Academic literature on the topic 'An Aid in the Diagnosis of Dry Eye Syndromes'

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Journal articles on the topic "An Aid in the Diagnosis of Dry Eye Syndromes"

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Candrea, Elisabeta, Cristina Pamfil, Lavinia Prodan, et al. "Dry Eye Disease in Systemic Lupus Erythematosus." Romanian Journal of Military Medicine 127, no. 4 (2024): 284–87. http://dx.doi.org/10.55453/rjmm.2024.127.4.5.

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: Systemic lupus erythematosus is a multi-organ autoimmune disease of unknown etiology characterized by widespread inflammation and significant morbidity and mortality. Organ affection includes joint and cutaneous involvement, pulmonary, neurological, and cardiac problems, renal and hematological involvement as well as ocular comorbidities, both posterior but mostly anterior ocular involvement. Therefore, we aimed to evaluate dry eye involvement in lupus patients. A cross-sectional study was performed with the aid of a web-based, anonymous questionnaire that was distributed to both patients di
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Al-Namaeh, Mashael. "Ocular manifestations of Parkinson disease." Medical Hypothesis, Discovery & Innovation in Optometry 1, no. 1 (2020): 1–10. http://dx.doi.org/10.51329/mehdioptometry101.

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Background: Parkinson's disease (PD) is the second most common neurodegenerative disorder. We aimed to review both the disease and the drug-related ocular manifestations of PD.
 Methods: In this manuscript, we have reviewed and summarized existing literature on the ocular manifestations and drug-related complications of PD. We have also discussed the use of current noninvasive imaging techniques, such as optical coherence tomography (OCT), for the early diagnosis and monitoring of PD.
 Results: Impaired color vision, reduced stereopsis, reduced contrast sensitivity, pupillary abnorma
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Lambert, Lester H., Noreen Shaikh, Jeffrey L. Marx, and David J. Ramsey. "End-stage crystalline maculopathy with retinal atrophy in Sjögren-Larsson syndrome: a case report and review of the literature." Therapeutic Advances in Rare Disease 3 (January 2022): 263300402211224. http://dx.doi.org/10.1177/26330040221122496.

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Sjögren-Larsson syndrome (SLS) is a rare, autosomal recessive neurocutaneous disorder. It is caused by the inheritance of sequence variants in the ALDH3A2 gene, which codes for fatty aldehyde dehydrogenase (FALDH). Universal signs of the condition are congenital ichthyosis, spastic paresis of the lower and upper limbs, and reduced intellectual ability. In addition to this clinical triad, patients with SLS experience dry eyes and decreased visual acuity caused by a progressive retinal degeneration. Examination of the retina in patients with SLS often reveals glistening yellow crystal-like depos
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Regis, Beatriz Cavalcanti, Ariadne Sampaio Toledo Fernandes, Laércio Pol-Fachin, and Daniela Sampaio Silva Gonçalves. "Doença do olho seco na era COVID-19: uma revisão de escopo." Research, Society and Development 11, no. 11 (2022): e122111133299. http://dx.doi.org/10.33448/rsd-v11i11.33299.

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O presente estudo busca correlacionar o uso da máscara facial e dispositivos eletrônicos na era COVID-19 com o surgimento ou agravamento da doença do olho seco. Bancos de dados online foram usados para identificar artigos publicados em 2020 e 2021, através dos descritores “dry eye syndromes”, “covid-19”, “diagnosis” e “asthenopia” encontrados no MeSH (Medical Subject Headings), associados ao operador booleano AND. Após a leitura dos títulos, resumos e textos na íntegra, dezessete artigos foram selecionados para compor o trabalho. Além disso, por indicação de especialista, o maior estudo mundia
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Pflugfelder, S. C. "Differential Diagnosis of Dry Eye Conditions." Advances in Dental Research 10, no. 1 (1996): 9–12. http://dx.doi.org/10.1177/08959374960100011801.

