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Akademický článek

A Case of Acute Eosinophilic Leukemia with a Novel PHF6 Mutation

Autor: J. J. Lipof, E. J. Huselton, C. S. Zent, A. Evans, B. Zhang, P. G. Rothberg, J. M. Bennett

Publikováno v: Case Reports in Hematology, Vol 2021 (2021)

Acute eosinophilic leukemia (AEL) is a rare form of acute myeloid leukemia (AML) that requires prompt exclusion of reactive etiologies of eosinophilia and identification of an underlying acute myeloid neoplasm. Myeloid neoplasms with prominent eosino

Externí odkaz: https://doaj.org/article/d93bfee01b3f4e35913535be554e6d9b

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Chronic lymphocytic leukemia incidence is substantially higher than estimated from tumor registry data

Autor: C S, Zent, M J, Kyasa, R, Evans, S A, Schichman

Publikováno v: Cancer. 92(5)

Although chronic lymphocytic leukemia (CLL) often is described as the most common leukemia in the U.S. and Western Europe, to the authors' knowledge the true incidence of CLL in the U.S. is unknown. CLL incidence is estimated from tumor registry repo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cf7b8f5cda89d10cd4990e2168dd5191
https://pubmed.ncbi.nlm.nih.gov/11571749

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Use of HFE mutation analysis for hereditary hemochromatosis: the need for physician education in the translation of basic science to clinical practice

Autor: M, Kohli, S A, Schichman, L, Fink, C S, Zent

Publikováno v: Southern medical journal. 93(5)

Hereditary hemochromatosis (HH) is a common hereditary disorder of iron metabolism causing iron overload, organ failure, and malignancy. Preclinical diagnosis using HFE gene analysis followed by prophylactic phlebotomy can completely prevent the dise

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::61ca1556024b0298f986257ed5496696
https://pubmed.ncbi.nlm.nih.gov/10832943

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Relationship between megakaryocyte mass and serum thrombopoietin levels as revealed by a case of cyclic amegakaryocytic thrombocytopenic purpura

Autor: C S, Zent, J, Ratajczak, M Z, Ratajczak, J, Anastasi, P C, Hoffman, A M, Gewirtz

Publikováno v: British journal of haematology. 105(2)

Cyclic amegakaryocytic thrombocytopenic purpura is a rare syndrome characterized by periodic failure of megakaryocytopoiesis. In this report we describe a patient with cyclic amegakaryocytic thrombocytopenic purpura associated with a megakaryocyte sp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3026a0830c0207fe6d9274a8e229de54
https://pubmed.ncbi.nlm.nih.gov/10233421

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Oligoclonal protein bands and Ig isotype switching in multiple myeloma treated with high-dose therapy and hematopoietic cell transplantation

Autor: C S, Zent, C S, Wilson, G, Tricot, S, Jagannath, D, Siegel, K R, Desikan, N, Munshi, D, Bracy, B, Barlogie, A W, Butch

Publikováno v: Blood. 91(9)

Multiple myeloma (MM) is usually characterized by production of a single serum monoclonal protein of constant isotype and light-chain restriction. Multiple Ig isotypes and isotype switches, which are rare in untreated patients, are reported to be mor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a6509f09d50e546f80413b43d21bf13d
https://pubmed.ncbi.nlm.nih.gov/9558413

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Prediction of amikacin dose requirements in neutropenic patients with haematological disease

Autor: C S, Zent, R, Allin, P I, Folb

Publikováno v: South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde. 83(11)

This study reports on the use of an easily applied Bayesian forecasting programme (OPT; Clydesoft) to predict amikacin dose requirements in 10 patients with haematological disease and neutropenic fever. OPT-determined dose adjustment achieved therape

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::298740d46733144dde34c27a4d5bfc0a
https://pubmed.ncbi.nlm.nih.gov/7839219

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