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Steven H. Kroft

Researcher at Medical College of Wisconsin

Publications -  152
Citations -  4298

Steven H. Kroft is an academic researcher from Medical College of Wisconsin. The author has contributed to research in topics: Lymphoma & Immunophenotyping. The author has an hindex of 35, co-authored 145 publications receiving 3993 citations. Previous affiliations of Steven H. Kroft include Froedtert Hospital & University of Texas at Dallas.

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Immunophenotypic analysis of hematogones (B-lymphocyte precursors) in 662 consecutive bone marrow specimens by 4-color flow cytometry.

TL;DR: Hematogones always exhibited a typical complex spectrum of antigen expression that defines the normal antigenic evolution of B-cell precursors and lacked aberrant expression, and lymphoblasts in 49 cases of precursor B-ALL showed maturation arrest and exhibited 1 to 11 immunophenotypic aberrancies.
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Zinc-induced copper deficiency: A report of three cases initially recognized on bone marrow examination

TL;DR: The morphologic findings in bone marrow, while not pathognomonic, are sufficiently characteristic to suggest the diagnosis of copper deficiency, leading to further testing to establish the correct diagnosis.
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Precursor B-cell lymphoblastic lymphoma. A study of nine cases lacking blood and bone marrow involvement and review of the literature.

TL;DR: Immunophenotyping revealed a terminal deoxynucleotidyl transferase-positive, immature B-cell population with variable expression of CD10, CD20, and CD45, and Cytogenetic analysis showed additional 21q material as a recurring karyotypic abnormality.
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Presence of simian virus 40 DNA sequences in human lymphomas.

TL;DR: The data suggest that SV40 might be a cofactor in the pathogenesis of non-Hodgkin lymphomas, and is associated previously with some types of human tumours, but not with lymphomas.
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Immunophenotypic analysis of peripheral T-cell neoplasms. A multiparameter flow cytometric approach.

TL;DR: Data indicate that most PTCNs are aberrant by multiparameter flow analysis, however, results must be interpreted within the context of thorough knowledge of the immunophenotypic spectrum of nonneoplastic T cells.