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• Ch. 1 Historical perspective of developmental glaucomas
• Ch. 2 Terminology and classification of developmental glaucomas
• Ch. 3 Embryologic basis of developmental glaucomas
• Ch. 4 Epidemiology and genetics of developmental glaucomas
• Ch. 5 Pathology and pathogenesis of developmental glaucomas
• Ch. 6 Primary congenital glaucoma
• Ch. 7 Secondary congenital glaucoma
• Ch. 8 Overview of the management of developmental glaucomas
• Ch. 9 Medical therapy of pediatric glaucoma
• Ch. 10 Initial surgical treatment of congenital glaucoma
• Ch. 11 Simultaneous surgery for bilateral congenital glaucoma
• Ch. 12 Management of refractory pediatric glaucoma
• Ch. 13 Penetrating keratoplasty in children with developmental glaucomas
• Ch. 14 Glaucomas in aphakia and pseudophakia after congenital cataract surgery
• Ch. 15 Management of residual vision in pediatric glaucoma.

• Ch. 1 General eye examination / Maria Aaron, Wayne A. Solley, Geoffrey Broocker
• Ch. 2 Ophthalmic differential diagnosis / David A. Palay
• Ch. 3 The red eye / Jay H. Krachmer
• Ch. 4 Eyelid abnormalities / Ted H. Wojno
• Ch. 5 Conjunctival abnormalities / David A. Palay
• Ch. 6 Corneal abnormalities / David A. Palay
• Ch. 7 Scleritis / Michael C. Diesenhouse -- Ch. 8 Lens abnormalities / Jonathan H. Engman, Andrew R. Harrison, Jay H. Krachmer
• Ch. 9 Uveitis / Terry Kim, Douglas M. Blackmon
• Ch. 10 Retina / Timothy W. Olsen
• Ch. 11 Glaucoma / Allen D. Beck
• Ch. 12 Neuro-ophthalmology / Timothy J. Martin
• Ch. 13 Pediatric ophthalmology / Arlene V. Drack
• Ch. 14 Orbital disease / Ted H. Wojno
• Ch. 15 Systemic disease and therapies / Emmett F. Carpel
• Ch. 16 Ocular trauma / Geoffrey Broocker, Wayne A. Solley
• Ch. 17 Guide to ophthalmic medications / Geoffrey Broocker, Michael D. Bennett
• Index.

Primary Care Ophthalmology is your ideal source for the most essential information on eye disease. You'll find reviews of relevant anatomy and pathophysiology followed by easy to use outlines of the symptoms, signs, differential diagnoses, treatments, and referral indications for the ophthalmic conditions you are most likely to see in practice. With its clear focus on diagnosis and treatment, this point-of-care reference brings evidenced-based, clinically actionable information to the front lines of primary care. The free, PocketConsult handheld software package provides all the clinical text from the book. Illustrations from the book are also available in an electronic format for optional download. Text is written mostly in easily accessible outline form, making the reference quick and efficient. Abundant full-color illustrations include precise labels, insets, and schematics to accurately correspond to the related text. Succinct coverage provides need-to-know information on symptoms, etiology, workup, and treatment without becoming bogged down in unnecessary details. The PocketConsult PDA software optionally includes all illustrations from the text for reference on the move. All instances where sight loss is possible are highlighted. Both the book and the PDA software contain an extensive Ophthalmic Formulary.

• The assessment of vision / David Sculfor and Bruce James
• The slit lamp / Bruce James
• Tonometry / Bruce James
• Gonioscopy / Bruce James
• Examination of the retina and optic disc / Larry Benjamin and Bruce James
• Optical and anatomical assessment of the cornea / Larry Benjamin
• Testing the visual field / Bruce James
• Examination of the orbit and ocular adnexae / Ramona Khooshabeh and Larry Benjamin
• Ocular motility examination / Manoj V. Parulekar
• The pupils / Bruce James
• Microbiological examination and investigation / Larry Benjamin
• Ultrasound techniques in ophthalmology B-scan ultrasound / Carlos Eduardo Solarte
• Colour Doppler imaging / Asifa Shaikh
• Biometry / David Sculfor
• Radiological techniques in ophthalmic investigation / Gerardine Quaghebeur
• Clinical visual electrophysiology / Richard Smith and David Sculfor
• Fluorescein angiography / Larry Benjamin
• New imaging techniques / Andrew McNaught.

