{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T23:41:10Z","timestamp":1784590870502,"version":"3.55.0"},"reference-count":11,"publisher":"Galenos Yayinevi","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["FVVO"],"DOI":"10.52054\/fvvo.2025.62","type":"journal-article","created":{"date-parts":[[2025,6,11]],"date-time":"2025-06-11T02:59:42Z","timestamp":1749610782000},"source":"Crossref","is-referenced-by-count":5,"title":["Euro-Chinese consensus on accessory cavitated uterine malformation*,\u2020"],"prefix":"10.52054","author":[{"given":"Lan","family":"Zhu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zichen","family":"Zhao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Attilio","family":"Di Spiezio Sardo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maribel","family":"Aci\u00e9n","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joel","family":"Naftalin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thierry","family":"Van den Bosch","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charleen","family":"Sze-yan Cheung","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dabao","family":"Xu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaowu","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Grigoris","family":"Grimbizis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"2811","published-online":{"date-parts":[[2025,6,11]]},"reference":[{"issue":"17","key":"ref0","doi-asserted-by":"publisher","first-page":"1729","DOI":"10.1056\/NEJMoa0801560","article-title":"Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease","volume":"360","author":"Hara","year":"2009","unstructured":"1. Hara K, Shiga A, Fukutake T, et al. Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. N Engl J Med 2009; 360(17): 1729-1739.","journal-title":"N Engl J Med"},{"key":"ref1","doi-asserted-by":"publisher","unstructured":"2. Yao T, Zhu J, Wu X, et al. Heterozygous HTRA1 mutations cause cerebral small vessel diseases: genetic, clinical, and pathologic findings from 3 Chinese pedigrees. Neurol Genet 2022 ;8(6): e200044.","DOI":"10.1212\/NXG.0000000000200044"},{"issue":"5","key":"ref2","doi-asserted-by":"publisher","first-page":"817","DOI":"10.1212\/WNL.58.5.817","article-title":"Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy","volume":"58","author":"Yanagawa","year":"2002","unstructured":"3. Yanagawa S, Ito N, Arima K, et al. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. Neurology 2002; 58(5): 817-820.","journal-title":"Neurology"},{"issue":"5","key":"ref3","doi-asserted-by":"publisher","first-page":"459","DOI":"10.1212\/WNL.0000000000001803","article-title":"Characteristic features and progression of abnormalities on MRI for CARASIL","volume":"85","author":"Nozaki","year":"2015","unstructured":"4. Nozaki H, Sekine Y, Fukutake T, et al. Characteristic features and progression of abnormalities on MRI for CARASIL. Neurology 2015; 85(5): 459-463.","journal-title":"Neurology"},{"issue":"4","key":"ref4","doi-asserted-by":"publisher","first-page":"1110","DOI":"10.1161\/STROKEAHA.114.006735","article-title":"Shifting the CARASIL paradigm: report of a non-Asian family and literature review","volume":"46","author":"Cordeiro","year":"2015","unstructured":"5. Cordeiro IM, Nzwalo H, S\u00e1 F, et al. Shifting the CARASIL paradigm: report of a non-Asian family and literature review. Stroke 2015; 46(4): 1110-1112.","journal-title":"Stroke"},{"issue":"3","key":"ref5","doi-asserted-by":"publisher","first-page":"182","DOI":"10.5505\/tbdhd.2024.82542","article-title":"Fatal cerebellar hemorrhage in a patient with CARASIL","volume":"30","author":"Kanat","year":"2024","unstructured":"6. Kanat S, Kay\u0131m Y\u0131ld\u0131z \u00d6, Balaban H, et al. Fatal cerebellar hemorrhage in a patient with CARASIL. Turk J Cerebrovasc Dis 2024; 30(3): 182-187.","journal-title":"Turk J Cerebrovasc Dis"},{"issue":"2","key":"ref6","doi-asserted-by":"publisher","first-page":"85","DOI":"10.1016\/j.jstrokecerebrovasdis.2010.11.008","article-title":"Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification","volume":"20","author":"Fukutake","year":"2011","unstructured":"7. Fukutake T. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification. J Stroke Cerebrovasc Dis 2011; 20(2): 85-93.","journal-title":"J Stroke Cerebrovasc Dis"},{"key":"ref7","doi-asserted-by":"publisher","first-page":"240","DOI":"10.4274\/tnd.2021.91298","article-title":"Clinical and molecular genetic findings of cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","volume":"27","author":"R\u00fcstemo\u011flu","year":"2021","unstructured":"8. R\u00fcstemo\u011flu BS, Samanci B, Tepge\u00e7 F, et al. Clinical and molecular genetic findings of cerebral arteriopathy with subcortical infarcts and leukoencephalopathy. Turk J Neurol 2021; 27: 240-247.","journal-title":"Turk J Neurol"},{"issue":"11","key":"ref8","doi-asserted-by":"publisher","first-page":"3447","DOI":"10.1161\/STROKEAHA.114.004236","article-title":"Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy","volume":"45","author":"Nozaki","year":"2014","unstructured":"9. Nozaki H, Nishizawa M, Onodera O. Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. Stroke 2014; 45(11): 3447-3453.","journal-title":"Stroke"},{"key":"ref9","doi-asserted-by":"publisher","first-page":"123229","DOI":"10.1016\/j.jns.2024.123229","article-title":"HTRA1-related cerebral small-vessel disease causes cerebral microbleeds on the brainstem surface","volume":"466","author":"Kobayashi","year":"2024","unstructured":"10. Kobayashi Y, Kondo Y, Tazawa KI, et al. HTRA1-related cerebral small-vessel disease causes cerebral microbleeds on the brainstem surface. J Neurol Sci 2024; 466: 123229.","journal-title":"J Neurol Sci"},{"issue":"11","key":"ref10","doi-asserted-by":"publisher","first-page":"106029","DOI":"10.1016\/j.jstrokecerebrovasdis.2021.106029","article-title":"Two unique mutations in HTRA1-related cerebral small vessel disease in North America and Africa and literature review","volume":"30","author":"Shang","year":"2021","unstructured":"11. Shang T, Pinho M, Ray D, et al. Two unique mutations in HTRA1-related cerebral small vessel disease in North America and Africa and literature review. J Stroke Cerebrovasc Dis 2021; 30(11): 106029.","journal-title":"J Stroke Cerebrovasc Dis"}],"container-title":["Facts Views and Vision in ObGyn"],"original-title":[],"deposited":{"date-parts":[[2025,7,25]],"date-time":"2025-07-25T08:19:04Z","timestamp":1753431544000},"score":1,"resource":{"primary":{"URL":"https:\/\/fvvo.eu\/articles\/euro-chinese-consensus-on-accessory-cavitated-uterine-malformationlesssupgreaterlesssupgreater\/doi\/FVVO.2025.62"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,6,11]]},"references-count":11,"URL":"https:\/\/doi.org\/10.52054\/fvvo.2025.62","relation":{},"ISSN":["2032-0418","2684-4230"],"issn-type":[{"value":"2032-0418","type":"print"},{"value":"2684-4230","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025,6,11]]}}}