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The pre-ocular tear film is a complex biochemical structure produced by the lacrimal glands and epithelial cells on the ocular surface. Clinical syndromes of ocular irritation may result from deficiencies in one or more of these layers. At a recent dry eye workshop at the National Eye Institute, dry eye conditions were classified into those with adequate aqueous tear production and those with aqueous tear deficiency. The majority of patients with aqueous adequate dry eye suffer from meibomian gland dysfunction that results in lipid tear deficiency. Aqueous tear deficiency can be subclassified
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Abelson, Mark B., George W. Ousler, and Lauren A. Nally. "DRY EYE SYNDROMES: DIAGNOSIS, CLINICAL TRIALS, AND TREATMENT." Cornea 19, Supplement 2 (2000): S72. http://dx.doi.org/10.1097/00003226-200011002-00003.

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Nelson, J. Daniel, Alan Tomlinson, and Norihiko Yokoi. "Dry Eye Syndromes: Classification, Diagnosis & Outcome Measures." Ocular Surface 3 (January 2005): S31. http://dx.doi.org/10.1016/s1542-0124(12)70334-8.

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Odinaeva, K. N., N. S. Al Khateeb, and M. A. Frolov. "Dry eye syndrome in patients with gout." POINT OF VIEW. EAST – WEST, no. 4 (November 2, 2021): 6–11. http://dx.doi.org/10.25276/2410-1257-2021-4-6-11.

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Purpose. To determine and study the features of the development of dry eye syndrome (DES) in gout, depending on urate-lowering therapy, the duration of the gout disease and the concentration of uric acid in the tear. Material and methods. The study involved 149 male patients (261 eyes) aged 35 to 75 years (mean age 60.63 ± 11.00 years). Among them, 110 people (202 eyes) with an established diagnosis: "Cataract with concomitant gout disease" and 39 people (59 eyes) with cataracts without clinical and laboratory signs of gout. All patients underwent both standard ophthalmological examinations an
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Barrientos, Robinson T., Fernando Godín, Carlos Rocha-De-Lossada, et al. "Ophthalmological Approach for the Diagnosis of Dry Eye Disease in Patients with Sjögren’s Syndrome." Life 12, no. 11 (2022): 1899. http://dx.doi.org/10.3390/life12111899.

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Dry eye has two basic subdivisions: aqueous deficient dry eye (ADDE), with SS a major cause; and evaporative dry eye (EDE), due to either intrinsic or extrinsic factors. SS is a chronic inflammatory disorder defined by dysfunction of the exocrine glands leading to dry eye and dry mouth. The objective of this article was to carry out a systematic and critical review of several scientific publications on dry eye disease, with the aim of providing general recommendations to distinguish dry eye and its different variants in patients with SS, during the period 1979 to 2020, using search engines for
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Maurya, Rajendra P., Vibha Singh, Ashish Gupta, et al. "Dry eye disease associated with Primary Sjogren syndrome: An update." Indian Journal of Clinical and Experimental Ophthalmology 7, no. 2 (2021): 259–69. http://dx.doi.org/10.18231/j.ijceo.2021.055.

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Primary Sjögren’s syndrome (pSS) is a chronic, multisystem autoimmune disorder, characterized by mononuclear infiltration of exocrine glands and other organs, resulting in dry eye, dry mouth and extra-glandular systemic findings. Primary Sjögren syndrome is of particular interest to ophthalmologists as it constitutes an important differential diagnosis in conditions with dry eye disease. The ocular tests are of great importance for diagnosis and monitoring of primary sjogren’s syndrome. Also a better understanding of immunological mechanisms and molecular pathways have resulted in discovery of
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Dissertations / Theses on the topic "An Aid in the Diagnosis of Dry Eye Syndromes"

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Yedidya, Tamir. "Automatic detection of fluorescein tear breakup sequence." Phd thesis, 2010. http://hdl.handle.net/1885/150184.

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Dry Eye Syndrome is a common disease in the western world, with effects from uncomfortable itchiness to permanent damage to the ocular surface. Almost 5 million Americans over 50 years old suffer from dry eye. A conservative estimate shows that approximately 17 million Americans have contact lens related dry eye -one of the main factors to contact lens discontinuation. In addition, the incidence of the disease is on the rise. Nevertheless, there is still no gold standard test that can reliably detect dry eye. One of the most commonly used tests by clinicians to detect dry eye is the Fluorescei
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Books on the topic "An Aid in the Diagnosis of Dry Eye Syndromes"

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International Symposium on the Lacrimal System (6th 1990 Singapore). The lacrimal system. Kugler & Ghedini, 1991.