• Induction of Type 2 Diabetes in Mice to Understand Vascular Changes that Drive Diabetic Retinopathy
• Akimba Proliferative Diabetic Retinopathy Model: Understanding Molecular Mechanism and Drug Screening for the Progression of Diabetic Retinopathy
• Oxygen-Induced Retinopathy in the Rat: An Animal Model to Study the Proliferative Retinal Vascular Pathology
• Retinal Assessment Using In Vivo Electroretinography and Optical Coherence Tomography in Rodent Models of Diabetes
• A Guide to Genome Wide Association Study Design for Diabetic Retinopathy
• Single Cell RNA Sequencing (scRNA-Seq) Data Analysis of Retinal Homeostasis and Degeneration of Microglia
• Bioinformatics Tools for Bulk Gene Expression Deconvolution in Diabetic Retinopathy
• MicroRNA Profiling from Tears as a Potential Non-Invasive Method for Early Detection of Diabetes Retinopathy
• Proximity Extension Assay (PEA) Platform to Detect Vitreous Biomarkers of Diabetic Retinopathy
• Methods for Analyzing the Gut Microbiota in Diabetic Retinopathy
• Mass Spectrometry-Based Vitreous Proteomics: Validated Methods and Analysis Pipeline
• Methods for Ex Vivo AAV Transduction in Rodent and Human Retinal Explants
• Methods for RPE Sheet Construction Using iPS-CM in Conjunction with Natural Scaffold of Corneal Lenticule Derived from SMILE
• Chromatin Immunoprecipitation Assay in Mouse Retinal Tissue
• Frozen Block Tissue Staining for Eye Structure of Zebrafish Embryo
• Investigating the Function of MicroRNAs in Human Retinal Microvascular Endothelial Cells of Diabetic Retinopathy
• Genome Editing Inhibits Retinal Angiogenesis in a Mouse Model of Oxygen-Induced Retinopathy

This detailed volume provides various cellular and experimental animal models and research methodologies to understand the complex interrelated pathophysiological mechanisms triggered by hyperglycemia that underlie the development of diabetic retinopathy. The book covers methods for understanding the pathogenesis of diabetic retinopathy, detection and screening of biomarkers in diabetic retinopathy, as well as novel technologies for diabetic retinopathy management. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step and readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Diabetic Retinopathy: Methods and Protocols serves as an invaluable resource for scientists and clinicians who are interested in the area of ophthalmology research

