CLINICAL CORRELATIONS AND MOLECULAR ANALYSIS OF HUMAN CYTOMEGALOVIRUS (HCMV) INFECTION IN BRAZILIAN PATIENTS WITH SICKLE CELL DISEASE, BETA-THALASSEMIA MAJOR, AND BLOOD DONORS

被引：0
|
作者：
Nanev Slavov, S. [1 ]
Kashima, S. [1 ]
de Deus Wagatsuma, V. [1 ]
Silva-Pinto, A. [1 ]
Covas, D. [2 ]
机构：
[1] Hemoctr Ribierao, Ribeirao Preto, Brazil
[2] Fac Med Ribeirao Preto, Dept Clin Med, Ribeirao Preto, Brazil
来源：
HAEMATOLOGICA | 2013年 / 98卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P430
引用
收藏
页码：182 / 182
页数：1
相关论文
共 50 条
  • [31] Cytokine dependent hematopoietic cell linker (CLNK) is highly elevated in blood transfusion dependent beta-thalassemia major patients
    Al-Hakeim, H. K.
    Al-Mayali, H. H.
    Moustafa, S. R.
    Maes, M.
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2021, 28 (02) : 194 - 198
  • [32] Comparison of serology and molecular detection of common red cell antigens in multitransfused thalassemia major and sickle cell disease patients
    Shah, Avani
    Patel, Parizad
    Patel, Keyur
    Patel, Binal
    Jariwala, Keyuri
    Sharma, Preeti
    Mishra, Kanchan
    Ghosh, Kanjaksha
    TRANSFUSION AND APHERESIS SCIENCE, 2020, 59 (01)
  • [33] QUANTITATIVE CHANGES OF RED BLOOD-CELL SHAPES IN RELATION TO CLINICAL-FEATURES IN BETA-THALASSEMIA HBE DISEASE
    BUNYARATVEJ, A
    SAHAPHONG, S
    BHAMARAPRAVATI, N
    WASI, P
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1985, 83 (05) : 555 - 559
  • [34] A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta-Thalassemia and Sickle Cell Disease
    Bai, Hao
    Cai, Liuhong
    Machairaki, Vasiliki
    Gao, Yongxing
    Ye, Zhaohui
    Cheng, Linzhao
    BLOOD, 2017, 130
  • [35] A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta-Thalassemia and Sickle Cell Disease
    Cai, Liuhong
    Bai, Hao
    Mahairaki, Vasiliki
    Gao, Yongxing
    He, Chaoxia
    Wen, Yanfei
    Jin, You-Chuan
    Wang, You
    Pan, Rachel L.
    Qasba, Armaan
    Ye, Zhaohui
    Cheng, Linzhao
    STEM CELLS TRANSLATIONAL MEDICINE, 2018, 7 (01) : 87 - 97
  • [36] Clinical Outcomes of Molecular Matching in Transfusion-Dependent Patients with Sickle Cell Disease (SCD) and Thalassemia
    de Macedo, Mayra Dorigan
    dos Santos, Tamires Delfino
    Perecin Menegati, Sheila Fatima
    Pereira, Fabricio Biscaro
    Gilli, Simone
    Castilho, Lilian
    TRANSFUSION, 2017, 57 : 137A - 138A
  • [37] Spectral domain optical coherence tomography findings in Turkish sickle-cell disease and beta thalassemia major patients
    Ulusoy, Mahmut Oguz
    Turk, Hakan
    Kivanc, Sertac Argun
    JOURNAL OF CURRENT OPHTHALMOLOGY, 2019, 31 (03): : 275 - 280
  • [38] Genetic Modifiers of Hemoglobin Expression from a Clinical Perspective in Hemoglobinopathy Patients with Beta Thalassemia and Sickle Cell Disease
    Diamantidis, Michael D.
    Ikonomou, Georgia
    Argyrakouli, Ioanna
    Pantelidou, Despoina
    Delicou, Sophia
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (22)
  • [39] Clinical significance of qualitative human cytomegalovirus (HCMV) detection in cell-free serum samples in HIV-infected patients at risk for HCMV disease
    Laue, T
    Mertenskotter, T
    Grewing, T
    Degen, O
    vanLunzen, J
    Dietrich, M
    Schmitz, H
    AIDS, 1997, 11 (09) : 1195 - 1196
  • [40] Outcome of Patients with Beta-Thalassemia Major Given Either Bone Marrow and Frozen Cord Blood of Same Sibling or Bone Marrow Transplantation from Sibling Donors
    Wu, Xuedong
    Wen, Jianyun
    Pei Fuyu
    Chen, Libai
    Liao, Jianyun
    He, Yuelin
    Li, Qi
    Ruan, Yongsheng
    Li, Chunfu
    BLOOD, 2014, 124 (21)
12345