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2. Multicolor Imaging Characteristics of Best's Vitelliform Macular Dystrophy. Saurabh K, Roy R, Thomas NR. Middle East Afr J Ophthalmol; 2019 Jul; 26(3):178-180. PubMed ID: 31619909 [Abstract] [Full Text] [Related]
3. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene. Eksandh L, Bakall B, Bauer B, Wadelius C, Andréasson S. Ophthalmic Genet; 2001 Jun; 22(2):107-15. PubMed ID: 11449320 [Abstract] [Full Text] [Related]
4. [Choroidal neovascularization complicating Best's vitelliform macular dystrophy in a child]. Elkhoyaali A, Chatoui S, Bercheq N, Elouatassi N, Zerrouk R, Elasri F, Reda K, Oubaaz A. J Fr Ophtalmol; 2016 Jan; 39(1):69-73. PubMed ID: 26707756 [Abstract] [Full Text] [Related]
5. Novel Presenting Phenotype in a Child With Autosomal Dominant Best's Vitelliform Macular Dystrophy. Abdalla YF, De Salvo G, Elsahn A, Self JE. Ophthalmic Surg Lasers Imaging Retina; 2017 Jul 01; 48(7):580-585. PubMed ID: 28728185 [Abstract] [Full Text] [Related]
6. Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysis. Meunier I, Sénéchal A, Dhaenens CM, Arndt C, Puech B, Defoort-Dhellemmes S, Manes G, Chazalette D, Mazoir E, Bocquet B, Hamel CP. Ophthalmology; 2011 Jun 01; 118(6):1130-6. PubMed ID: 21269699 [Abstract] [Full Text] [Related]
7. Various fundus manifestations in a Japanese family with Best's vitelliform macular dystrophy. Shibuya Y, Hayasaka S. Jpn J Ophthalmol; 1993 Jun 01; 37(4):478-84. PubMed ID: 8145393 [Abstract] [Full Text] [Related]
8. Electrooculography and optical coherence tomography reveal late-onset Best disease. Makati R, Shechtman D, Besada E, Pizzimenti JJ. Optom Vis Sci; 2014 Nov 01; 91(11):e274-7. PubMed ID: 25259760 [Abstract] [Full Text] [Related]
9. [Best's vitelliform macular dystrophy associated with choroidal neovascularization]. Céspedes A, Pérez-De-Arcelus M, García-Arumí J. Arch Soc Esp Oftalmol; 2012 Oct 01; 87(10):333-6. PubMed ID: 23021232 [Abstract] [Full Text] [Related]
10. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy. Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R. Ophthalmology; 2001 Nov 01; 108(11):2060-7. PubMed ID: 11713080 [Abstract] [Full Text] [Related]
11. Fundus autofluorescence imaging in Best's vitelliform dystrophy. Jarc-Vidmar M, Kraut A, Hawlina M. Klin Monbl Augenheilkd; 2003 Dec 01; 220(12):861-7. PubMed ID: 14704944 [Abstract] [Full Text] [Related]
12. Near-infrared fundus autofluorescence in subclinical best vitelliform macular dystrophy. Parodi MB, Iacono P, Del Turco C, Bandello F. Am J Ophthalmol; 2014 Dec 01; 158(6):1247-1252.e2. PubMed ID: 25174897 [Abstract] [Full Text] [Related]
13. Vitelliform lesions developing in normal fundi. Barricks ME. Am J Ophthalmol; 1977 Mar 01; 83(3):324-7. PubMed ID: 848535 [Abstract] [Full Text] [Related]
14. Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family. Hou YC, Richards JE, Bingham EL, Pawar H, Scott K, Segal M, Lunetta KL, Boehnke M, Sieving PA. Hum Hered; 1996 Mar 01; 46(4):211-20. PubMed ID: 8807324 [Abstract] [Full Text] [Related]
15. Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy. Matson ME, Ly SV, Monarrez JL. Optom Vis Sci; 2015 Aug 01; 92(8):e180-9. PubMed ID: 26099059 [Abstract] [Full Text] [Related]
16. Giant macular hole with Best's disease in a young boy. Mandal S, Basu S. Clin Exp Optom; 2012 Nov 01; 95(6):643-5. PubMed ID: 22725976 [Abstract] [Full Text] [Related]
17. [Best's disease with normal EOG. Case report of familial macular dystrophy]. Pollack K, Kreuz FR, Pillunat LE. Ophthalmologe; 2005 Sep 01; 102(9):891-4. PubMed ID: 15657694 [Abstract] [Full Text] [Related]
18. [Best's disease]. Roqai YC, Nawal K. Pan Afr Med J; 2019 Sep 01; 34():61. PubMed ID: 31762926 [Abstract] [Full Text] [Related]
20. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications. Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM. Arch Ophthalmol; 2011 Feb 01; 129(2):211-7. PubMed ID: 21320969 [Abstract] [Full Text] [Related] Page: [Next] [New Search]