• Optic Nerve Hypoplasia
• Optic Nerve Coloboma
• Morning Glory Disc Anomaly
• Optic Nerve Pit
• Myelinated retinal nerve fiber layer
• Optic Nerve Drusen
• Papilledema from Idiopathic Intracranial Hypertension
• Papilledema from Secondary Pseudotumor Cerebri
• Papilledema from Dural Sinus Thrombosis
• Optic neuritis associated with Multiple Sclerosis
• Optic Neuritis associated with MOG-IgG Positivity
• Optic Neuritis associated with Neuromyelitis Optica
• Neuroretinitis
• Optic Nerve Glioma in Neurofibromatosis Type I
• Optic Nerve Glioma (Sporadic)
• Optic Nerve Sheath Meningioma in the setting of Neurofibromatosis Type II
• Optic Nerve Infiltration in the setting of a Brain Tumor
• Dominant Optic Atrophy
• Leber Hereditary Optic Neuropathy
• Nutritional Optic Neuropathy from Vitamin A Deficiency
• Congenital Fibrosis of the Extraocular Muscles
• Duane Syndrome
• Moebius Syndrome
• Third Nerve Palsy
• Fourth Nerve Palsy
• Sixth Nerve Palsy
• Acute Acquired Comitant Esotropia
• Ocular Myasthenia Gravis
• Chronic Progressive External Ophthalmoplegia
• Ocular Neuromyotonia
• Infantile-onset saccade initiation delay (ISID) or congenital ocular motor apraxia
• Infantile Nystagmus
• Paroxysmal Tonic Downgaze in Infancy
• Spasmus Nutans
• Russell Diencephalic Syndrome of Infancy with Monocular Nystagmus
• Nystagmus associated with a Retinal Dystrophy
• Downbeat Nystagmus
• Opsoclonus Myoclonus Syndrome
• Horner Syndrome
• Anisocoria from a Third Nerve Palsy
• Craniopharyngioma
• Dorsal Midbrain Syndrome
• Posterior Fossa Tumor
• Craniosynostosis with Papilledema
• Ataxia Telangiectasia
• Neuronal Ceroid Lipofuscinosis
• Adrenoleukodystrophy
• Joubert Syndrome with Congenital Fibrosis of the Extraocular Muscles
• KIF11 Mutation
• Cerebral/Cortical Visual Impairment (CVI)
• Non-Organic Vision Loss

Fundamentals of Pediatric Neuro-Ophthalmology is the first case-based textbook dedicated to pediatric neuro-ophthalmology. Fundamentals is a must-have resource for ophthalmologists, neurologists, emergency medicine physicians, and pediatricians who are seeking a practical guide for the diagnosis and management of pediatric neuro-ophthalmologic disease. With contributions from experts in the Consortium of Pediatric Neuro-ophthalmologists, the text is an important educational reference for trainees and established physicians alike. Key Features Fifty-two real-world clinical cases that examine presenting symptoms and signs, differential diagnosis, approach to evaluation, treatment considerations, visual outcomes, and novel insights into disease management Broad coverage of important topics in pediatric neuro-ophthalmology including Congenital optic nerve anomalies Optic disc edema Optic nerve tumors Optic atrophy Strabismus Disorders of the extraocular muscles Nystagmus Other abnormal eye movements Pupillary disorders Neuro-ophthalmologic manifestations in neurologic and systemic diseases Higher order visual processing disorders Video library of important clinical signs of neuro-ophthalmologic disease Discussion of decision making and interpretation of ancillary testing by experts in the field of pediatric neuro-ophthalmology Easy to follow format that will serve as a concise, practical guide with clinical pearls and references for further reading

• Cover
• Title
• Contents
• Chapter 1 Screening: The Rationale and Feasibility
• Chapter 2 Whom to Screen
• Chapter 3 Location of Screening Activity
• Chapter 4 Program Management Timelines
• Chapter 5 Conforming with Regulation
• Chapter 6 Prescreening Protocol
• Chapter 7 Information, Education and Communication
• Chapter 8 The Team
• Chapter 9 Community Participation
• Chapter 10 Equipment Checklist
• Chapter 11 On Site Checklist
• Chapter 12 The RationPatient Flow
• Chapter 13 Standard Operating Procedures
• Chapter 14 Postscreening Follow-up
• Chapter 15 Efficacy Measures

• 1. Ocular Surface Anatomy and Physiology
• 2. Phlyctenular disease, ocular rosacea and the role of the eyelid margin in ocular surface diseases of children
• 3. Allergic and atopic disease of the pediatric eye
• 4. Infectious Conjunctivitis in Children
• 5. Ocular Surface Lesions in Children
• 6. Pediatric ocular graft versus host disease and dry eye disease
• 7. Ophthalmic Manifestations of Stevens-Johnson Syndrome and Mycoplasma Induced Rash and Mucositis in Children
• 8. Pediatric Neurotrophic Keratopathy
• 9. The Role of Contact Lenses in the Management of Ocular Surface Disease in Children
• 10. Surgical Rehabilitation of the Ocular Surface in Children

