Co-Authors
                            
                            
                                This is a "connection" page, showing publications co-authored by   MOHAMED ELGHETANY   and   ANDREA MARCOGLIESE.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            1.469
         
        
        
     
 
    
        
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            Inherited Bone Marrow Failure Syndromes: Biology and Diagnostic Clues. Clin Lab Med. 2021 09; 41(3):417-431.
            
            
                Score: 0.741
             
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            Infantile Pyknocytosis Revisited: Possible Familial Trend in a Study of 9 Patients. Arch Pathol Lab Med. 2025 Jul 08.
            
            
                Score: 0.245
             
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            Are micromegakaryocytes specific for refractory cytopenia of childhood (RCC)? A study of 38 pediatric patients with thrombocytopenia unrelated to RCC. Leuk Res. 2016 08; 47:84-7.
            
            
                Score: 0.130
             
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            Childhood and Adolescent Relapsed/Refractory Aggressive B-Cell Lymphomas With t(8;14) and BCL2 Expression, Burkitt Lymphoma Versus Diffuse Large B-Cell Lymphoma: A Diagnostic Challenge. Pediatr Dev Pathol. 2024 Jul-Aug; 27(4):348-353.
            
            
                Score: 0.056
             
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            Frequent detection of CBFA2T3::GLIS2 fusion and RAM-phenotype in pediatric non-Down syndrome acute megakaryoblastic leukemia: a possible novel relationship with aberrant cytoplasmic CD3 expression. Leuk Lymphoma. 2023 02; 64(2):462-467.
            
            
                Score: 0.051
             
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            The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic?Neoplasms. Leukemia. 2022 07; 36(7):1703-1719.
            
            
                Score: 0.050
             
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            A Case of a Very Young Child With T Lymphoblastic Lymphoma With Eosinophilia and PDGFRB Translocation: A Rare Form of Myeloid/Lymphoid Neoplasm Associated With Eosinophilia and Rearrangements of PDGFRA, PDGFRB or FGFR1. Clin Lymphoma Myeloma Leuk. 2020 12; 20(12):e990-e993.
            
            
                Score: 0.044
             
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            Pediatric myeloid sarcoma: a single institution clinicopathologic and molecular analysis. Pediatr Hematol Oncol. 2020 Feb; 37(1):76-89.
            
            
                Score: 0.041
             
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            A clinicopathologic study of the spectrum of systemic forms of EBV-associated T-cell lymphoproliferative disorders of childhood: A single tertiary care pediatric institution experience in North America. Pediatr Blood Cancer. 2019 08; 66(8):e27798.
            
            
                Score: 0.040
             
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            Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN. Blood. 2018 08 09; 132(6):658-662.
            
            
                Score: 0.037
             
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            Standardized high-sensitivity flow cytometry testing for paroxysmal nocturnal hemoglobinuria in children with acquired bone marrow failure disorders: A single center US study. Cytometry B Clin Cytom. 2018 07; 94(4):699-704.
            
            
                Score: 0.035