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Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric Center原发性噬血细胞性淋巴组织细胞增多症:一种具有多种基因型特征和结局的严重免疫失调性疾病:一项来自三级儿科中心的研究
Ozturk, Ahmet Gokcan; Haskologlu, Zehra Sule; Cakmakli, Hasan Fatih; Islamoglu, Candan; Ileri, Talia; Ince, Elif; Ozdemir, Sonay Incesoy; Dincaslan, Handan Ugur; Tacyildiz, Nurdan; Unal, Emel Cabi; Dogu, Figen; Ertem, Mehmet; Ikinciogullari, Aydan
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收藏 Expression of Immune Checkpoints LAG-3, CTLA-4, TIM-3, and PD-1 in Beta-Thalassemia Patients Treated Using HbF Augmentation Therapy and Regular Transfusionsβ地中海贫血患者经胎儿血红蛋白增强疗法和定期输血治疗后LAG-3、CTLA-4、TIM-3和PD-1免疫检查点的表达
Khan, Komal; Khan, Umaima; Shah, Asma; Shah, Syed Muhammad Ikram; Khan, Yousaf; Khan, Muhammad Tariq Masood; Rani, Gulab Fatima
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