Ocular surface diseases in children have not always been well understood and the literature in this age group is limited. The consequences of misdiagnosis and delayed diagnosis include visually significant scarring and amblyopia, thus with real impact on their quality of life and ultimate visual potential. Recently, there has been an increase in clinical and research focus on these diseases, contributing to a growing awareness of their importance to pediatric visual health. This book is the first comprehensive volume dedicated to pediatric ocular surface diseases. It provides an up-to-date and highly illustrated discussion of the pathophysiology, symptomatology and diagnostic and therapeutic strategies of these less commonly understood diseases, in a format that is readily absorbed by trainees and seasoned physicians alike. The aim of this book is to provide a practical and detailed understanding of ocular surface disease in the pediatric population, as many of these corneal conditions in children require unique therapeutic approaches and may have subtle presentations. Chapters will address key issues, such as dry eye disease, Steven Johnson Syndrome and neurotrophic keratitis, that can have a profound impact on childrens visual and social development. Pediatric Ocular Surface Disease is a must-have resource for pediatric ophthalmology fellows, cornea fellows, pediatric ophthalmologists, and cornea specialists

• 1. General Guidelines For Pediatric Retinal Surgery
• 2. Conservative Interventions For Retinal Diseases
• 3. Surgical Management Of Pediatric Retinal Vascular Disorders
• 4. Developmental Disorders
• 5. Inflammatory Disorders
• 6. Pediatric Rhegmatogenous Retinal Detachment
• 7. Pediatric Ocular Trauma
• 8. Posterior Segment Hemorrhages
• 9. Retinoblastoma
• 10. Miscellaneous Management Topics
• 11. Visual Rehabilitation

This book provides practical information on how to approach pediatric retinal diseases especially with respect to surgical indications and decisions as well as tips and key points for surgical techniques. Clear and concise chapters highlight pearls, pitfalls and related basic knowledge elements which are supported by video clips to provide a unique reference. Pediatric Vitreoretinal Surgery is an essential guide for ophthalmologists, ophthalmology residents, vitreoretinal fellows and practicing vitreoretinal surgeons seeking a key resource to support their daily practice for pediatric retinal diseases. Questions and answers via app: Download the Springer Nature Flashcards app free of charge to test your knowledge on pediatric vitreoretinal surgery

