{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T07:13:22Z","timestamp":1785222802499,"version":"3.55.0"},"reference-count":17,"publisher":"Japanese Society of Internal Medicine","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Intern. Med."],"published-print":{"date-parts":[[2018]]},"DOI":"10.2169\/internalmedicine.8624-16","type":"journal-article","created":{"date-parts":[[2017,10,31]],"date-time":"2017-10-31T22:12:13Z","timestamp":1509487933000},"page":"319-324","source":"Crossref","is-referenced-by-count":15,"title":["Clinical Features of Hereditary and Mast Cell-mediated Angioedema Focusing on the Differential Diagnosis in Japanese Patients"],"prefix":"10.2169","volume":"57","author":[{"given":"Isao","family":"Ohsawa","sequence":"first","affiliation":[{"name":"Nephrology Unit, Saiyu Soka Hospital, Japan"},{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daisuke","family":"Honda","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Atsuko","family":"Hisada","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"},{"name":"Department of Nephrology, Ikegami General Hospital, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hiroyuki","family":"Inoshita","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kisara","family":"Onda-Tsueshita","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Satoshi","family":"Mano","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nobuyuki","family":"Sato","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"},{"name":"Deprtment of Internal Medicine, Niigata Rosai Hospital, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuya","family":"Nakamura","sequence":"additional","affiliation":[{"name":"Nephrology Unit, Saiyu Soka Hospital, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tatsuo","family":"Shimizu","sequence":"additional","affiliation":[{"name":"Nephrology Unit, Saiyu Soka Hospital, Japan"},{"name":"Department of Internal Medicine, Saiyu Kawaguchi Clinic, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hiromichi","family":"Gotoh","sequence":"additional","affiliation":[{"name":"Nephrology Unit, Saiyu Soka Hospital, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshikazu","family":"Goto","sequence":"additional","affiliation":[{"name":"Nephrology Unit, Saiyu Soka Hospital, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yusuke","family":"Suzuki","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Internal Medicine, Juntendo University Faculty of Medicine, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuhiko","family":"Tomino","sequence":"additional","affiliation":[{"name":"Medical Corporation SHOWAKAI, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"962","reference":[{"key":"1","doi-asserted-by":"crossref","unstructured":"1. Zuraw BL. Hereditary angioedema. N Engl J Med 359: 1027-1036, 2008.","DOI":"10.1056\/NEJMcp0803977"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Craig T, P\u00fcrs\u00fcn EA, Bork K, et al. WAO guideline for the management of hereditary angioedema. World Allergy Organ J 5: 182-199, 2012.","DOI":"10.1097\/WOX.0b013e318279affa"},{"key":"3","unstructured":"3. Bygum A. Hereditary angio-oedema in Denmark: a nationwide survey. Br J Dermatol 161: 1153-1158, 2009."},{"key":"4","unstructured":"4. Psarros F, Koutsostathis N, Farmaki E, Speletas MG, Germenis AE. Hereditary angioedema in Greece: the first results of the Greek hereditary angioedema registry. Int Arch Allergy Immunol 164: 326-332, 2014."},{"key":"5","unstructured":"5. Roche O, Blanch A, Caballero T, Sastre N, Callejo D, L\u00f3pez-Trascasa M. Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain. Ann Allergy Asthma Immunol 94: 498-503, 2005."},{"key":"6","doi-asserted-by":"publisher","unstructured":"6. Jolles S, Williams P, Carne E, et al. A UK national audit of hereditary and acquired angioedema. Clin Exp Immunol 175: 59-67, 2014.","DOI":"10.1111\/cei.12159"},{"key":"7","unstructured":"7. Ohsawa I, Honda D, Nagamachi S, et al. Clinical manifestations, diagnosis, and treatment of hereditary angioedema: survey data from 94 physicians in Japan. Ann Allergy Asthma Immunol 114: 492-498, 2015."},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Amar SM, Dreskin SC. Urticaria. Prim Care 35: 141-157, vii-viii, 2008.","DOI":"10.1016\/j.pop.2007.09.009"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Bork K. Angioedema. Immunol Allergy Clin North Am 34: 23-31, 2014.","DOI":"10.1016\/j.iac.2013.09.004"},{"key":"10","unstructured":"10. Kozel MM, Bossuyt PM, Mekkes JR, Bos JD. Laboratory tests and identified diagnoses in patients with physical and chronic urticaria and angioedema: a systematic review. J Am Acad Dermatol 48: 409-416, 2003."},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Lang DM, Aberer W, Bernstein JA, et al. International consensus on hereditary and acquired angioedema. Ann Allergy Asthma Immunol 109: 395-402, 2012.","DOI":"10.1016\/j.anai.2012.10.008"},{"key":"12","unstructured":"12. Agostoni A, Ayg\u00f6ren-P\u00fcrs\u00fcn E, Binkley KE, et al. Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol 114: S51-S131, 2004."},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Horiuchi T, Ohi H, Ohsawa I, et al. Guideline for hereditary angioedema (HAE) 2010 by the Japanese Association for Complement Research - secondary publication. Allergol Int 61: 559-562, 2012.","DOI":"10.2332\/allergolint.12-RAI-0471"},{"key":"14","unstructured":"14. Zanichelli A, Magerl M, Longhurst H, Fabien V, Maurer M. Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe. Allergy Asthma Clin Immunol 9: 29, 2013."},{"key":"15","unstructured":"15. Bork K, Meng G, Staubach P, Hardt J. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am J Med 119: 267-274, 2006."},{"key":"16","unstructured":"16. Bygum A, Ayg\u00f6ren-P\u00fcrs\u00fcn E, Caballero T, et al. The hereditary angioedema burden of illness study in Europe (HAE-BOIS-Europe): background and methodology. BMC Dermatol 12: 4, 2012."},{"key":"17","unstructured":"17. Hauptmann G, Goetz J, Uring-Lambert B, Grosshans E. Component deficiencies: 2. The fourth component. Prog Allergy 39: 232-249, 1986."}],"container-title":["Internal Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/57\/3\/57_8624-16\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,10,5]],"date-time":"2019-10-05T11:47:39Z","timestamp":1570276059000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/57\/3\/57_8624-16\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018]]},"references-count":17,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2018]]}},"URL":"https:\/\/doi.org\/10.2169\/internalmedicine.8624-16","relation":{},"ISSN":["0918-2918","1349-7235"],"issn-type":[{"value":"0918-2918","type":"print"},{"value":"1349-7235","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018]]}}}