Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Nathaniel Wisch"'
Autor:
John Mascarenhas, Nathaniel Wisch, Takefumi Ishii, Wei Zhang, Ying Dai, Mingjiang Xu, Jiapeng Wang, Ronald Hoffman
Publikováno v:
Blood. 113:5942-5950
Pruritus is a common symptom in patients with Philadelphia chromosome–negative myeloproliferative disorders (MPDs). The pathophysiology of MPD-associated pruritus is unclear. We have demonstrated that MPD mast cells (MCs) are involved by the malign
Autor:
Ronald Hoffman, Leonard Issa, John Mascarenhas, Vesna Najfeld, Joseph Tripodi, Manpreet Sidhu, Nathaniel Wisch
Publikováno v:
Cancer genetics. 204(3)
A 65-year-old patient with a high hemoglobin and hematocrit was treated for 14 months with therapeutic phlebotomy when cytogenetics of bone marrow revealed 100% cells with the Ph chromosome and 45% of the Ph+ cells contained trisomy 8. Treatment with
Autor:
Charles J. Parker, Ronald Hoffman, Judith D. Goldberg, Brenda Panzera, Josef T. Prchal, Nathaniel Wisch, John Mascarenhas, Steven Gruenstein, Mingjiang Xu, Amanda LeBlanc, Vesna Najfeld, Xiaoli Wang
Publikováno v:
Experimental hematology. 37(10)
Objective JAK2V617F occurs in ∼93% of patients with polycythemia vera and ∼50% of patients with either primary myelofibrosis or essential thrombocythemia. Chromosomal abnormalities are detected in 50% of patients with primary myelofibrosis, 29% w
Autor:
John Mascarenhas, J Wang, W Zhang, Takefumi Ishii, Zhizhuang Joe Zhao, Selcuk Sozer, Robert S. Hoffman, Mingjiang Xu, Vesna Najfeld, Nathaniel Wisch, Y Dai
Publikováno v:
Leukemia. 23(9)
The Philadelphia chromosome negative myeloproliferative neoplasms (MPNs) are clonal hematologic malignancies frequently characterized by a mutation in JAK2 (JAK2V617F). Peripheral blood (PB) CD34(+) cells from patients with polycythemia vera (PV) and
Autor:
Nathaniel Wisch, Martin Weiner, Lewis R. Silverman, John Crown, Roberto Lipzstein, Michael A. Goldsmith, James F. Holland, Ira Jaffrey, P. Alberto Paciucci, Larry Norton, Seymour Cohen
Publikováno v:
Cancer Investigation. 9:129-132
Out of 16 cases of Merkel cell cancer identified in the records of the Mt. Sinai Medical Center or affiliates, 11 patients developed systemic metastases. Literature review confirms the substantial possibility of dissemination. Both in our series and
Autor:
Jonathan I Warman, Mark R. Fleisher, Felice Mirsky, Burton I. Korelitz, Nathaniel Wisch, Gilbert W Gleim
Publikováno v:
The American journal of gastroenterology. 94(11)
OBJECTIVE: Most complications of 6-mercaptopurine (6MP) used in the treatment of inflammatory bowel disease (IBD) occur early, whereas neoplasms occur late in the course. Concern persists that the risk is increased when 6MP is used. We report our exp
Publikováno v:
Leukemialymphoma. 22(3-4)
A unique patient is reported with longstanding hairy cell leukemia who manifested two distinct abnormalities of factor VIII; factor VIII antibodies and recurrent thrombotic thrombocytopenic purpura (TTP). The patient presented in 1977 with splenomega
Publikováno v:
American journal of hematology. 48(2)
We report two cases of pyroglobulinemia detected in the course of routine determination of fibrinogen levels measured by the heat-precipitation method and that led to the diagnosis of Waldenstrom's macroglobulinemia. The incidence of pyroglobulinemia
Autor:
Joseph Tripodi, Amory Novoselac, Vesna Najfeld, Ronald Hoffman, Nathaniel Wisch, Heike L. Pahl
Publikováno v:
Blood. 116:4110-4110
Abstract 4110 Recurrent chromosomal abnormalities are occurring at the frequency of 45–50% among patients (pts) with primary myelofibrosis (PMF). The prognostic significance of these abnormalities is largely unknown. Among 377 pts (242 from the Mou
Autor:
Wei Zhang, Ying Dai, Takefumi Ishii, John Mascarenhas, Nathaniel Wisch, Jiapeng Wang, Vesna Najfeld, Mingjiang Xu, Ronald Hoffman
Publikováno v:
Blood. 112:3729-3729
The Philadelphia chromosome negative (Ph−) myeloproliferative disorders (MPD), which include polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF) are thought to result from the transformation of a multipotent hemat