• High Resolution Imaging Mass Spectrometry of Human Donor Eye: Photoreceptor Cells and Basal Laminar Deposits of Age-related Macular Degeneration
• The non-canonical role of Complement Factor H in Retinal Pigment Epithelium (RPE) cells and implications for Age-related Macular Degeneration
• Macular Pigment Carotenoids and Bisretinoid A2E
• Disturbed matrix metalloproteinases activity in age-related macular degeneraton
• Current views on Chr10q26 contribuiton to age-related macular degeneration
• Untargeted lipidomic profiling of aged human retina with and without age-related macular degeneration (AMD)
• Decoding Race and Age-Relation Macular Degeneration: GPR 143 Activity is the Key
• Peroxisome proliferator-activated receptor gamma coactivator 1 alpha ( PGC-1x): a transcriptional regulator at the interface of aging and age-related macular degeneration?
• Regulation of ABCA1 by miR-33 and miR-34a in the aging eye
• The role of gene expression regulation on genetic risk of Age-related Macular Degeneration
• Elastin layer in Bruch's membrane as a target for immunizatio or tolerization to modulate patthology in the mouse model of somke-induced ocular injury
• Repuprosing drugs for treatment of age-relation macular degeneration
• Extracellular Vesicle RNA Contents as Biomarkers for Ocular Diseases
• Proteomics of retinal extracellular vesicles: a reviw inot an unexplored mechanism in retinal health and AMD pathogenesis
• Prime Editing Strategy to Instally the PRHP2 c.828+1G A mutations
• Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing
• Generation of an Avian Myeloblastosis Virus (AMV) Reverse Transcriptase Prime Editor
• Pre-existing neutralizing antibodies against different adeno-associated virus serotypes in humans and large animal models for gene therapy
• Optimization of Capillary-based Western Blotting for MYO7A
• AAV Serotypes and Their Suitability for Retinal Gene Therapy
• Gene Augmentation ofautosomal dominant CRX-associated retinopathies
• Txnip gene therapy of retinitis pigmentosa improves cone health Factors affecting readthrough of natural versus premature termination codons
• Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative Disease
• Network biology and medcine to resuce: Applications for retinal disease mechanisms and therapy
• Non-sydromic Retinal Degeneration Caused by Pathogenic Variants in Joubert Syndrome Genes
• Exonic variants that affect splicing- an opportunity for "hidden" mutations causing inherited retinal diseases
• Enhanced S-cone Syndrome, a Mini-Review
• The role of microglia in Inherited Retinal Diseases
• CD68: potential contributor to inflammation and RPE cell dystrophy
• Gene Expression of Clusterin, Tissue Inhibitor of Metalloproteinase-1, and Their receptors in Retinal Pigment Epithelial Cells and Muller Glial Cells is Modulated by Inflammatory Stresses
• Axonal Transport Defects in Retinal Ganglion Cells
• Connexins biology in the pathophysiology of retinal diseases
• Role of Nuclear NAD +in Retinal Homeostasis
• Retinal pigmented epithelium-derived ectopic norrin does not promote intraretinal angiogenesis in transgenic mice
• Caveolin-1 Muller glia exist as heat-resistant, high molecular weight complexes
• Role of VLC-PUFAs in Retinal and Macular Degeneration
• Ocular amyloid , condensates, and aggregates - higher order protein assemblies participate in both retinal degeneration and function
• Photoreceptor ion channels in signaling and disease
• The role of peripherin-2 /ROM1 complexes in photoreceptor outer segment disc morphogenesis
• Human mutations in Arl3, a small GTPase involved inlipidated cargo delibery to the cilia cause retinatl dystropthy
• Genotype-Phenotype Association in ABCA4-Associated Retinopathy
• Retinal pathoconnectomics: A Window into Neurodegeneration
• The role of Ceramide in Inherited Retinal Disease Pathology
• Extracelluar Matix: the Unexplored Aspects of Retinal Pathologies and Regeneration
• Role of TFEB in diseases assocaited with lysosomal dysfunction
• Retinoic acid receptor -related oprhan receptors (RORs) in eye development and disease
• A novel mouse model for Late-Onset Retinal Degeneration (L-ORD) devekios RPE abnormalities due to the loss of C1qtnf5/Ctrp5
• Comparison of mouse models of autosomal dominant retinitis pigmentosa due to P23H muations of Rhodopsin
• Compensatory Cone-Mediated Mechanisms in Inherited Retinal Degeneration Mouse Models: A Functional and Gene Expression Analsyis
• Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Sress and Promotes ER Protein Degradation in Cyclic Nucleotide-gated Channel Deficiency
• Mouse choroid proteome revisited: foucs on aging
• Morphological and functional comparison of mice models for retinitis pigmentosa
• Current Advancements in Mouse Models of Retinal Disease
• Single-cell Itrnacriptomic Profiling of Muller Glia in the rd10 Retina
• Methods for in vivo characterization of proteostatis in the mouse retina
• Absence or PRCD leads to dysregulation in lipie Homeostatis resulting in disorganizationof photorecptor outer segment structure
• Expansion Microscopy of Mouse Photoreceptro Cilia
• Rod photorecptor specific ablation of Metformin target, AMPK, in preclinical model of autosomal recessvie retinitis pigmentosa
• TLR2 is highly overexpressed in retinal myeloid cells in the rd10 mouse model of retinitis pigmentosa
• Environmental light has an essentail effrect on the diseasae expression in a dominant RPE65 mutation
• Microglia Preserve Visual Function in A Mouse Model of Retinitis Pigmentosa with Rhodopsin-P23H Mutant
• Measuring the release of lactate from wild-type and rd1 mouse retina
• Aerobic glycolysis in photorecptors supports energy demand in the absence of mitochondrial coupling
• Redox Status in Retinitis Pigmentosa
• Perspectives on retinal dolichol metabolism and visual deficits in dolichol metalbolism-associated inherited disorders
• Retinal metabolic profile on IMPG2 deficiency mice with subretinal lesions
• Glutathione-coating of liposomes enhances the delivery of hydrophillic cargo to the inner nuclear layer in retinal cultures
• Modification of Mueller glial cell fate and proliferation with the use of small molecules
• A potential neuroprotective role for pyruvate kinase 2 in retinal degeneration
• Critical role of VEGF as a direct regulator of photorecptor function
• Lysine Ubiquitylation Drives Rhodopsin Protein Turnover
• In-silico prediction of MYO!C Rhodopsin Interactions and its Significance in Protein Localization and Visual Function
• A ciliary branched actin netowrk drives photoreceptor disc morphogenesis
• Revisiting the daily timing of POS phagocytosis
• Inhibition of Bacterial Peoptidoglycan Cytopahty by Retina Pigment Epithelial PGRP2 Amidase
• Understanding ischemic retinopathies: the role of Succinate and its recpto^T mutation
• Inducing neural regeneratio nfrom glia using proneural bHLH transcription factors

