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FAMILIAL GIANT HYPERPLASTIC POLYPOSIS PREDISPOSING TO COLORECTAL CANCER: A NEW HEREDITARY BOWEL CANCER SYNDROME

The Journal of pathology, 1996-05, Vol.179 (1), p.20-25

1996

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P687: A PHASE 1 STUDY WITH THE NOVEL B‐CELL LYMPHOMA 2 (BCL2) INHIBITOR BGB‐11417 AS MONOTHERAPY OR IN COMBINATION WITH ZANUBRUTINIB (ZANU) IN PATIENTS (PTS) WITH B‐CELL MALIGNANCIES: PRELIMINARY DATA

HemaSphere, 2022-06, Vol.6, p.583-584

2022

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Diagnostic use of microsatellite instability in hereditary non-polyposis colorectal cancer

The Lancet (British edition), 1995-11, Vol.346 (8984), p.1200-1201

1995

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Factor IX polypyrimidine tract mutation analysis using mRNA from peripheral blood leukocytes

Journal of thrombosis and haemostasis, 2004-11, Vol.2 (11), p.2073-2075

2004

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The endothelial protein C receptor (EPCR) 23bp insert in patients with myocardial infarction

Thrombosis and haemostasis, 2001-04, Vol.85 (4), p.749-751

2001

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Prevalence of factor v leiden and prothrombin variant g20210a in patients age <50 years with no significant stenoses at angiography three to four weeks after myocardial infarction

Journal of the American College of Cardiology, 2000-09, Vol.36 (3), p.717-722

2000

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Colorectal neoplasms detected colonoscopically in at-risk members of colorectal cancer families stratified by the demonstration of DNA microsatellite instability

Journal of molecular medicine (Berlin, Germany), 1996-09, Vol.74 (9), p.547-551

1996

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Analysis of ras gene mutations and methylation state in human leukemias

Oncogene, 1989-08, Vol.4 (8), p.1029-1036

1989

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Graft-versus-host disease following interferon therapy for relapsed chronic myeloid leukaemia post-allogeneic bone marrow transplantation

Bone marrow transplantation (Basingstoke), 1994-10, Vol.14 (4), p.641-644

1994

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Isolated expression of the Muir-Torre phenotype in a member of a family with hereditary non-polyposis colorectal cancer

Histopathology, 1995-12, Vol.27 (6), p.573-575

1995

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Two missense mutations identified in venous thrombosis patients impair the inhibitory function of the protein Z dependent protease inhibitor

Thrombosis and haemostasis, 2012-05, Vol.107 (5), p.854-863

2012

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Analysis of Ha-ras 1 allele frequencies in hereditary non-polyposis colorectal cancer

Gut, 1995-03, Vol.36 (3), p.382-384

1995

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A polymerase chain reaction‐based method for the detection of trisomy 12 in B chronic lymphocytic leukaemia

British journal of haematology, 1993-09, Vol.85 (1), p.179-181

1993

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Osteoarthritis of the hip: the patient behind the disease

Annals of the rheumatic diseases, 1982-04, Vol.41 (2), p.118-125

1982

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Successful treatment of veno-occlusive disease with recombinant tissue plasminogen activator in a patient requiring peritoneal dialysis

Bone marrow transplantation (Basingstoke), 1994-10, Vol.14 (4), p.635-636

1994

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Variable Philadelphia breakpoints and potential lineage restriction of bcr rearrangement in acute lymphoblastic leukemia

Blood, 1988-08, Vol.72 (2), p.784-791

1988

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Possible misdiagnosis using the Xba I polymorphism for prenatal diagnosis of haemophilia A

British journal of haematology, 1994-11, Vol.88 (3), p.613-614

1994

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Haemophilia B Leyden arising de novo by point mutation in the putative factor IX promoter region

British journal of haematology, 1991-02, Vol.77 (2), p.191-194

1991

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A comparison of the effects of oral prednisone and inhaled beclomethasone dipropionate on circulating leukocytes

Australian and New Zealand Journal of Medicine, 1996-12, Vol.26 (6), p.800-805

1996

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INDEPENDENT CLONAL ORIGIN OF COEXISTING CHRONIC LYMPHOCYTIC LEUKAEMIA AND MULTIPLE MYELOMA

