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Risk factors for arterial versus venous thrombosis in polycythemia vera: a single center experience in 587 patients

Blood cancer journal (New York), 2017-12, Vol.7 (12), p.662-662, Article 662

2017

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Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma

Blood cancer journal (New York), 2017-09, Vol.7 (9), p.e600-e600

2017

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Prognostic interaction between ASXL1 and TET2 mutations in chronic myelomonocytic leukemia

Blood cancer journal (New York), 2016-01, Vol.6 (1), p.e385-e385

2016

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European LeukemiaNet-defined primary refractory acute myeloid leukemia: the value of allogeneic hematopoietic stem cell transplant and overall response

Blood cancer journal (New York), 2022-01, Vol.12 (1), p.7-8, Article 7

2022

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Core-binding factor acute myeloid leukemia: long-term outcome of 70 patients uniformly treated with "7+3"

Blood cancer journal (New York), 2022-04, Vol.12 (4), p.55-55, Article 55

2022

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Prognostic relevance of lymphocytopenia, monocytopenia and lymphocyte-to-monocyte ratio in primary myelodysplastic syndromes: a single center experience in 889 patients

Blood cancer journal (New York), 2017-03, Vol.7 (3), p.e550-e550

2017

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Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Blood cancer journal (New York), 2016-04, Vol.6 (4), p.e414-e414

2016

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Failure of front-line autologous transplant in anaplastic lymphoma kinase-positive diffuse large B-cell lymphoma

Bone marrow transplantation (Basingstoke), 2011-06, Vol.46 (6), p.904-905

2011

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Flow cytometry based monocyte subset analysis accurately distinguishes chronic myelomonocytic leukemia from myeloproliferative neoplasms with associated monocytosis

Blood cancer journal (New York), 2017-07, Vol.7 (7), p.e584-e584

2017

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Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature

Journal of medical genetics, 2006-02, Vol.43 (2), p.e08-e08

2006

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Prognostic impact of bone marrow fibrosis in polycythemia vera: validation of the IWG-MRT study and additional observations

Blood cancer journal (New York), 2017-03, Vol.7 (3), p.e538-e538

2017

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Abnormal FISH in patients with immunoglobulin light chain amyloidosis is a risk factor for cardiac involvement and for death

Blood cancer journal (New York), 2015-05, Vol.5 (5), p.e310-e310

2015

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Novel recurrent mutations in ethanolamine kinase 1 (ETNK1) gene in systemic mastocytosis with eosinophilia and chronic myelomonocytic leukemia

Blood cancer journal (New York), 2015-01, Vol.5 (1), p.e275-e275

2015

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Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Blood cancer journal (New York), 2015-01, Vol.5 (1), p.e270-e270

2015

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Occurrence and prognostic significance of cytogenetic evolution in patients with multiple myeloma

Blood cancer journal (New York), 2016-03, Vol.6 (3), p.e401-e401

2016

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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

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Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Blood cancer journal (New York), 2016-04, Vol.6 (4), p.e415-e415

2016

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Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Blood cancer journal (New York), 2015-02, Vol.5 (2), p.e280-e280

2015

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Liver function test abnormalities and their clinical relevance in primary myelofibrosis

Blood cancer journal (New York), 2017-04, Vol.7 (4), p.e557-e557

2017

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Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Blood cancer journal (New York), 2016-05, Vol.6 (5), p.e416-e416

2016

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Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

Human molecular genetics, 1994-07, Vol.3 (7), p.1035-1039

1994

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Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course

Blood cancer journal (New York), 2014-10, Vol.4 (10), p.e253-e253

2014

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Germline origins in the human F9 gene : frequent G:C→A:T mosaicism and increased mutations with advanced maternal age

Human genetics, 1999-12, Vol.105 (6), p.629-640

1999

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Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

American journal of clinical pathology, 2021-10, Vol.156 (Supplement_1), p.S100-S101

2021

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The factor IX gene as a model for analysis of human germline mutations: an update

Human molecular genetics, 1996-01, Vol.5 (Supplement-1), p.1505-1514

1996

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Risk factors for arterial versus venous thrombosis in polycythemia vera: a single center experience in 587 patients

Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma

Prognostic interaction between ASXL1 and TET2 mutations in chronic myelomonocytic leukemia

European LeukemiaNet-defined primary refractory acute myeloid leukemia: the value of allogeneic hematopoietic stem cell transplant and overall response

Core-binding factor acute myeloid leukemia: long-term outcome of 70 patients uniformly treated with "7+3"

Prognostic relevance of lymphocytopenia, monocytopenia and lymphocyte-to-monocyte ratio in primary myelodysplastic syndromes: a single center experience in 889 patients

Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Failure of front-line autologous transplant in anaplastic lymphoma kinase-positive diffuse large B-cell lymphoma

Flow cytometry based monocyte subset analysis accurately distinguishes chronic myelomonocytic leukemia from myeloproliferative neoplasms with associated monocytosis

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature

Prognostic impact of bone marrow fibrosis in polycythemia vera: validation of the IWG-MRT study and additional observations

Abnormal FISH in patients with immunoglobulin light chain amyloidosis is a risk factor for cardiac involvement and for death

Novel recurrent mutations in ethanolamine kinase 1 (ETNK1) gene in systemic mastocytosis with eosinophilia and chronic myelomonocytic leukemia

Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Occurrence and prognostic significance of cytogenetic evolution in patients with multiple myeloma

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

Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Liver function test abnormalities and their clinical relevance in primary myelofibrosis

Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course

Germline origins in the human F9 gene : frequent G:C→A:T mosaicism and increased mutations with advanced maternal age

Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

The factor IX gene as a model for analysis of human germline mutations: an update

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