Sitosterolemia with Compound Heterozygous Variants in the ABCG5 Gene: A Rare Cause of Non-immune Hemolysis and Macrothrombocytopenia [0.03%]
ABCG5基因复合杂合变异所致 sitosterolemia 一例及相关非免疫性溶血和大细胞性血小板减少症罕见病因分析
Başak Bostankolu Değirmenci,Hamza Polat
Başak Bostankolu Değirmenci
Cameron Perry,Xinyu Von Buttlar,Swapna Thota
Cameron Perry
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, chronic bone marrow failure condition characterized by complement-mediated hemolytic anemia and thrombosis. Since its initial clinical description in 1882, somatic mutations in PIG-A were...
Öznur Aydın,Mehmet Turgut
Öznur Aydın
Primary Gastric Extranodal NK/T Cell Lymphoma with T Cell Phenotype: A Very Rare EBV-Related Locally Involved Aggressive T Cell Lymphoma Case and the Therapeutic Effects of COVID-19 Infection [0.03%]
原发胃黏膜相关外周T细胞型NK/T细胞淋巴瘤一例及COVID-19感染对其的影响
Derya Koyun,Seher Yüksel,Muhit Özcan et al.
Derya Koyun et al.
Large and Multi-Nuclei Blasts in Hypotriploid Karyotype and TP53 Mutation Acute Myeloid Leukemia with P210 BCR::ABL1 Transcript [0.03%]
低三倍体核型和TP53突变急性髓系白血病中存在P210BCR::ABL1融合 transcript的病例发生大细胞和多核胞性原始粒细胞浸润现象
Yihong Huangchuan,Xueyan Chen
Yihong Huangchuan
Exploration of Leucine Rich Alpha-2-Glycoprotein 1 (LRG1) and its Association with Proangiogenic Mediators in Sickle Cell Disease: A Potential Player in the Pathogenesis of the Disease [0.03%]
裂头珠蛋白1(LRG1)在溶血性疾病的表达及其与促血管生成介质的关系：疾病发病机制中的潜在作用因子探索研究
Oğuzhan Özcan,Murat Kaçmaz,Fatma Hazal Erdoğan et al.
Oğuzhan Özcan et al.
Objective: Leucine rich alpha-2-glycoprotein 1 (LRG1) is a novel mediator involved in the abnormal angiogenesis. We aimed to investigate circulating LRG1 levels and their relationship with proangiogenic mediators in sickl...
Optical Genome Mapping - A New Approach To Detecting Cytogenetic Abnormalities: Why is it Difficult in Multiple Myeloma? [0.03%]
光学基因组测序技术在检测染色体异常领域的新应用及在多发性骨髓瘤中难以实现的原因分析研究
Ayşe Gül Bayrak Tokaç,Mehmet Burak Mutlu,Simge Erdem et al.
Ayşe Gül Bayrak Tokaç et al.
Fatty Precipitation in Donor Bone Marrow Caused by Overnight Cold Preservation in a Refrigerator [0.03%]
骨髓捐献者夜间冷藏保存导致的脂肪沉底现象
Osamu Imataki,Tomohiro Kaji,Makiko Uemura
Osamu Imataki
Unusual Comorbid Condition in a Child with Severe Factor XI Deficiency: Spina Bifida [0.03%]
严重FXI缺乏症患儿并发脊柱裂
Alperen Kahraman,Merve Yazol,Gülsüm Kayhan et al.
Alperen Kahraman et al.
Ünal Ataş,Fadime Nurcan Alhan,Dilek Beypınar et al.
Ünal Ataş et al.