Zobrazeno 1 - 10
of 35
pro vyhledávání: '"G W, Dewald"'
Publikováno v:
Mayo Clinic Proceedings. 73:132-137
Publikováno v:
Mayo Clinic Proceedings. 71:643-648
Autor:
D F, Jelinek, R C, Tschumper, S M, Geyer, N D, Bone, G W, Dewald, C A, Hanson, M J, Stenson, T E, Witzig, A, Tefferi, N E, Kay
Publikováno v:
British journal of haematology. 115(4)
Recent reports suggest that the expression of germline (GL) Ig variable region heavy-chain genes (VH) is a negative prognostic factor for B-cell chronic lymphocytic leukaemia (B-CLL) patients and that CLL B-cell CD38 expression may be a surrogate mar
Autor:
J M, Bennett, M S, Young, J L, Liesveld, E, Paietta, K B, Miller, H M, Lazarus, R D, Marsh, W R, Friedenberg, H T, Saba, F A, Hayes, G W, Dewald, W, Hiddemann, J M, Rowe
Publikováno v:
American journal of hematology. 66(1)
A Phase II study of GM-CSF with intermediate-dose cytarabine and mitoxantrone was conducted in patients with high-risk myelodysplastic syndrome. It was designed to evaluate if priming with growth factor could increase the efficiency of chemotherapy.
Publikováno v:
British journal of haematology. 113(3)
The prognostic significance of bone marrow cytogenetic lesions in myelofibrosis with myeloid metaplasia (MMM) was investigated in a retrospective series of 165 patients. An abnormal karyotype was demonstrated in 57% of patients. At diagnosis (n = 92)
Autor:
D M, Menke, G W, DeWald
Publikováno v:
Southern medical journal. 94(5)
Castleman's disease (CD) is a distinctive type of atypical lymph node hyperplasia that is often clonal. In a previously reported series of CD, clonal populations of plasma cells were detected by immunohistology in 4 of 39 cases (10%, lambda restricte
Autor:
E D, Remstein, P J, Kurtin, I, Buño, R J, Bailey, J, Proffitt, W A, Wyatt, C A, Hanson, G W, Dewald
Publikováno v:
British journal of haematology. 110(4)
Mantle-cell lymphoma (MCL) has a poorer prognosis than other small B-cell lymphomas, thus a definitive diagnosis is essential. The t(11;14)(q13;q32) associated with MCL juxtaposes portions of CCND1 (11q13) and IGH (14q32), resulting in over-expressio
Publikováno v:
American journal of clinical pathology. 113(6)
We identified 24 cases of multiple myeloma with the t(11;14)(q13;q32). In 22 cases, the t(11;14)(q13;q32) was part of a complex karyotype, and in 2 cases it was an isolated abnormality. All patients had clinical and laboratory features consistent wit
Publikováno v:
British journal of haematology. 106(2)
A clinicopathologic study was performed on 15 patients with haematological malignancies in which isochromosome 17q [i(17q)] was the sole structural chromosome abnormality identified in bone marrow. The data indicated that an isolated i(17q) is associ
Autor:
R, Fonseca, G J, Ahmann, S M, Jalal, G W, Dewald, D R, Larson, T M, Therneau, M A, Gertz, R A, Kyle, P R, Greipp
Publikováno v:
British journal of haematology. 103(3)
Primary systemic amyloidosis (AL) is a plasma cell disorder characterized by deposition of monoclonal light chains in different organ systems. Although multiple and complex numerical chromosomal abnormalities have been described in patients with mult