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Journal Abstract Search
377 related items for PubMed ID: 15671300
1. Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and loci. Umeda S, Ayyagari R, Allikmets R, Suzuki MT, Karoukis AJ, Ambasudhan R, Zernant J, Okamoto H, Ono F, Terao K, Mizota A, Yoshikawa Y, Tanaka Y, Iwata T. Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):683-91. PubMed ID: 15671300 [Abstract] [Full Text] [Related]
9. Late-onset autosomal dominant macular dystrophy with choroidal neovascularization and nonexudative maculopathy associated with mutation in the RDS gene. Khani SC, Karoukis AJ, Young JE, Ambasudhan R, Burch T, Stockton R, Lewis RA, Sullivan LS, Daiger SP, Reichel E, Ayyagari R. Invest Ophthalmol Vis Sci; 2003 Aug; 44(8):3570-7. PubMed ID: 12882809 [Abstract] [Full Text] [Related]
10. 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]
13. Identification of a novel VMD2 mutation in Japanese patients with Best disease. Yanagi Y, Sekine H, Mori M. Ophthalmic Genet; 2002 Jun; 23(2):129-33. PubMed ID: 12187431 [Abstract] [Full Text] [Related]
14. Benign Yellow Dot Maculopathy: A New Macular Phenotype. Dev Borman A, Rachitskaya A, Suzani M, Sisk RA, Ahmed ZM, Holder GE, Cipriani V, Arno G, Webster AR, Hufnagel RB, Berrocal A, Moore AT. Ophthalmology; 2017 Jul; 124(7):1004-1013. PubMed ID: 28366503 [Abstract] [Full Text] [Related]