Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy [0.03%]
既往诊断SLE与首次肾活检诊断SLE的临床对比分析
Pantipa Tonsawan,Kittisak Sawanyawisuth
Pantipa Tonsawan
Background: Lupus nephritis is a type of major organ involvement in systemic lupus erythematosus (SLE) patients that leads to higher rates of morbidity and mortality and may present initially in 28% of SLE patients. Howev...
Current laboratory and clinical practices in reporting and interpreting anti-nuclear antibody indirect immunofluorescence (ANA IIF) patterns: results of an international survey [0.03%]
抗核抗体间接免疫荧光（ANA IIF）模式的报告和解释的现行实验室和临床实践：一项国际调查的结果
Lieve Van Hoovels,Sylvia Broeders,Edward K L Chan et al.
Lieve Van Hoovels et al.
Background: The International Consensus on Antinuclear Antibody (ANA) Patterns (ICAP) has recently proposed nomenclature in order to harmonize ANA indirect immunofluorescence (IIF) pattern reporting. ICAP distinguishes co...
Castleman disease and SLE in a G6PD-deficient Marfan patient: a case report and literature review [0.03%]
G6PD缺乏的马方综合征患者的卡斯特曼病和SLE：病例报告及文献复习
Sami Alhoulaiby,Lina Okar,Haya Samaan et al.
Sami Alhoulaiby et al.
Introduction: Marfan syndrome, G6PD deficiency, systemic lupus erythematosus (SLE), and Castleman disease are four distinctive, thoroughly investigated entities whose coincidence was never reported. However, occurrence in...
Association between autoimmune diseases and COVID-19 as assessed in both a test-negative case-control and population case-control design [0.03%]
自身免疫疾病与COVID-19的关联性评估：基于测试阴性病例对照和人群病例对照设计的研究
Rossella Murtas,Anita Andreano,Federico Gervasi et al.
Rossella Murtas et al.
Background: COVID-19 epidemic has paralleled with the so called infodemic, where countless pieces of information have been disseminated on putative risk factors for COVID-19. Among those, emerged the notion that people su...
Human placental extract attenuates neurological symptoms in the experimental autoimmune encephalomyelitis model of multiple sclerosis-a putative approach in MS disease? [0.03%]
人胎盘提取物减轻多发性硬化症实验自身免疫性脑脊髓炎模型的神经症状－一种对MS疾病的假定治疗方法？
Mir Hadi Jazayeri,Khadijeh Barzaman,Reza Nedaeinia et al.
Mir Hadi Jazayeri et al.
Background: Different studies have demonstrated the anti-inflammatory effects of human placental extract both in vivo and in vitro. Considering the chronic inflammatory nature of multiple sclerosis (MS) disease, we examin...
Autoantibodies directed against α1-adrenergic receptor and endothelin receptor A in patients with prostate cancer [0.03%]
前列腺癌患者体内抗α1-肾上腺素受体和内皮素受体A的自身抗体研究
Gerd Wallukat,Burkhard Jandrig,Niels-Peter Becker et al.
Gerd Wallukat et al.
Background: For prostate cancer, signaling pathways induced by over-boarding stimulation of G-protein coupled receptors (GPCR) such as the endothelin, α1- and β-adrenergic, muscarinic and angiotensin 1 receptors were ac...
Quality and best practice in medical laboratories: specific requests for autoimmunity testing [0.03%]
医学实验室的质量和最佳实践：自身免疫检测的特殊要求
Ulrich Sack,Xavier Bossuyt,Hristina Andreeva et al.
Ulrich Sack et al.
Special conditions associated with laboratory autoimmune testing are not well compatible with recent developments in regulatory frameworks such as EN/ISO 15189 accreditation or in vitro diagnostic medical device regulation (IVD-R). In addit...
Renato Tozzoli,Nicola Bizzaro
Renato Tozzoli
Recurrent angioedema, Guillain-Barré, and myelitis in a girl with systemic lupus erythematosus and CD59 deficiency syndrome [0.03%]
系统性红斑狼疮和CD59缺陷综合征女患者的复发性血管神经水肿、吉兰-巴雷综合征和脊髓炎
Vadood Javadi Parvaneh,Leila Ghasemi,Khosro Rahmani et al.
Vadood Javadi Parvaneh et al.
Background: CD59 deficiency is a congenital mutation disorder in complement pathway which can present with various manifestations. Case presentation: ...
Profiles of criteria and non-criteria anti-phospholipid autoantibodies are associated with clinical phenotypes of the antiphospholipid syndrome [0.03%]
抗磷脂综合征临床表型与抗磷脂抗体谱系的关系
Ilan Volkov,Luciana Seguro,Elaine P Leon et al.
Ilan Volkov et al.
Background: Specific anti-phospholipids antibodies (aPLs) are used as classification criteria of the antiphospholipid syndrome (APS). These aPLs, although essential for diagnosis, do not predict disease phenotypes, which ...