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

By Myron Yanoff MD

In line with useful buyer 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 day by day perform. they have got rid of lots of the easy technology and anatomy info from the published publication and placed it at the better half site the place it's simply available besides the full contents of the publication. This re-creation offers exceptional assistance on approximately each ophthalmic situation and process together with the most recent advances within the box, equivalent to optical coherence tomography (OCT), the ocular floor, new pharmacologic cures, up-to-date oculoplastic surgical strategies, the newest in refractive surgical procedure, and a lot more. And, as knowledgeable seek advice name, this meticulously up-to-date third variation comes with entry to the entire contents on-line, totally searchable, plus extra uncomplicated technological know-how information.Provides entry to the full contents on-line, absolutely searchable, plus extra uncomplicated technology details, and a downloadable picture library to be used in digital displays. Discusses each point of medical ophthalmology for whole assurance in one quantity. makes use of 2250 full-color illustrations that depict a variety of ophthalmic ideas and disorders.Presents a extra streamlined layout to the broadcast textual content that will help you concentrate on the clinically actionable details you wish everyday.Discusses sizzling themes such OCT, the ocular floor, glaucoma checking out, refractive surgical procedure, advances in molecular biology and genetics, neuro-ophthalmology, and retinal reviews to maintain you totally present. presents greater insurance of cataracts, together with advances in phacoemulsification and surgical complications.Helps you're making optimum use of the latest drug cures, together with Anti-VEGF therapy for rainy ARMD and bevacizumab remedy for issues of diabetes. deals authoritative suggestions at the most modern cures for cornea problems, together with evolving ocular floor reconstruction concepts and new cornea strategies resembling DSEK.Incorporates new chapters on more and more well known aesthetic oculoplastic surgical suggestions that will help you meet modern day demands.Your buy entitles you to entry the website until eventually the subsequent variation is released, or till the present version is not any longer provided on the market through Elsevier, whichever happens first. If the following version is released below twelve months after your buy, you can be entitled to on-line entry for 365 days out of your date of buy. Elsevier reserves the precise to supply an appropriate substitute product (such as a downloadable or CD-ROM-based digital model) may still entry to the website be discontinued.

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Ott J. Analysis of human genetic linkage. 2nd ed. Baltimore: Johns Hopkins University Press; 1991. MacDonald IM, Sereda C, McTaggart K, Mah D. Choroideremia gene testing. Expert Rev Mol Diagn 2004;4:478–84. Review. Mulot C, Stucker I, Clavel J, et al. Collection of human genomic DNA from buccal cells for genetics studies: comparison between cytobrush, mouthwash, and treated card. J Biomed Biotechnol 2005;3:291–6. Onadim Z, Cowell JK. Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.

However, inactivation of the remaining normal copy of the retinoblastoma gene is very likely in at least one retinal cell out of the millions present in each retina. Among individuals who inherit a mutant copy of the retinoblastoma gene, 90% sustain a second hit to the remaining normal copy of the gene and develop a tumor (Fig. 103 Fifty per cent of the offspring of individuals affected by hereditary retinoblastoma inherit the mutant copy of the gene and are predisposed to develop the tumor. Approximately 10% of individuals who inherit a mutant copy of the gene do not sustain a second mutation and do not develop a tumor.

1997;16:184–7. Corden LD, Swensson O, Swensson B, et al. Molecular genetics of Meesmann’s corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene. Exp Eye Res. 2000;70:41–9. Glaser T, Jepeal L, Edwards JG, et al. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nat Genet. 1994;7:463–71. Hanson IM, Fletcher JM, Jordon T, et al. Mutations at the PAX6 locus are found in heterogeneous anterior ­segment malformations including Peters’ anomaly.

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