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155 results
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Integrity of the cone photoreceptor mosaic in oligocone trichromacy.
Michaelides M, Rha J, Dees EW, Baraas RC, Wagner-Schuman ML, Mollon JD, Dubis AM, Andersen MK, Rosenberg T, Larsen M, Moore AT, Carroll J. Michaelides M, et al. Among authors: mollon jd. Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4757-64. doi: 10.1167/iovs.10-6659. Invest Ophthalmol Vis Sci. 2011. PMID: 21436275 Free PMC article.
Progressive cone dystrophy associated with mutation in CNGB3.
Michaelides M, Aligianis IA, Ainsworth JR, Good P, Mollon JD, Maher ER, Moore AT, Hunt DM. Michaelides M, et al. Among authors: mollon jd. Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1975-82. doi: 10.1167/iovs.03-0898. Invest Ophthalmol Vis Sci. 2004. PMID: 15161866
X-linked cone dysfunction syndrome with myopia and protanopia.
Michaelides M, Johnson S, Bradshaw K, Holder GE, Simunovic MP, Mollon JD, Moore AT, Hunt DM. Michaelides M, et al. Among authors: mollon jd. Ophthalmology. 2005 Aug;112(8):1448-54. doi: 10.1016/j.ophtha.2005.02.021. Ophthalmology. 2005. PMID: 15953640
The chemistry of John Dalton's color blindness.
Hunt DM, Dulai KS, Bowmaker JK, Mollon JD. Hunt DM, et al. Among authors: mollon jd. Science. 1995 Feb 17;267(5200):984-8. doi: 10.1126/science.7863342. Science. 1995. PMID: 7863342
Achromatopsia caused by novel mutations in both CNGA3 and CNGB3.
Johnson S, Michaelides M, Aligianis IA, Ainsworth JR, Mollon JD, Maher ER, Moore AT, Hunt DM. Johnson S, et al. Among authors: mollon jd. J Med Genet. 2004 Feb;41(2):e20. doi: 10.1136/jmg.2003.011437. J Med Genet. 2004. PMID: 14757870 Free PMC article. No abstract available.
155 results