WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- British sculptor (born in the United States) noted for busts and large controversial works (1880-1959) (同)Jacob Epstein, Sir Jacob Epstein
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
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- 1. エプスタインバーウイルス（EBウイルス）感染の臨床的特徴および治療 clinical manifestations and treatment of epstein barr virus infection
- 2. エプスタインバーウイルス（EBウイルス）のウイルス学 virology of epstein barr virus
- 3. 血球貪食リンパ組織球の臨床的特徴および診断 clinical features and diagnosis of hemophagocytic lymphohistiocytosis
- 4. Acute genital ulceration (Lipschütz ulcer) acute genital ulceration lipschutz ulcer
- 5. 非ホジキンリンパ腫の病理の概要 overview of the pathobiology of the non hodgkin lymphomas
English Journal
- Congenital thrombocytopenia with nephritis - The first case of MYH9 related disorder in Serbia.
- Kuzmanović M, Kunishima S, Putnik J, Stajić N, Paripović A, Bogdanović R.
- Vojnosanitetski pregled. Military-medical and pharmaceutical review.Vojnosanit Pregl.2014 Apr;71(4):395-8.
- INTRODUCTION: The group of autosomal dominant disorders - Epstein syndrome, Sebastian syndrome, Fechthner syndrome and May-Hegglin anomaly - are characterised by thrombocytopenia with giant platelets, inclusion bodies in granulocytes and variable levels of deafness, disturbances of vision and renal
- PMID 24783421
- Successful renal transplantation in MYH9-related disorder with severe macrothrombocytopenia: first report in Korea.
- Min SY1, Ahn HJ2, Park WS1, Kim JW3.
- Transplantation proceedings.Transplant Proc.2014 Mar;46(2):654-6. doi: 10.1016/j.transproceed.2013.11.144.
- MYH9-related disorders (MYH9 RD) are genetic disorders by the variation of MYH9 gene that encodes for the nonmuscle myosin heavy chain IIA. The clinical and laboratory findings of Fechtner syndrome, an MYH9 RD, are macrothrombocytopenia, basophilic cytoplasmic inclusion bodies in leukocytes, glomeru
- PMID 24656038
Japanese Journal
- Sustained elevation of serum interleukin-18 and its association with hemophagocytic lymphohistiocytosis in XIAP deficiency
- Wada Taizo,Kanegane Hirokazu,Ohta Kazuhide,Katoh Fumiyo,Imamura Toshihiko,Nakazawa Yozo,Miyashita Ritsuko,Hara Junichi,Hamamoto Kazuko,Yang Xi,Filipovich Alexandra H.,Marsh Rebecca A.,Yachie Akihiro
- Cytokine 65(1), 74-78, 2014-01
- … X-linked lymphoproliferative syndrome (XLP) is a rare primary immunodeficiency characterized by increased vulnerability to Epstein-Barr virus infection. …
- NAID 120005349175
- 臨床研究・症例報告 特発性ネフローゼ症候群初発症例とヒトパルボウイルスB19およびEBウイルス感染の関連性の検討
- 岡本 さつき,松岡 雄一郎,遠海 重裕 [他]
- 小児科臨床 66(11), 2241-2244, 2013-11
- NAID 40019828529
Related Links
- Epstein, A.A., U.S. physician, 1880-1965. Epstein syndrome - symptoms include edema, protein concentration in urine, low concentration of albumin in the blood ... Disclaimer All content on this website, including dictionary ...
- Epstein's Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. ... Epstein's Syndrome: Introduction Epstein's Syndrome: A syndrome ...
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| 拡張検索 | 「van Bogaert-Scherer-Epstein syndrome」 |
| 関連記事 | 「syndrome」 |
「van Bogaert-Scherer-Epstein syndrome」
「syndrome」
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