This book contains the proceedings of the XIX International Symposium on Retinal Degeneration. A majority of those who spoke and presented posters at the meeting contributed to this volume. The blinding diseases of inherited retinal degenerations have no treatments, and age-related macular degeneration has no cures, despite the fact that it is an epidemic among the elderly, with 1 in 3-4 affected by the age of 70. The RD Symposium focused on the exciting new developments aimed at understanding these diseases and providing therapies for them. These retinal degeneration symposia are known by most as the best and most important meetings in the field. The volume presents representative state-of-the-art research in almost all areas of retinal degenerations, ranging from cytopathologic, physiologic, diagnostic and clinical aspects; animal models; mechanisms of cell death; candidate genes, cloning, mapping and other aspects of molecular genetics; and developing potential therapeutic measures such as gene therapy and neuroprotective agents for potential pharmaceutical therapy. We anticipate that the excitement of those working in the field and those afflicted with retinal degenerations is reflected in the volume

• Differential diagnosis of ocular symptoms
• Differential diagnosis of ocular signs
• Trauma
• Cornea
• Conjunctiva/sclera/iris/external disease
• Eyelid
• Orbit
• Pediatrics
• Glaucoma
• Neuro-ophthalmology
• Retina
• Uveitis
• General ophthalmic problems
• Imaging modalities in ophthalmology.

"A best-selling source of compact, authoritative guidance on the treatment of ocular disorders in a variety of settings, The Wills Eye Manual, 8th Edition, is the comprehensive, high-yield reference of choice for both trainees and seasoned practitioners. It provides highly illustrated information on more than 200 ophthalmic conditions along with proven clinical recommendations from initial diagnosis through extended treatment. The consistent, bulleted outline format makes it ideal for portability and quick reference. Provides current, superbly illustrated information on more than 200 ophthalmic conditions in a handy, portable manual, along with extensive multimedia content. Features easily accessible clinical recommendations for evaluation, diagnosis, management, and treatment. Contains updates on the latest major clinical trials in ophthalmology, as well as two expertly produced new videos and many new clinical images added. Addresses changing trends in oculoplastics, glaucoma, cornea, pediatrics, neuro-ophthalmology, uveitis, retina, and more. Includes videos depicting a wide range of common procedures with step-by-step narration, carefully selected to complement key techniques. All chapters written and edited by the residents and attending ophthalmologists at one of the busiest and largest eye hospitals in the country"-- Provided by publisher

