Ophthalmology, Third Edition: Expert Consult: Online and by Myron Yanoff MD

By Myron Yanoff MD

In keeping with invaluable shopper suggestions, medical professionals Yanoff and Duker have streamlined their best-selling reference, Ophthalmology, to 0 in on simply the medical solutions you would like in daily perform. they have got rid of many of the uncomplicated technological know-how and anatomy details from the published ebook and positioned it at the better half site the place it's simply obtainable in addition to the total contents of the e-book. This new version offers unheard of suggestions on approximately each ophthalmic and process together with the most recent advances within the box, comparable to optical coherence tomography (OCT), the ocular floor, new pharmacologic treatments, up to date oculoplastic surgical thoughts, the newest in refractive surgical procedure, and much more. And, as a professional seek advice identify, this meticulously up to date third version comes with entry to the entire contents on-line, absolutely searchable, plus extra simple technology information.Provides entry to the full contents on-line, totally searchable, plus extra easy technology details, and a downloadable photograph library to be used in digital shows. Discusses each point of scientific ophthalmology for entire insurance in one quantity. makes use of 2250 full-color illustrations that depict a variety of ophthalmic ideas and disorders.Presents a extra streamlined structure to the broadcast textual content that will help you specialize in the clinically actionable details you wish everyday.Discusses sizzling subject matters such OCT, the ocular floor, glaucoma trying out, refractive surgical procedure, advances in molecular biology and genetics, neuro-ophthalmology, and retinal stories to maintain you totally present. offers greater assurance of cataracts, together with advances in phacoemulsification and surgical complications.Helps you're making optimum use of the latest drug remedies, together with Anti-VEGF therapy for rainy ARMD and bevacizumab therapy for issues of diabetes. deals authoritative counsel at the most recent treatments for cornea problems, together with evolving ocular floor reconstruction concepts and new cornea approaches corresponding to DSEK.Incorporates new chapters on more and more well known aesthetic oculoplastic surgical thoughts that will help you meet brand new demands.Your buy entitles you to entry the website until eventually the following variation is released, or until eventually the present version isn't any longer provided on the market through Elsevier, whichever happens first. If the following variation is released below 12 months after your buy, you can be entitled to on-line entry for twelve months out of your date of buy. Elsevier reserves the best to supply an appropriate substitute product (such as a downloadable or CD-ROM-based digital model) should still entry to the website be discontinued.

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Science. 2005;308:421–4. Haines JL, Hauser MA, Schmidt S, et al. Complement factor H variant increases the risk of age-related macular degeneration. Science. 2005;308:419–21. Rivera A, Fisher SA, Fritsche LG, et al. Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing ­independently of complement factor H to disease risk. Hum Mol Genet. 2005;14:3227–36. Schmidt S, Hauser MA, Scott WK, et al. Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.

Nat Genet. 2001;29:315–20. Al-Baradie R, Yamada K, St Hilaire C, et al. Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL ­family. Am J Hum Genet . 2002;71:1195–9. Votruba M, Moore AT, Bhattacharya SS. Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q. J Med Genet. 1997;34:117–21. Alexander C, Votruba M, Pesch UE, et al. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.

2004;48:1015–29. Libby RT, Smith RS, Savinova OV, et al. Modification of ocular defects in mouse developmental glaucoma models by tyrosinase. Science. 2003;299:1578–81. Bejjani BA, Stockton DW, Lewis RA, et al. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet. 2000;9:367–74. Bidinost C, Hernandez N, Edward DP, et al. Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humans.

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