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Ocular disease mechanisms and management [edited by] Leonard Levin, Daniel Albert.

Colaborador(es): Detalles de publicación: St. Louis,Minnesota Saunders;Elsevier c2010.Descripción: xv,687p. ill. 28 cmISBN:
  • 9780702029837
Tema(s): Clasificación LoC:
  • RE 46 .O29 2010
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Ocular Disease-a newly introduced companion volume to the classic Adler's Physiology of the Eye-correlates basic science and clinical management to describe the how and why of eye disease processes and the related best management protocols. Editors Leonard A. Levin and Daniel M. Albert-two of the world's leading ophthalmic clinician-scientists-have recruited as contributors the most expert and experienced authorities available in each of the major areas of ophthalmic disease specific to ophthalmology: retina, cornea, cataract, glaucoma, uveitis, and more. The concise chapter structure features liberal use of color-with 330 full-color line artworks, call-out boxes, summaries, and schematics for easy navigation and understanding. In print and online at expertconsult.com, this comprehensive resource provides you with a better and more practical understanding of the science behind eye disease and its relation to treatment.

Includes access to the fully searchable text online at expertconsult.com, along with images and references. Covers all areas of disease in ophthalmology including retina, cornea, cataract, glaucoma, and uveitis for the comprehensive information you need for managing clinical cases. Presents a unique and pragmatic blend of necessary basic science and clinical application to serve as a clinical guide to understanding the cause and rational management of ocular disease. Features 330 full-color line artworks that translate difficult concepts and discussions into concise schematics for improved understanding and comprehension. Provides the expert advice of internationally recognized editors with over 40 years of experience together with a group of world class contributors in basic science and clinical ophthalmology.

Includes bibliographical references and index.

EIGM 03/2010

Tabla de contenidos provista por Syndetics

  • Section 1 Cornea
  • 1 Loss of corneal transparency
  • 2 Abnormalities of corneal wound healing
  • 3 Wound healing after laser in situ keratomileusis and photorefractive keratectomy
  • 4 Genetics and mechanisms of hereditary corneal dystrophies
  • 5 Fuchs' endothelial corneal dystrophy
  • 6 Keratoconus
  • 7 Infectious keratitis
  • 8 Corneal graft rejection
  • 9 Corneal edema
  • 10 Corneal angiogenesis and lymphangiogenesis
  • 11 Ocular surface restoration
  • 12 Herpetic keratitis
  • 13 Ocular allergy
  • Section 2 Dry eye
  • 14 The lacrimal gland and dry-eye disease
  • 15 Immune mechanisms of dry-eye disease
  • 16 Disruption of tear film and blink dynamics
  • 17 Abnormalities of eyelid and tear film lipid
  • 18 Dry eye: abnormalities of tear film mucins
  • Section 3 Glaucoma
  • 19 Steroid-induced glaucoma
  • 20 Biomechanical changes of the optic disc
  • 21 Pigmentary dispersion syndrome and glaucoma
  • 22 Abnormal trabecular meshwork outflow
  • 23 Pressure-induced optic nerve damage
  • 24 Exfoliation (pseudoexfoliation) syndrome
  • 25 Angle closure glaucoma
  • 26 Central nervous system changes in glaucoma
  • 27 Retinal ganglion cell death in glaucoma
  • 28 Wound-healing responses to glaucoma surgery
  • 29 Blood flowchanges in glaucoma
  • Section 4 Lens
  • 30 Biochemical mechanisms of age-related cataract
  • 31 Posterior capsule opacification
  • 32 Diabetes-associated cataracts
  • 33 Steroid-induced cataract
  • 34 Presbyopia
  • 35 Restoration of accommodation
  • 36 Intraoperative floppy iris syndrome
  • Section 5 Neuro-ophthalmology
  • 37 Optic neuritis
  • 38 Abnormal ocular motor control
  • 39 Idiopathic intracranial hypertension (idiopathic pseudotumor cerebri)
  • 40 Giant cell arteritis
  • 41 Ischemic optic neuropathy
  • 42 Optic nerve axonal injury
  • 43 Leber's hereditary optic neuropathy
  • 44 Optic atrophy
  • 45 Nystagmus
  • 46 Toxic optic nerve neuropathies
  • Section 6 Oncology
  • 47 Uveal melanoma
  • 48 Genetics of hereditary retinoblastoma
  • 49 Molecular basis of low-penetrance retinoblastoma
  • 50 Vasculogenic mimicry
  • 51 Treatment of choroidal melanoma
  • 52 Sebaceous cell carcinoma
  • 53 Neurofibromatosis
  • Section 7 Other
  • 54 Phthisis bulbi
  • 55 Myopia
  • 56 Pathogenesis of Graves' ophthalmopathy
  • Section 8 Pediatrics
  • 57 Duane syndrome
  • 58 Amblyopia
  • 59 Strabismus
  • 60 Albinism
  • 61 Aniridia
  • Section 9 Retina
  • 62 Color vision defects
  • 63 Acute retinal vascular occlusive disorders
  • 64 Retinal photic injury: laboratory and clinical findings
  • 65 Vascular damage in diabetic retinopathy
  • 66 Neovascularization in diabetic retinopathy
  • 67 Diabetic macular edema
  • 68 Dry age-related macular degeneration and age-related macular degeneration pathogenesis
  • 69 Neovascular age-related macular degeneration
  • 70 Inhibition of
  • 71 Retinal detachment
  • 72 Retinopathy of prematurity
  • 73 Retinal energy metabolism
  • 74 Retinitis pigmentosa and related disorders
  • 75 Visual prostheses and other assistive devices
  • 76 Paraneoplastic retinal degeneration
  • 77 Cellular repopulation of the retina
  • 78 Proliferative vitreoretinopathy
  • Section 10 Uveitis
  • 79 Immunologic mechanisms of uveitis
  • 80 Herpesvirus retinitis
  • 81 Sympathetic ophthalmia
  • 82 Scleritis
  • 83 Infectious uveitis
  • 84 Ocular sarcoidosis
  • Index
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