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Two rare pathogenic HBB variants in a patient with β-thalassemia intermedia
(2020)
The β-thalassemias are a group of hereditary disorders with autosomal recessive inheritance characterized by the presence of defective synthesis of the β-globin chain, an integral component of the hemoglobin molecule, ...
Stem cell transplantation for high-risk acute lymphoblastic leukemia in a developing country: A single-center experience
(Wiley, 2020)
[No abstract available]
Invasive saprochaete capitata infection in a patient with autosomal recessive CARD9 deficiency and a review of the literature
(Springer/Plenum Publishers, 2020)
Purpose Autosomal recessive (AR) CARD9 deficiency is an inherited immune disorder which results in impaired innate immunity against various fungi. Superficial and invasive fungal infections, mainly caused by Candida or ...
Are the anxiety levels of pediatric hematology-oncology patients different from healthy peers during the COVID-19 outbreak?
(Lippincott Williams and Wilkins, 2020)
The COVID-19 outbreak has caused anxiety among children with hematology-oncology disease and their families, as it has in every segment of society. In this study, we aimed to detect the anxiety levels of children with ...
Biallelic form of a known CD3E mutation in a patient with severe combined immunodeficiency
(Springer/Plenum Publishers, 2020)
To the Editor: T cell receptor (TCR) complex consists of αβ or γδ TCR chains in combination with four CD3 subunits, CD3ε, CD3γ, CD3δ, and CDζ [1]. This complex is required for thymocyte development and the initiation of T ...