British journal of haematology, 1988-09, Vol.70 (1), p.126-127

1988

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Factor VIII gene inversions in severe hemophilia a patients

Pathology, 1995, Vol.27 (1), p.83-85

1995

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Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer

Australian and New Zealand Journal of Medicine, 1994-12, Vol.24 (6), p.682-686

1994

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Gene probe analysis demonstrates independent clonal evolution of co‐existent chronic myeloid and chronic lymphocytic leukaemia

European journal of haematology, 1988-02, Vol.40 (2), p.181-184

1988

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Interim results for the phase II study of panobinostat (LBH589) in patients (Pts) with relapsed/refractory Hodgkin's lymphoma (HL) after autologous hematopoietic stem cell transplant (AHSCT)

Journal of clinical oncology, 2010-05, Vol.28 (15_suppl), p.8007-8007

2010

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The t(9;22) translocation in Philadelphia-positive essential thrombocythaemia does not involve the T lymphocyte lineage

Acta haematologica, 1990, Vol.83 (4), p.203-205

1990

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FAMILIAL GIANT HYPERPLASTIC POLYPOSIS PREDISPOSING TO COLORECTAL CANCER: A NEW HEREDITARY BOWEL CANCER SYNDROME

P687: A PHASE 1 STUDY WITH THE NOVEL B‐CELL LYMPHOMA 2 (BCL2) INHIBITOR BGB‐11417 AS MONOTHERAPY OR IN COMBINATION WITH ZANUBRUTINIB (ZANU) IN PATIENTS (PTS) WITH B‐CELL MALIGNANCIES: PRELIMINARY DATA

Diagnostic use of microsatellite instability in hereditary non-polyposis colorectal cancer

Factor IX polypyrimidine tract mutation analysis using mRNA from peripheral blood leukocytes

The endothelial protein C receptor (EPCR) 23bp insert in patients with myocardial infarction

Prevalence of factor v leiden and prothrombin variant g20210a in patients age <50 years with no significant stenoses at angiography three to four weeks after myocardial infarction

Colorectal neoplasms detected colonoscopically in at-risk members of colorectal cancer families stratified by the demonstration of DNA microsatellite instability

Analysis of ras gene mutations and methylation state in human leukemias

Graft-versus-host disease following interferon therapy for relapsed chronic myeloid leukaemia post-allogeneic bone marrow transplantation

Isolated expression of the Muir-Torre phenotype in a member of a family with hereditary non-polyposis colorectal cancer

Two missense mutations identified in venous thrombosis patients impair the inhibitory function of the protein Z dependent protease inhibitor

Analysis of Ha-ras 1 allele frequencies in hereditary non-polyposis colorectal cancer

A polymerase chain reaction‐based method for the detection of trisomy 12 in B chronic lymphocytic leukaemia

Osteoarthritis of the hip: the patient behind the disease

Successful treatment of veno-occlusive disease with recombinant tissue plasminogen activator in a patient requiring peritoneal dialysis

Variable Philadelphia breakpoints and potential lineage restriction of bcr rearrangement in acute lymphoblastic leukemia

Possible misdiagnosis using the Xba I polymorphism for prenatal diagnosis of haemophilia A

Haemophilia B Leyden arising de novo by point mutation in the putative factor IX promoter region

A comparison of the effects of oral prednisone and inhaled beclomethasone dipropionate on circulating leukocytes

INDEPENDENT CLONAL ORIGIN OF COEXISTING CHRONIC LYMPHOCYTIC LEUKAEMIA AND MULTIPLE MYELOMA

Factor VIII gene inversions in severe hemophilia a patients

Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer

Gene probe analysis demonstrates independent clonal evolution of co‐existent chronic myeloid and chronic lymphocytic leukaemia

Interim results for the phase II study of panobinostat (LBH589) in patients (Pts) with relapsed/refractory Hodgkin's lymphoma (HL) after autologous hematopoietic stem cell transplant (AHSCT)

The t(9;22) translocation in Philadelphia-positive essential thrombocythaemia does not involve the T lymphocyte lineage

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