アダマンティアデス・ベーチェット症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
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
UpToDate Contents
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English Journal
- Genetic Analysis of RNF213 c.14576G>A Variant in Nonatherosclerotic Quasi-Moyamoya Disease.
- Miyawaki S1, Imai H2, Shimizu M3, Yagi S3, Ono H2, Nakatomi H2, Shimizu T3, Saito N2.
- Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.J Stroke Cerebrovasc Dis.2015 May;24(5):1075-9. doi: 10.1016/j.jstrokecerebrovasdis.2015.01.005. Epub 2015 Mar 25.
- BACKGROUND: Quasi-moyamoya disease (MMD) and MMD (definite MMD) have similar cerebral angiographic features, but whether these related diseases have similar etiology or genetic background remains unclear. Recently, we have reported that the recently identified MMD susceptibility gene variant RNF213
- PMID 25817623
- Lally L1, Spiera RF2.
- Rheumatic diseases clinics of North America.Rheum Dis Clin North Am.2015 May;41(2):315-331. doi: 10.1016/j.rdc.2015.01.004. Epub 2015 Feb 27.
- Pulmonary vasculitis encompasses inflammation in the pulmonary vasculature with involved vessels varying in caliber from large elastic arteries to capillaries. Small pulmonary capillaries are the vessels most commonly involved in vasculitis affecting the lung. The antineutrophil cytoplasmic antibody
- PMID 25836645
- Apremilast for Behçet's syndrome--a phase 2, placebo-controlled study.
- Hatemi G1, Melikoglu M, Tunc R, Korkmaz C, Turgut Ozturk B, Mat C, Merkel PA, Calamia KT, Liu Z, Pineda L, Stevens RM, Yazici H, Yazici Y.
- The New England journal of medicine.N Engl J Med.2015 Apr 16;372(16):1510-8. doi: 10.1056/NEJMoa1408684.
- BACKGROUND: Oral ulcers, the hallmark of Behçet's syndrome, can be resistant to conventional treatment; therefore, alternative agents are needed. Apremilast is an oral phosphodiesterase-4 inhibitor that modulates several inflammatory pathways.METHODS: We conducted a phase 2, multicenter, placebo-co
- PMID 25875256
Related Links
- Aetiology Adamantiades–Behçet's syndrome is a systemic inflammatory disease seen frequently among the Japanese and among the population of the Mediterranean basin. Hence it is often called the Silk Road disease.
- Adamantiades-Behcet’s disease (ABD) is a chronic, relapsing, systemic vasculitis of unknown etiology. It is more prevalent in populations along the ancient Silk Road from Eastern Asia to the Mediterranean Basin, and ...
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- Adamantiades-Behcet syndrome
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- ベーチェット病
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ベーチェット症候群