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Journal Articles

Leukocytosis as an Independent Risk Factor for Thrombosis in Polycythemia Vera.

Raffaele Landolfi, MD, Leonardo Di Gennaro, MD, Tiziano Barbui, MD, Valerio De Stefano, MD, Rosamaria Marfisi, MSc, Gianni Tognoni, MD, Francesco Equitani, MD, Guido Finazzi, MD, Roberto Marchioli, MD

Blood (2006) 108 (11): 115.

https://doi.org/10.1182/blood.V108.11.115.115

Published: 2006

Journal Articles

Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera

Raffaele Landolfi, Leonardo Di Gennaro, Tiziano Barbui, Valerio De Stefano, Guido Finazzi, RosaMaria Marfisi, Gianni Tognoni, Roberto Marchioli, for the European Collaboration on Low-Dose Aspirin in Polycythemia Vera (ECLAP)

Blood (2006) 109 (6): 2446–2452.

https://doi.org/10.1182/blood-2006-08-042515

Published: 2006

Includes: Supplemental data

Journal Articles

Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study

Guido Finazzi, Vanesa Caruso, Roberto Marchioli, Giovanni Capnist, Teodoro Chisesi, Carlo Finelli, Luigi Gugliotta, Raffaele Landolfi, Jack Kutti, Heinz Gisslinger, Raphael Marilus, Carlo Patrono, Enrico Maria Pogliani, Maria Luigia Randi, Ana Villegas, Gianni Tognoni, Tiziano Barbui, for the ECLAP Investigators

Blood (2005) 105 (7): 2664–2670.

https://doi.org/10.1182/blood-2004-09-3426

Published: 2005

Journal Articles

Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype

Sepideh Akhavan, Raimondo De Cristofaro, Flora Peyvandi, Silvia Lavoretano, Raffaele Landolfi, Pier M. Mannucci

Blood (2002) 100 (4): 1347–1353.

https://doi.org/10.1182/blood-2002-01-0243

Published: 2002

Journal Articles

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Amos Toren, Galit Rozenfeld-Granot, Bianca Rocca, Charles J. Epstein, Ninette Amariglio, Ferdinando Laghi, Raffaele Landolfi, Frida Brok-Simoni, Lena E. Carlsson, Gideon Rechavi, Andreas Greinacher

Blood (2000) 96 (10): 3447–3451.

https://doi.org/10.1182/blood.V96.10.3447

Published: 2000

Journal Articles

Chromosome Band 1p36 Contains a Putative Tumor Suppressor Gene Important in the Evolution of Chronic Myelocytic Leukemia

Naoki Mori, Roberta Morosetti, Susanne Spira, Stephen Lee, Dina Ben-Yehuda, Gary Schiller, Raffaele Landolfi, Hideaki Mizoguchi, H. Phillip Koeffler

Blood (1998) 92 (9): 3405–3409.

https://doi.org/10.1182/blood.V92.9.3405

Published: 1998

Journal Articles

Allelotype Analysis in the Evolution of Chronic Myelocytic Leukemia

Naoki Mori, Roberta Morosetti, Stephen Lee, Susanne Spira, Dina Ben-Yehuda, Gary Schiller, Raffaele Landolfi, Hideaki Mizoguchi, H. Phillip Koeffler

Blood (1997) 90 (5): 2010–2014.

https://doi.org/10.1182/blood.V90.5.2010

Published: 1997

NARROW

Leukocytosis as an Independent Risk Factor for Thrombosis in Polycythemia Vera.

Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera

Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study

Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Chromosome Band 1p36 Contains a Putative Tumor Suppressor Gene Important in the Evolution of Chronic Myelocytic Leukemia

Allelotype Analysis in the Evolution of Chronic Myelocytic Leukemia

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ASH Publications

American Society of Hematology

Leukocytosis as an Independent Risk Factor for Thrombosis in Polycythemia Vera.

Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera

Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study

Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Chromosome Band 1p36 Contains a Putative Tumor Suppressor Gene Important in the Evolution of Chronic Myelocytic Leukemia

Allelotype Analysis in the Evolution of Chronic Myelocytic Leukemia

Email alerts

ASH Publications

American Society of Hematology

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