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Petrushkin, Harry, and Miles Stanford. The eye. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0024.

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The ophthalmologist has a large part to play in the management of many rheumatological diseases. These diseases can cause a number of symptoms from mild ocular discomfort to sudden blindness. In addition, many rheumatological diseases have helpful ophthalmic signs, which can aid diagnosis. This chapter has been written to help rheumatologists identify these signs and symptoms. We have started by summarizing the common pathology found in patients with rheumatological diseases (dry eye syndromes, conjunctivitis, episcleritis, scleritis, uveitis, and optic neuropathy). This has been arranged work
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Petrushkin, Harry, and Miles Stanford. The eye. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199642489.003.0024_update_001.

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The ophthalmologist has a large part to play in the management of many rheumatological diseases. These diseases can cause a number of symptoms from mild ocular discomfort to sudden blindness. In addition, many rheumatological diseases have helpful ophthalmic signs, which can aid diagnosis. This chapter has been written to help rheumatologists identify these signs and symptoms. We have started by summarizing the common pathology found in patients with rheumatological diseases (dry eye syndromes, conjunctivitis, episcleritis, scleritis, uveitis, and optic neuropathy). This has been arranged work
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Dry Eye Syndrome: Education for Patients and the Public. Exon Publications, 2025. https://doi.org/10.36255/dry-eye-syndrome.

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Dry Eye Syndrome is a common condition where the eyes do not produce enough quality tears, leading to discomfort, irritation, and vision problems. This article provides a comprehensive overview of the condition, including its definition, causes, symptoms, and treatment options. It explains how dry eye syndrome occurs, who is most at risk, and the different types that exist. The article also discusses how environmental and medical factors contribute to its development. The organization of the article follows a logical structure, beginning with an introduction that highlights the importance of t
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Dartt, Darlene A., David A. Sullivan, B. Britt Bromberg, et al. Lacrimal Gland, Tear Film, and Dry Eye Syndromes: Basic Science and Clinical Relevance. Springer, 2012.

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Lacrimal gland, tear film, and dry eye syndromes: Basic science and clinical relevance. Plenum Press, 1994.

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Dartt, Darlene A., David A. Sullivan, B. Britt Bromberg, Donald L. Mackeen, and Michelle M. Cripps. Lacrimal Gland, Tear Film, and Dry Eye Syndromes: Basic Science and Clinical Relevance. Springer London, Limited, 2012.

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Bijsterveld, O. P. Van, M. A. Lemp, and D. Spinelli. The Lacrimal System. Kugler Publications, 1991.

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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0127.

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Sjögren's syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren's syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren's syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0127_update_001.

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Sjögren’s syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren’s syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren’s syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Book chapters on the topic "An Aid in the Diagnosis of Dry Eye Syndromes"

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Rolando, Maurizio, Angelo Macrì, Trillo Carlandrea, and Giovanni Calabria. "Use of a Questionnaire for the Diagnosis of Tear Film-Related Ocular Surface Disease." In Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5359-5_114.

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Abelson, M. B., G. W. Ousler, L. A. Nally, and T. B. Emory. "Dry Eye Syndromes: Diagnosis, Clinical Trials and Pharmaceutical Treatment-‘Improving Clinical Trials’." In Advances in Experimental Medicine and Biology. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0717-8_152.

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Doane, Marshall G., and M. Estella Lee. "Tear Film Interferometry as a Diagnostic Tool for Evaluating Normal and Dry-Eye Tear Film." In Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5359-5_41.

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Feher, Janos. "Diagnostic Value of Tear Film Abnormalities in A New Syndrome Affecting the Neuroendocrine and Immune Systems." In Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5359-5_118.

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Yokoi, Norihiko, and Shigeru Kinoshita. "Importance of Conjunctival Epithelial Evaluation in the Diagnostic Differentiation of Dry Eye from Drug-Induced Epithelial Keratopathy." In Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5359-5_115.

