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Dysplastic versus proliferative CMML – a retrospective analysis of 91 patients from a single institution

Leukemia research, 2001-09, Vol.25 (9), p.741-747

2001

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Myelodysplastic syndromes, from French-American-British to World Health Organization: comparison of classifications on 431 unselected patients from a single institution

Blood, 2001-11, Vol.98 (10), p.2935-2941

2001

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Inactivating mutations and overexpression of BCL10 , a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32)

Nature genetics, 1999-05, Vol.22 (1), p.63-68

1999

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Multiple myeloma : high incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization

Cancer research (Chicago, Ill.), 1995-09, Vol.55 (17), p.3854-3859

1995

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Cross‐validation of prognostic scores in myelodysplastic syndromes on 386 patients from a single institution confirms importance of cytogenetics

British journal of haematology, 1999-08, Vol.106 (2), p.455-463

1999

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Clinicopathogenetic Significance of Chromosomal Abnormalities in Patients With Blastic Peripheral B-Cell Lymphoma

Blood, 1999-11, Vol.94 (9), p.3114-3120

1999

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Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12

British journal of haematology, 1998-03, Vol.100 (3), p.521-533

1998

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Amplification of ribosomal RNA genes in acute myeloid leukemia

Genes chromosomes & cancer, 2001-09, Vol.32 (1), p.11-17

2001

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Karyotype and prognosis in non-Hodgkin lymphoma

Leukemia, 1994-11, Vol.8 (11), p.1929-1939

1994

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Rare occurrence of Philadelphia chromosome negative (but BCR‐ABL positive) CML in a central European population

American journal of hematology, 1994-11, Vol.47 (3), p.253-254

1994

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Drei F lle von Eosinophilenleuk mie mit atypischer Granulation in Eosinophilen und Neutrophilen

Blut, 1976-05, Vol.32 (5), p.337-346

1976

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Cytogenetic Analysis and Fluorescence In Situ Hybridization in a Case of IgD Multiple Myeloma

Cancer genetics and cytogenetics, 1998-09, Vol.105 (2), p.172-176

1998

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Prognostic impact of karyotype and immunologic phenotype in 125 adult patients with de novo AML

Cancer genetics and cytogenetics, 1992-07, Vol.61 (1), p.14-25

1992

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A case of acute lymphoblastic leukemia and throtrast-accumulation

Blut Zeitschrift für die Gesamte Blutforschung, 1975-07, Vol.31 (1), p.5-10

1975

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Is trisomy 22 in acute myeloid leukemia a primary abnormality or only a secondary change associated with inversion 16?

Cancer genetics and cytogenetics, 1989-11, Vol.43 (1), p.119-129

1989

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Dysplastic versus proliferative CMML – a retrospective analysis of 91 patients from a single institution

Myelodysplastic syndromes, from French-American-British to World Health Organization: comparison of classifications on 431 unselected patients from a single institution

Inactivating mutations and overexpression of BCL10 , a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32)

Multiple myeloma : high incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization

Cross‐validation of prognostic scores in myelodysplastic syndromes on 386 patients from a single institution confirms importance of cytogenetics

Clinicopathogenetic Significance of Chromosomal Abnormalities in Patients With Blastic Peripheral B-Cell Lymphoma

Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12

Amplification of ribosomal RNA genes in acute myeloid leukemia

Karyotype and prognosis in non-Hodgkin lymphoma

Rare occurrence of Philadelphia chromosome negative (but BCR‐ABL positive) CML in a central European population

Drei F lle von Eosinophilenleuk mie mit atypischer Granulation in Eosinophilen und Neutrophilen

Cytogenetic Analysis and Fluorescence In Situ Hybridization in a Case of IgD Multiple Myeloma

Prognostic impact of karyotype and immunologic phenotype in 125 adult patients with de novo AML

A case of acute lymphoblastic leukemia and throtrast-accumulation

Is trisomy 22 in acute myeloid leukemia a primary abnormality or only a secondary change associated with inversion 16?

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