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Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma

Leukemia, 2003-02, Vol.17 (2), p.427-436

2003

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JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained

Leukemia, 2006-06, Vol.20 (6), p.971-978

2006

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Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1

Leukemia, 2004-01, Vol.18 (1), p.156-160

2004

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B-CLL cells are capable of synthesis and secretion of both pro- and anti-angiogenic molecules

Leukemia, 2002-05, Vol.16 (5), p.911-919

2002

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Diagnostic utility of fluorescence in situ hybridization in mantle‐cell lymphoma

British journal of haematology, 2000-09, Vol.110 (4), p.856-862

2000

Volltextzugriff (PDF)

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia

British journal of haematology, 2005-07, Vol.130 (1), p.36-42

2005

Volltextzugriff (PDF)

WHO-defined chronic neutrophilic leukemia: a long-term analysis of 12 cases and a critical review of the literature

Leukemia, 2005-02, Vol.19 (2), p.313-317

2005

Volltextzugriff (PDF)

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma

Bone marrow transplantation (Basingstoke), 2003-08, Vol.32 (3), p.317-324

2003

Volltextzugriff (PDF)

Abnormal Function of the Bone Marrow Microenvironment in Chronic Myelogenous Leukemia: Role of Malignant Stromal Macrophages

Blood, 1995-06, Vol.85 (12), p.3636-3645

1995

Volltextzugriff (PDF)

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5q

Leukemia, 2009-04, Vol.23 (4), p.796-800

2009

Volltextzugriff (PDF)

Chronic neutrophilic leukemia (CNL): a clinical, pathologic and cytogenetic study

Leukemia, 2001, Vol.15 (1), p.35-40

2001

Volltextzugriff (PDF)

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

British journal of haematology, 1999-08, Vol.106 (2), p.445-454

1999

Volltextzugriff (PDF)

The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study

American journal of clinical pathology, 2000-06, Vol.113 (6), p.831-837

2000

Volltextzugriff (PDF)

FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature

Leukemia research, 2006-08, Vol.30 (8), p.965-970

2006

Volltextzugriff (PDF)

Long-term survival of patients with acute myeloid leukemia: A third follow-up of the Fourth International Workshop on Chromosomes in Leukemia

Cancer, 1997-12, Vol.80 (11), p.2191-2198

1997

Volltextzugriff (PDF)

The 5q- Syndrome: A Single-Institution Study of 43 Consecutive Patients

Blood, 1993-02, Vol.81 (4), p.1040-1045

1993

Volltextzugriff (PDF)

Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia

British journal of haematology, 2001-06, Vol.113 (3), p.763-771

2001

Volltextzugriff (PDF)

The Clinical Significance of Cytogenetic Studies in 100 Patients With Multiple Myeloma, Plasma Cell Leukemia, or Amyloidosis

Blood, 1985-08, Vol.66 (2), p.380-390

1985

Volltextzugriff (PDF)

Agnogenic myeloid metaplasia associated with Klinefelter syndrome: a case report

Annals of hematology, 2002-04, Vol.81 (4), p.215-218

2002

Volltextzugriff (PDF)

Analysis of clonal B‐cell CD38 and immunoglobulin variable region sequence status in relation to clinical outcome for B‐chronic lymphocytic leukaemia

British journal of haematology, 2001-12, Vol.115 (4), p.854-861

2001

Volltextzugriff (PDF)

True T-Cell Chronic Lymphocytic Leukemia: A Morphologic and Immunophenotypic Study of 25 Cases

Blood, 1995-08, Vol.86 (3), p.1163-1169

1995

Volltextzugriff (PDF)

Chromosome abnormalities in the myeloproliferative disorders

Seminars in oncology, 1995-08, Vol.22 (4), p.341

1995

Volltextzugriff (PDF)

Chromosomal abnormalities in systemic amyloidosis

British journal of haematology, 1998-12, Vol.103 (3), p.704-710

1998

Volltextzugriff (PDF)

Hematologic disorders associated with deletions of chromosome 20q : A clinicopathologic study of 107 patients

American journal of clinical pathology, 1996-11, Vol.106 (5), p.680-688

1996

Volltextzugriff (PDF)

Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia

Blood, 1998-05, Vol.91 (9), p.3357-3365

1998

Volltextzugriff (PDF)

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Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained

Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1

B-CLL cells are capable of synthesis and secretion of both pro- and anti-angiogenic molecules

Diagnostic utility of fluorescence in situ hybridization in mantle‐cell lymphoma

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia

WHO-defined chronic neutrophilic leukemia: a long-term analysis of 12 cases and a critical review of the literature

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma

Abnormal Function of the Bone Marrow Microenvironment in Chronic Myelogenous Leukemia: Role of Malignant Stromal Macrophages

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5q

Chronic neutrophilic leukemia (CNL): a clinical, pathologic and cytogenetic study

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study

FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature

Long-term survival of patients with acute myeloid leukemia: A third follow-up of the Fourth International Workshop on Chromosomes in Leukemia

The 5q- Syndrome: A Single-Institution Study of 43 Consecutive Patients

Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia

The Clinical Significance of Cytogenetic Studies in 100 Patients With Multiple Myeloma, Plasma Cell Leukemia, or Amyloidosis

Agnogenic myeloid metaplasia associated with Klinefelter syndrome: a case report

Analysis of clonal B‐cell CD38 and immunoglobulin variable region sequence status in relation to clinical outcome for B‐chronic lymphocytic leukaemia

True T-Cell Chronic Lymphocytic Leukemia: A Morphologic and Immunophenotypic Study of 25 Cases

Chromosome abnormalities in the myeloproliferative disorders

Chromosomal abnormalities in systemic amyloidosis

Hematologic disorders associated with deletions of chromosome 20q : A clinicopathologic study of 107 patients

Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia

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