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Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene

British journal of haematology, 1999-11, Vol.107 (2), p.310-316

1999

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Long‐term efficacy of first‐line ibrutinib treatment for chronic lymphocytic leukaemia in patients with TP53 aberrations: a pooled analysis from four clinical trials

British journal of haematology, 2022-02, Vol.196 (4), p.947-953

2022

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Long‐term efficacy of first‐line ibrutinib treatment for chronic lymphocytic leukaemia in patients with TP53 aberrations: apooled analysis from four clinical trials

British journal of haematology, 2022-02, Vol.196 (4), p.947-953

2022

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Cardiac toxicity in a pilot study of duvelisib and ibrutinib combination therapy for chronic lymphocytic leukaemia

British journal of haematology, 2023-01, Vol.200 (2), p.261-263

2023

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Genomic evolution of ibrutinib‐resistant clones in Waldenström macroglobulinaemia

British journal of haematology, 2020-06, Vol.189 (6), p.1165-1170

2020

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Genomic Evolution of Ibrutinib Resistant Clones in Waldenström Macroglobulinemia

British journal of haematology, 2020-02, Vol.189 (6), p.1165-1170

2020

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Flow cytometry for ZAP‐70: New colors for chronic lymphocytic leukemia

Cytometry. Part B, Clinical cytometry, 2006-07, Vol.70B (4), p.201-203

Wiestner, Adrian

2006

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A phase II study of ibrutinib and short‐course fludarabine in previously untreated patients with chronic lymphocytic leukemia

American journal of hematology, 2020-11, Vol.95 (11), p.E310-E313

2020

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Inflammation, TNFα and endothelial dysfunction link lenalidomide to venous thrombosis in chronic lymphocytic leukemia

American journal of hematology, 2011-10, Vol.86 (10), p.835-840

2011

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Unexpected detection of monoclonal B‐cell lymphocytosis in a HLA‐matched sibling donor on the day of allogeneic stem cell transplantation for a patient with chronic lymphocytic leukaemia: clinical outcome

British journal of haematology, 2010-06, Vol.149 (6), p.905-907

2010

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Inflammation, TNF[alpha] and endothelial dysfunction link lenalidomide to venous thrombosis in chronic lymphocytic leukemia

American journal of hematology, 2011-10, Vol.86 (10), p.835

2011

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The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non-familial essential thrombocythaemia

British journal of haematology, 1998-09, Vol.102 (5), p.1341-1343

1998

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Bcl‐2 level as a biomarker for 13q14 deletion in CLL

Cytometry. Part B, Clinical cytometry, 2013-07, Vol.84B (4), p.237-247

2013

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Improved ZAP-70 Assay Using Two Clones and Multiple Methods of Analysis

Cytometry. Part B, Clinical cytometry, 2011-04, Vol.80 (5), p.309-317

2011

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Methodological comparison of two anti‐ZAP‐70 antibodies

Cytometry. Part B, Clinical cytometry, 2011-09, Vol.80B (5), p.300-308

2011

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Improved ZAP‐70 assay using two clones, multiple methods of analysis and clinical correlation

Cytometry. Part B, Clinical cytometry, 2011-09, Vol.80B (5), p.309-317

2011

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Combined normal donor and CLL: Single tube ZAP‐70 analysis

Cytometry. Part B, Clinical cytometry, 2012-03, Vol.82B (2), p.67-77

2012

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Immunophenotypic features distinguishing familial chronic lymphocytic leukemia from sporadic chronic lymphocytic leukemia

Cytometry. Part B, Clinical cytometry, 2008-07, Vol.74B (4), p.221-226

2008

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The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non‐familial essential thrombocythaemia

British journal of haematology, 1998-09, Vol.102 (5), p.1341-1343

1998

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Howell Jolly bodies and a history of home‐made bread

British journal of haematology, 2001-08, Vol.114 (2), p.247-247

2001

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The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with nonafamilial essential thrombocythaemia

British journal of haematology, 1998-08, Vol.102 (5), p.00-00

1998

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Unexpected detection of monoclonal B-cell lymphocytosis in a HLA-matched sibling donor on the day of allogeneic stem cell transplantation for a patient with chronic lymphocytic leukaemia: clinical outcome

British journal of haematology, 2010, Vol.149 (6), p.905-907

2010

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Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene

Long‐term efficacy of first‐line ibrutinib treatment for chronic lymphocytic leukaemia in patients with TP53 aberrations: a pooled analysis from four clinical trials

Long‐term efficacy of first‐line ibrutinib treatment for chronic lymphocytic leukaemia in patients with TP53 aberrations: apooled analysis from four clinical trials

Cardiac toxicity in a pilot study of duvelisib and ibrutinib combination therapy for chronic lymphocytic leukaemia

Genomic evolution of ibrutinib‐resistant clones in Waldenström macroglobulinaemia

Genomic Evolution of Ibrutinib Resistant Clones in Waldenström Macroglobulinemia

Flow cytometry for ZAP‐70: New colors for chronic lymphocytic leukemia

A phase II study of ibrutinib and short‐course fludarabine in previously untreated patients with chronic lymphocytic leukemia

Inflammation, TNFα and endothelial dysfunction link lenalidomide to venous thrombosis in chronic lymphocytic leukemia

Unexpected detection of monoclonal B‐cell lymphocytosis in a HLA‐matched sibling donor on the day of allogeneic stem cell transplantation for a patient with chronic lymphocytic leukaemia: clinical outcome

Inflammation, TNF[alpha] and endothelial dysfunction link lenalidomide to venous thrombosis in chronic lymphocytic leukemia

The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non-familial essential thrombocythaemia

Bcl‐2 level as a biomarker for 13q14 deletion in CLL

Improved ZAP-70 Assay Using Two Clones and Multiple Methods of Analysis

Methodological comparison of two anti‐ZAP‐70 antibodies

Improved ZAP‐70 assay using two clones, multiple methods of analysis and clinical correlation

Combined normal donor and CLL: Single tube ZAP‐70 analysis

Immunophenotypic features distinguishing familial chronic lymphocytic leukemia from sporadic chronic lymphocytic leukemia

The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non‐familial essential thrombocythaemia

Howell Jolly bodies and a history of home‐made bread

The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with nonafamilial essential thrombocythaemia

Unexpected detection of monoclonal B-cell lymphocytosis in a HLA-matched sibling donor on the day of allogeneic stem cell transplantation for a patient with chronic lymphocytic leukaemia: clinical outcome

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