1. PM-Scl1抗体阳性: PM-Scl代表“多发性肌炎/硬皮病重叠综合征”(Polymyositis/Scleroderma overlap syndrome)的抗体。当这种抗体检测呈阳性时,它通常与多发性肌炎、硬皮病或两者重叠的综合征有关。 患者可能会出现肌肉无力、皮肤硬化和其他与这些疾病相关的症状。 2. SMD1抗体阳性: SMD1是与系统性硬化症(也称为...
SMD Storage Module Device (interface standard for disk drives) SMD ScanMail for Domino (software) SMD Senior Managing Director SMD State Military Department (various locations) SMD Severely Mentally Disabled SMD Syndrome Myélodysplasique (French: Myelodysplastic Syndrome) SMD Storage Module Drive SMD Se...
manhooddeathsyndrome, SMDS) 朱少华 华中科技大学同济医学院法医学系 湖北同济法医学司法鉴定中心 是一种原因未明的猝死。 青壮年猝死综合征这一名称自日本渡边富雄1977年提 出以来,在法医检验中逐渐引起人们的重视。SMDS在国 外文献中报道较多,但国内报告的相对较少。
High-risk patients include those with refractory anemia, sideroblastic anemia, 5q- syndrome, patients with a good prognosis (low or lower intermediate international prognosis score), patients having received over 100 RBC units, and patients under the age of 70. Deferoxamine, while it can prevent ...
Tlje Peutz-Jeghers SmdromeTlje Peutz-Jeghers SmdromeIn 1921 in Holland, Peutz1 first reported this interesting condition. Later, more elaborate attention was given to the syndrome by Jeghers, 2 and finally, in 1954, Bruwer et al3 bestowed the title of" Peutz-Jeghers syndrome" on this unusua...
产品别名: AGS 1; AGS1; AGS-1; Aicardi Goutieres syndrome 1; ATIP; ATM and Rad3 related interacting protein; ATM and Rad3-related-interacting protein; ATR interacting protein; ATR-interacting protein; Atrip; ATRIP_HUMAN; Deoxyribonuclease III dnaQ/mutD (E. coli) like; DKFZp434J0310; DKFZ...
the industry’s emphasis on creativity means that professionals are often expected to come up with fresh, innovative ideas on demand. This can cause a great deal of pressure and can lead to self-doubt and imposter syndrome. It’s important for those in the marketing sector to prioritise their...
Dans un contexte clinique évocateur, le diagnostic biologique de syndrome myélodysplasique (SMD) ou de leucémie myélomonocytaire chronique (LMMC) repose toujours en 2023 principalement sur l’intégration des données issues d’analyses cytologiques médullaires et sanguines auxquelles s’ajoutent...
THE SUPERIOR VENA CAVA SYNDROME; DIAGNOSTIC AND SURGICAL CONSIDERATIONS, CASE REPORTS Three cases of the superior vena cava syndrome are detailed, two of benign etiology and one due to malignancy. Surgery was performed to overcome the venous... EL Lowenberg,W Hotchkiss,S Mcdaniel - 《Diseases of...
There is increasing evidence that mutations affecting human CNTN4 structure may be associated with 3p deletion syndrome5 and/or autism spectrum disorders (ASD)9,48. Recent studies indicate that the absence of CNTN4 or its binding partner APP49 in neuronal cells has an impact on target-specific ...