [Related]
19. Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy. Matson ME, Ly SV, Monarrez JL. Optom Vis Sci; 2015 Aug 29; 92(8):e180-9. PubMed ID: 26099059 [Abstract] [Full Text] [Related]
20. Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy. Schatz P, Sharon D, Al-Hamdani S, Andréasson S, Larsen M. Graefes Arch Clin Exp Ophthalmol; 2016 Feb 29; 254(2):215-21. PubMed ID: 25940553 [Abstract] [Full Text] [Related] Page: [Next] [New Search]