{"doi":"10.1076/ocii.11.4.277.18260","title":"Changing patterns of intraocular inflammatory disease in Japan","abstract":null,"journal":"Ocular Immunology and Inflammation","year":2003,"id":628859,"datarank":0.7909499337845621,"base_score":5.272999558563747,"endowment":5.272999558563747,"self_citation_contribution":0.7909499337845621,"citation_network_contribution":0.0,"self_endowment_contribution":0.7909499337845621,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":194,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1628384,"name":"Yoshihiro Morimura","orcid":null,"position":1,"is_corresponding":false},{"id":549624,"name":"Yuko Miyamoto","orcid":null,"position":2,"is_corresponding":false},{"id":1005682,"name":"Annabelle A. Okada","orcid":"0000-0002-8850-8962","position":3,"is_corresponding":false},{"id":1628382,"name":"Toshiko Wakabayashi","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"Changing patterns of intraocular inflammatory disease in Japan","abstract":"PURPOSE: We investigated the frequencies and clinical characteristics of Japanese patients with uveitis. METHODS: Records of 189 patients referred from April 1999 to March 2001 were retrospectively reviewed. RESULTS: Fifty-six patients (29.6%) had anterior uveitis, 13 (6.9%) intermediate uveitis, 59 (31.2%) posterior uveitis, 58 (30.7%) panuveitis, and three (1.6%) papillitis. The most common diagnoses were Vogt-Koyanagi-Harada (VKH) disease (10.1%), biopsy-proven or presumed sarcoidosis (9.5%), acute anterior uveitis (7.9%), tuberculosis (6.9%), and Behçet's disease (5.8%). Seventy-three patients (38.6%) were treated with local therapy alone, and 95 patients (50.3%) required systemic therapy. Ocular complications developed in 19.6% of patients, and systemic complications in 2.1%. CONCLUSIONS: These results confirm a continued high frequency of VKH disease and sarcoidosis, but suggest a decreased frequency of Behçet's disease and an increased frequency of tuberculosis. Roughly one-half of the patients required systemic treatment in addition to local therapy, and ocular and/or systemic complications developed in one-fifth of the patients.","is_dataset_classified":null,"base_score":5.272999558563747,"endowment":5.272999558563747,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"14704899","pmcid":null,"openalex_id":"https://openalex.org/W2021497829","authors":[],"funders":[],"total_grants":0,"fwci":2.6033,"citation_percentile":0.88317267,"influential_citations":0,"citation_trend":[{"year":2012,"count":7},{"year":2013,"count":13},{"year":2014,"count":14},{"year":2015,"count":9},{"year":2016,"count":24},{"year":2017,"count":20},{"year":2018,"count":10},{"year":2019,"count":7},{"year":2020,"count":9},{"year":2021,"count":10},{"year":2022,"count":7},{"year":2023,"count":7},{"year":2024,"count":3},{"year":2025,"count":6},{"year":2026,"count":1}],"oa_status":"closed","license":null,"oa_locations":[{"url":"http://www.tandfonline.com/doi/pdf/10.1076/ocii.11.4.277.18260","host_type":"publisher"},{"url":"https://doi.org/10.1076/ocii.11.4.277.18260","host_type":"journal"},{"url":"https://pubmed.ncbi.nlm.nih.gov/14704899","host_type":"repository"}],"fields_of_study":["Ocular Diseases and Behçet’s Syndrome","Sarcoidosis and Beryllium Toxicity Research","Otitis Media and Relapsing Polychondritis"],"mesh_terms":["Adolescent","Adult","Aged","Aged, 80 and over","Behcet Syndrome","Child","Female","Humans","Japan","Male","Middle Aged","Retrospective Studies","Sarcoidosis","Tuberculosis, Ocular","Uveitis","Uveomeningoencephalitic Syndrome"],"keywords":["Medicine","Uveitis","Sarcoidosis","Vogt–Koyanagi–Harada disease","Tuberculosis","Systemic disease","Dermatology","Behcet's disease","Retrospective cohort study","Medical record","Disease","Intermediate uveitis","Surgery","Ophthalmology","Anterior uveitis","Internal medicine","Pathology"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Good health and well-being"}],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-08-05T15:23:29.791494Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}