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Switka-Więcławska, Iwona, Lidia Portacha, Tadeusz Kęcik, and Hanna Markiewicz. "The Significance of Salivary Gland Ultrasonography in the Diagnosis of Dry Eye Syndrome." In Advances in Experimental Medicine and Biology. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0717-8_173.

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Petrushkin, Harry, Duncan Rogers, and Miles Stanford. "The eye." In Oxford Textbook of Rheumatology. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0024_update_002.

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The ophthalmologist has a large part to play in the management of many rheumatological diseases. These diseases can cause a number of symptoms from mild ocular discomfort to sudden blindness. In addition, many rheumatological diseases have helpful ophthalmic signs, which can aid diagnosis. This chapter has been written to help rheumatologists identify these signs and symptoms. We have started by summarizing the common pathology found in patients with rheumatological diseases (dry eye syndromes, conjunctivitis, episcleritis, scleritis, uveitis, and optic neuropathy). This has been arranged work
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"https://exonpublications.com/index.php/exon/article/view/dry-eye-syndrome-types-causes-symptoms-treatments." In Dry Eye Syndrome: Education for Patients and the Public. Exon Publications, 2025. https://doi.org/10.36255/dry-eye-syndrome-types-causes-symptoms-treatments.

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Dry eye syndrome is a common condition that affects millions of people worldwide. It occurs when the eyes do not produce enough tears or when the tears evaporate too quickly, leading to discomfort and potential vision problems. This article provides a detailed guide on dry eye syndrome, covering its definition, prevalence, types, causes, symptoms, and pathophysiology. Diagnosis and complications are discussed, along with treatment options and strategies for managing the condition in daily life. The goal of this article is to provide clear, well-organized, and easy-to-understand information tha
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D. Rao, Pushpa. "Etiology of Dry Eye." In Dry Eye Disease Clinical Trial Endpoints - Current State of the Art and Future Perspectives [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.110142.

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The scope of this chapter is to provide insights into the classification based on the significant factors causing dry eye. The etiological causes of dry eye have been classified broadly into two primary arms. The first arm, aqueous deficient dry eye (ADDE), illustrates malfunction of normal lacrimal secretion causing tear hyposecretion. ADDE is subdivided into Sjogren’s and the non-Sjogren’s syndrome. The former exclusively includes systemic autoimmune characteristics, while the latter comprises age-related disorders, genetic disorders, denervation in the lacrimal gland, and obstruction in tea
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del Rosario Sánchez Valerio, María. "Current Diagnostic Tests for Dry Eye Disease in Sjögren’s Syndrome." In Eye Diseases - Recent Advances, New Perspectives and Therapeutic Options [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.103671.

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Sjogren’s syndrome (Sicca Syndrome) is mainly characterized by the presence of dry eye disease (DED). The diagnosis of DED in patients with Sjogren’s syndrome has been limited to tests such as the Schirmer test, tear breakup time (TBUT), and corneal stains; however, currently we can evaluate the functional unit in detail lacrimal, which is affected in patients with dry eye and Sjögren’s syndrome; thanks to technology that provides objective details for this difficult diagnostic. The newer evaluations that provide the greatest diagnostic value for Sjogren’s syndrome are: noninvasive keratograph
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Reports on the topic "An Aid in the Diagnosis of Dry Eye Syndromes"

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Zhang, Yingrong, Sanchun Tan, Jieyu Wang, et al. A scoping review protocol of systematic reviews and meta-analyses to acupuncture for the treatment of peripheral facial paralysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.3.0084.

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Review question / Objective: To conduct a systematic comprehensive review for Acupuncture treatment of peripheral facial paralysis and to evaluate the efficacy and safety of acupuncture therapy for peripheral facial paralysis. Condition being studied: Peripheral facial paralysis, known as peripheral facial never palsy, includes Bell’s palsy and Ramsay Hunt syndrome.Any medical conditions such as infection, malignancy and autoimmune issues can result it. Idiopathic Bell's palsy is the most common disease causing peripheral facial nerve palsy, which clinical features include unilateral weakness
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