バイヤーズ症候群
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
- Immunoinhibitory checkpoint deficiency in medium and large vessel vasculitis.
- Zhang H1, Watanabe R1, Berry GJ2, Vaglio A3, Liao YJ4, Warrington KJ5, Goronzy JJ1, Weyand CM6.
- Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2017 Feb 7;114(6):E970-E979. doi: 10.1073/pnas.1616848114. Epub 2017 Jan 23.
- Giant cell arteritis (GCA) causes autoimmune inflammation of the aorta and its large branches, resulting in aortic arch syndrome, blindness, and stroke. CD4+ T cells and macrophages form organized granulomatous lesions in the walls of affected arteries, destroy the tunica media, and induce ischemic
- PMID 28115719
- Perioperative Retinal Artery Occlusion: Risk Factors in Cardiac Surgery from the United States National Inpatient Sample 1998-2013.
- Calway T1, Rubin DS2, Moss HE3, Joslin CE4, Beckmann K5, Roth S6.
- Ophthalmology.Ophthalmology.2017 Feb;124(2):189-196. doi: 10.1016/j.ophtha.2016.10.025. Epub 2016 Nov 30.
- PURPOSE: To study the incidence and risk factors for retinal artery occlusion (RAO) in cardiac surgery.DESIGN: Retrospective study using the National Inpatient Sample (NIS).METHODS: The NIS was searched for cardiac surgery. Retinal artery occlusion was identified by International Classification of D
- PMID 27914836
- Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22.
- Byers HM1,2, Adam MP2,3, LaCroix A3, Leary SE4, Cole B5, Dobyns WB2,3,6,7, Mefford HC2,3.
- American journal of medical genetics. Part A.Am J Med Genet A.2017 Jan;173(1):245-249. doi: 10.1002/ajmg.a.37993. Epub 2016 Oct 12.
- Atypical teratoid rhabdoid tumors of the central nervous system are rare, highly malignant, embryonal tumors most often occurring in children under age 3 years. Most are due to a somatic change in tumor suppressor gene SMARCB1 followed by a second-hit, typically loss of heterozygosity, best detected
- PMID 27734605
Japanese Journal
- Ehlers-Danlos syndrome : recent advances and current understanding of the clinical and genetic heterogeneity
- Marfan syndrome: Abnormal 2 chain in type I collagen
Related Links
- Byers syndrome symptoms, causes, diagnosis, and treatment information for Byers syndrome (Cholestasis, progressive familial intrahepatic 1) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments ...
- Dr. Byers, Director of the Collagen Diagnostic Laboratory (CDL) discusses Vascular Ehlers-Danlos Syndrome. Learn more at www.edsawareness.com
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