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Thrombopoietin receptor agonists in hereditary thrombocytopenias

Journal of thrombosis and haemostasis, 2018-09, Vol.16 (9), p.1700-1710

2018

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Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

Journal of thrombosis and haemostasis, 2017-07, Vol.15 (7), p.1511-1521

2017

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Inherited thrombocytopenias frequently diagnosed in adults

Journal of thrombosis and haemostasis, 2013-06, Vol.11 (6), p.1006-1019

2013

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Adhesive receptors, extracellular proteins and myosin IIA orchestrate proplatelet formation by human megakaryocytes

Journal of thrombosis and haemostasis, 2008-11, Vol.6 (11), p.1900-1907

2008

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Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.673-681

2017

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Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future

Haematologica (Roma), 2016-01, Vol.101 (1), p.2-4

2016

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Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano

Journal of thrombosis and haemostasis, 2009-03, Vol.7 (3), p.478-484

2009

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Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?

Journal of thrombosis and haemostasis, 2017-11, Vol.15 (11), p.2226-2229

2017

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Altered cytoskeleton organization in platelets from patients with MYH9‐related disease

Journal of thrombosis and haemostasis, 2005-05, Vol.3 (5), p.1026-1035

2005

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Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Haematologica (Roma), 2011-03, Vol.96 (3), p.417-423

2011

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Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

Journal of thrombosis and haemostasis, 2009-12, Vol.7 (12), p.2131-2136

2009

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β‐1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.651-659

2015

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Cord blood in vitro expanded CD41+ cells: identification of novel components of megakaryocytopoiesis

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.848-860

2006

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Inherited thrombocytopenias: the evolving spectrum

Hämostaseologie, 2012, Vol.32 (4), p.259-270

2012

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Management of bleeding and of invasive procedures in patients with platelet disorders and/or thrombocytopenia: Guidelines of the Italian Society for Haemostasis and Thrombosis (SISET)

Thrombosis research, 2009-11, Vol.124 (5), p.e13-e18

2009

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Thrombopoietin levels in patients with primary and reactive thrombocytosis

British journal of haematology, 1997-11, Vol.99 (2), p.281-284

1997

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Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

Leukemia, 2001-12, Vol.15 (12), p.1885-1891

2001

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Thrombocytopenia, Giant Platelets, and Leukocyte Inclusion Bodies (May-Hegglin Anomaly): Clinical and Laboratory Findings

The American journal of medicine, 1998-04, Vol.104 (4), p.355-360

1998

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Revealing eltrombopag's promotion of human megakaryopoiesis through AKT/ERK-dependent pathway activation

Haematologica (Roma), 2016-12, Vol.101 (12), p.1479-1488

2016

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International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

Journal of thrombosis and haemostasis, 2012-08, Vol.10 (8), p.1653-1661

2012

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Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

Haematologica (Roma), 2007-09, Vol.92 (9), p.1186-1193

2007

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Platelet count and aging

Haematologica (Roma), 2014-06, Vol.99 (6), p.953-955

2014

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Circulating thrombopoietin in reactive conditions behaves like an acute phase reactant

Clinical and laboratory haematology, 1999-08, Vol.21 (4), p.271-275

1999

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Relationship between size and thiazole orange fluorescence of platelets in patients undergoing high‐dose chemotherapy

British journal of haematology, 1999-07, Vol.106 (1), p.202-207

1999

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The Gene for May-Hegglin Anomaly Localizes to a <1-Mb Region on Chromosome 22q12.3-13.1

American journal of human genetics, 2000-04, Vol.66 (4), p.1449-1454

2000

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Thrombopoietin receptor agonists in hereditary thrombocytopenias

Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

Inherited thrombocytopenias frequently diagnosed in adults

Adhesive receptors, extracellular proteins and myosin IIA orchestrate proplatelet formation by human megakaryocytes

Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias

Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future

Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano

Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?

Altered cytoskeleton organization in platelets from patients with MYH9‐related disease

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

β‐1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

Cord blood in vitro expanded CD41+ cells: identification of novel components of megakaryocytopoiesis

Inherited thrombocytopenias: the evolving spectrum

Management of bleeding and of invasive procedures in patients with platelet disorders and/or thrombocytopenia: Guidelines of the Italian Society for Haemostasis and Thrombosis (SISET)

Thrombopoietin levels in patients with primary and reactive thrombocytosis

Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

Thrombocytopenia, Giant Platelets, and Leukocyte Inclusion Bodies (May-Hegglin Anomaly): Clinical and Laboratory Findings

Revealing eltrombopag's promotion of human megakaryopoiesis through AKT/ERK-dependent pathway activation

International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

Platelet count and aging

Circulating thrombopoietin in reactive conditions behaves like an acute phase reactant

Relationship between size and thiazole orange fluorescence of platelets in patients undergoing high‐dose chemotherapy

The Gene for May-Hegglin Anomaly Localizes to a <1-Mb Region on Chromosome 22q12.3-13.1

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