Evolution and trends of childhood cataract research in the past 10 years: A scientometric analysis
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Zhenzhen Liu | L. Luo | Hui Chen | Guangming Jin | Yanyu Shen | Y. Tan | Yingshi Zou | Shaoyi Gong
[1] T. Ahmad,et al. Global research trends in MERS-CoV: A comprehensive bibliometric analysis from 2012 to 2021 , 2022, Frontiers in Public Health.
[2] R. Tuuminen,et al. Evaluation of IOL power calculation with the Kane formula for pediatric cataract surgery , 2022, Graefe's Archive for Clinical and Experimental Ophthalmology.
[3] W. Lagrèze,et al. Pediatric cataract surgery: Rate of secondary visual axis opacification depending on intraocular lens type. , 2022, Ophthalmology.
[4] Mohammed A. Al-Sharafi,et al. A Scientometric Analysis and Systematic Literature Review for Construction Project Complexity , 2022, Buildings.
[5] A. Yaman,et al. Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement , 2021, Metabolic Brain Disease.
[6] Marcus Ang,et al. Artificial intelligence for anterior segment diseases: Emerging applications in ophthalmology , 2020, British Journal of Ophthalmology.
[7] M. E. Wilson,et al. Globe Axial Length Growth at Age 10.5 Years in the Infant Aphakia Treatment Study. , 2020, American journal of ophthalmology.
[8] A. Hutchinson,et al. Outcomes of Unilateral Cataracts in Infants and Toddlers 7 to 24 Months of Age: Toddler Aphakia and Pseudophakia Study (TAPS). , 2019, Ophthalmology (Rochester, Minn.).
[9] L. Liang,et al. Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing , 2019, Molecular genetics & genomic medicine.
[10] Xiaohang Wu,et al. Diagnostic Efficacy and Therapeutic Decision-making Capacity of an Artificial Intelligence Platform for Childhood Cataracts in Eye Clinics: A Multicentre Randomized Controlled Trial , 2019, EClinicalMedicine.
[11] Peter M. Krawitz,et al. Identifying facial phenotypes of genetic disorders using deep learning , 2019, Nature Medicine.
[12] G. Cardona,et al. Quality of life among parents of children with visual impairment: A literature review. , 2018, Research in developmental disabilities.
[13] P. Cumberland,et al. 5-year outcomes after primary intraocular lens implantation in children aged 2 years or younger with congenital or infantile cataract: findings from the IoLunder2 prospective inception cohort study. , 2018, The Lancet. Child & adolescent health.
[14] L. Reis,et al. Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genes , 2018, Human Genetics.
[15] J. V. von Oettingen,et al. High rates of ocular complications in a cohort of Haitian children and adolescents with diabetes , 2018, Pediatric diabetes.
[16] V. Werth,et al. Prevention and management of glucocorticoid-induced side effects: A comprehensive review: Ocular, cardiovascular, muscular, and psychiatric side effects and issues unique to pediatric patients. , 2017, Journal of the American Academy of Dermatology.
[17] Salil A. Lachke,et al. Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract , 2016, Human Genetics.
[18] I. C. Lloyd,et al. Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach , 2016, Eye.
[19] A. Fielder,et al. Global prevalence of childhood cataract: a systematic review , 2016, Eye.
[20] M. Amador,et al. Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood , 2016, Orphanet Journal of Rare Diseases.
[21] A. Sigurdson,et al. The Risk of Cataract among Survivors of Childhood and Adolescent Cancer: A Report from the Childhood Cancer Survivor Study , 2016, Radiation Research.
[22] Shaochen Chen,et al. Lens regeneration using endogenous stem cells with gain of visual function , 2016, Nature.
[23] K. Holman,et al. Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing , 2016, Human mutation.
[24] P. Bonnen,et al. Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes. , 2015, Molecular genetics and metabolism.
[25] A. Haidich,et al. Complications and Visual Outcomes After Secondary Intraocular Lens Implantation in Children. , 2015, American journal of ophthalmology.
[26] L. Bielory,et al. Over-the-counter migration of steroid use: impact on the eye , 2014, Current opinion in allergy and clinical immunology.
[27] S. Freedman,et al. Illuminated Microcatheter–facilitated 360-Degree Trabeculotomy for Refractory Aphakic and Juvenile Open-angle Glaucoma , 2014, Journal of glaucoma.
[28] W. Pu,et al. Ten-year etiologic review of Chinese children hospitalized for pediatric cataracts. , 2014, Eye science.
[29] F. Alkuraya,et al. Juvenile cataract morphology in 3 siblings not yet diagnosed with cerebrotendinous xanthomatosis. , 2013, Ophthalmology.
[30] Sheila T. Angeles-Han,et al. Prevention and Management of Cataracts in Children with Juvenile Idiopathic Arthritis–Associated Uveitis , 2012, Current Rheumatology Reports.
[31] T. Olsen,et al. Risk of glaucoma after pediatric cataract surgery. , 2008, Investigative ophthalmology & visual science.
[32] Terry Kim,et al. Cataracts , 2017, The Lancet.
[33] C. Cheung,et al. Pediatric Uveitis , 2018, Asia-Pacific journal of ophthalmology.
[34] I. C. Lloyd,et al. Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric Cataract. , 2016, Ophthalmology.