• Automated Analysis for Retinopathy of Prematurity by Deep Neural Networks
• DeepROP : an Automated ROP Screening System
• Diagnosis of Diabetic Retinopathy Using Deep Neural Networks
• Automated Identification and Grading System of Diabetic Retinopathy Using Deep Neural Networks
• Automated segmentation of macular edema in OCT using deep neural networks
• DeepUWF : An Automated Ultra-wide-field Fundus Screening System via Deep Learning
• DeepUWF-Plus : Automatic Fundus Identification and Diagnosis System Based on Ultrawide-field Fundus Imaging

• Preface
• Acknowledgements
• Abbreviations and acronyms
• 1. Introduction
• 2. Methodology
• 3. Results and discussions
• Summary of findings, suggestions and conclusion
• Bibliography
• Index

Study conducted in Tiruchchirāppalli District, Tamil Nadu, India

• Part 1: Introduction
• Chapter 1.Implantation of artificial intraocular lenses-a brief history (Thomas Neuhann)
• Chapter 2. Epidemiology (Lukas Bisorca-Gassendorf)
• Chapter 3. Anatomy and physiology of the anterior segment (Andreas Ohlmann)
• Chapter 4. Cataract forms and grading (Christopher Wirbelauer)
• Chapter 5. Optical principles (Kerstin Petermann)
• Chapter 6. Digital Lens insurgery (Wolfgang J. Mayer)
• Part 2: Examination
• Chapter 7. Medical history (Johannes H. Burger)
• Chapter 8. Testing of visual function: visual acuity refraction contrast sensitivity (Bettina von Livonius)
• Chapter 9. Assessment of optical phenomena (Gernot Steinwender)
• Chapter 10. Slit lamp examination (Gernot Steinwender)
• Chapter 11. Binocular vison and motility (Oliver Ehrt)
• Chapter 12. Measurement of intraocular pressure (Matthias Nobl)
• Chapter 13. Eyelids (Christoph Hintschich)
• Chapter 14. Optical biometry (Oliver Findl)
• Chapter 15. Scheimpflug tomography and measurement of higher order aberrations (Jens Bhren)
• Chapter 16. OCT of the anterior segment (Nikolaus Luft)
• Chapter 17. OCT of the posterior segment (Jakob Siedlecki)
• Chapter 18. Measurement of endothelial cells (Gernot Steinwender)
• Chapter 19. Tear film analysis (Anna Maria Schuh)
• Chapter 20. Pupillometry (Helmut Wilhelm)
• Chapter 21. Congenital and childhood cataract: Examination and indication for newborns and children (Gnther Rudolph)
• Chapter 22. Anaesthesia for cataract surgery (Friedrich Lersch)
• Part 3: Choosing the right lens.-Chapter 23. Design and material of intraocular lenses (Gerd U. Auffarth)
• Chapter 24. General introduction to IOL calculation (Peter Hoffmann)
• Chapter 25. Formula optimisation and use of the IOL WEB platform IOLCon (Achim Langenbucher).

This book summarizes the current knowledge on lens surgery. Not only are the surgical procedures described in detail, but experts share with the reader many useful practical tips for individual surgical steps to achieve the best possible surgical result. In addition to the focus on surgery, pre- and post-operative care and complication management is also discussed in detail and a systematic review of the current literature is provided. Clear and concisely written chapters highlight topics such as the use of special lenses, femto-laser lens surgery, secondary lens implantation and phakic lens surgery throughout the book. Cataract and Lens Surgery offers a practical resource for ophthalmologists who perform lens surgery in their daily clinical practice. Clinicians navigating the different types of lens preparations and properties for routine to complex procedures will find this book to be an essential guide.

This groundbreaking resource gives you full details on state-of-the-art 2D and 3D eye imaging and modeling techniques that are paving the way to breakthrough clinical applications in eye health. It’s the first book to explore in depth a new generation of computational methods that combine image processing, simulation, and statistical discrimination tools in efforts to improve early detection of cataracts, diabetic retinopathy, glaucoma, iridocyclitis, corneal haze, maculopathy, and other visual impairments and conditions