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ANDREA MARCOGLIESE to Child

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This is a "connection" page, showing publications ANDREA MARCOGLIESE has written about Child.
ANDREA MARCOGLIESE
Connection Strength
0.189
Child
  1. CD123 Immunohistochemical Expression Is a Specific But Insensitive Marker of Early T-precursor Leukemia. Appl Immunohistochem Mol Morphol. 2016 Jan; 24(1):e4-5.
    View in: PubMed
    Score: 0.028
  2. Disordered differentiation and cellular senescence in pediatric Hodgkin Reed-Sternberg cells. Blood Adv. 2026 Apr 28; 10(8):2711-2726.
    View in: PubMed
    Score: 0.014
  3. Co-Occurrence of ETV6::RUNX1 and P2RY8::CRLF2 Fusion in a Patient with Relapsed Acute B Lymphoblastic Leukemia. Ann Clin Lab Sci. 2025 Jan; 55(1):133-141.
    View in: PubMed
    Score: 0.013
  4. 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.
    View in: PubMed
    Score: 0.012
  5. Unique Hemoglobinopathy Pattern Following Treatment with Voxelotor. Ann Clin Lab Sci. 2023 Jul; 53(4):647-652.
    View in: PubMed
    Score: 0.012
  6. Programmed cell death ligand 1 expression in aggressive pediatric non-Hodgkin lymphomas: frequency, genetic mechanisms, and clinical significance. Haematologica. 2022 08 01; 107(8):1880-1890.
    View in: PubMed
    Score: 0.011
  7. Childhood lymphomatoid papulosis Type D, a rare and challenging diagnosis. Pediatr Dermatol. 2022 Nov; 39(6):943-945.
    View in: PubMed
    Score: 0.011
  8. Near-Haploid B-Cell Acute Lymphoblastic Leukemia in a Patient with Rubinstein-Taybi Syndrome. Pediatr Hematol Oncol. 2022 Nov; 39(8):747-754.
    View in: PubMed
    Score: 0.011
  9. Acute myeloid leukemia in a child with familial platelet disorder and a cryptic runx1 intragenic deletion. Pediatr Hematol Oncol. 2022 09; 39(6):580-585.
    View in: PubMed
    Score: 0.011
  10. Philadelphia chromosome-positive pre-B lymphoblastic leukemia presenting as acute hepatic failure in a pediatric patient. Pediatr Hematol Oncol. 2022 08; 39(5):481-487.
    View in: PubMed
    Score: 0.011
  11. Pediatric myeloid sarcoma: a single institution clinicopathologic and molecular analysis. Pediatr Hematol Oncol. 2020 Feb; 37(1):76-89.
    View in: PubMed
    Score: 0.009
  12. 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.
    View in: PubMed
    Score: 0.009
  13. PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome: A rare cause of childhood neutropenia associated with systemic inflammation and hyperzincemia. Pediatr Blood Cancer. 2019 01; 66(1):e27439.
    View in: PubMed
    Score: 0.008
  14. Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN. Blood. 2018 08 09; 132(6):658-662.
    View in: PubMed
    Score: 0.008
  15. 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.
    View in: PubMed
    Score: 0.008
  16. 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.
    View in: PubMed
    Score: 0.007
  17. Secondary Bone Marrow Fibrosis in Children And Young Adults: An Institutional Experience. J Pediatr Hematol Oncol. 2016 Mar; 38(2):97-101.
    View in: PubMed
    Score: 0.007
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.