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Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

Leukemia, 2016-04, Vol.30 (4), p.999-1002

2016

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Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets

Journal of thrombosis and haemostasis, 2014-05, Vol.12 (5), p.761-772

2014

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Anagrelide platelet‐lowering effect is due to inhibition of both megakaryocyte maturation and proplatelet formation: insight into potential mechanisms

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.631-642

2015

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Primary myelofibrosis in a patient who developed primary biliary cirrhosis, autoimmune hemolytic anemia and fibrillary glomerulonephritis

Annals of hematology, 2008-12, Vol.87 (12), p.1019-1020

2008

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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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Associated thrombophilic defects in essential thrombocythaemia: their relationship with clinical manifestations

Thrombosis research, 2003, Vol.112 (3), p.131-135

2003

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Production of functional platelet-like particles by the megakaryoblastic DAMI cell line provides a model for platelet biogenesis

Platelets (Edinburgh), 2011-01, Vol.22 (1), p.26-36

2011

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Monocyte IL-2Rα expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms

Cytokine (Philadelphia, Pa.), 2010-07, Vol.51 (1), p.67-72

2010

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Pulmonary Hypertension in Paroxysmal Nocturnal Hemoglobinuria

Chest, 1992-08, Vol.102 (2), p.642-643

1992

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Diverse Mpl expression pattern among pedigrees with inherited thrombocytopenia: potential diagnostic and therapeutic implications

Journal of thrombosis and haemostasis, 2008-12, Vol.6 (12), p.2215-2217

2008

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Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

Thrombosis and haemostasis, 2010-04, Vol.103 (4), p.826-832

2010

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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Haematologica (Roma), 2014-08, Vol.99 (8), p.1387-1394

2014

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A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation

Journal of blood medicine, 2021-01, Vol.12, p.719-732

2021

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and -granule deficiency

Haematologica (Roma), 2013-06, Vol.98 (6), p.868-874

2013

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Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation

Blood, 2005-06, Vol.105 (12), p.4664-4670

2005

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Familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML)

Atlas of genetics and cytogenetics in oncology and haematology, 2011-11 (7)

Heller, PG

2011

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Moyamoya syndrome in an adolescent with essential thrombocythemia: successful intracranial carotid stent placement

Stroke (1970), 2005-08, Vol.36 (8), p.E71-E73

2005

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Familial platelet disorder with predisposition to acute myelogenous leukemia

Atlas of genetics and cytogenetics in oncology and haematology, 2013-02 (2)

2013

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Monocyte IL-2Ralpha expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms

Cytokine (Philadelphia, Pa.), 2010-07, Vol.51 (1), p.67-72

2010

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The clinical course of patients with septic abortion admitted to an intensive care unit

Intensive care medicine, 2004-06, Vol.30 (6), p.1097-1102

2004

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PDGF‐A, PDGF‐B, TGFβ, and bFGF mRNA levels in patients with essential thrombocythemia treated with anagrelide

American journal of hematology, 2005-02, Vol.78 (2), p.155-157

2005

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Catastrophic antiphospholipid syndrome. Communication of 2 forms of presentation

Medicina (Buenos Aires), 1999, Vol.59 (6), p.743

1999

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Primary myelofibrosis in a patient who developed primary biliary cirrhosis, autoimmune hemolytic anemia and fibrillary glomerulonephritis

Annals of hematology, 2008, Vol.87 (12), p.1019-1020

2008

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Alcohol metabolism contributes to brain histone acetylation

Nature (London), 2019-10, Vol.574 (7780), p.717-721

2019

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Follow-up of Blood-Pressure Lowering and Glucose Control in Type 2 Diabetes

The New England journal of medicine, 2014-10, Vol.371 (15), p.1392-1406

2014

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Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets

Anagrelide platelet‐lowering effect is due to inhibition of both megakaryocyte maturation and proplatelet formation: insight into potential mechanisms

Primary myelofibrosis in a patient who developed primary biliary cirrhosis, autoimmune hemolytic anemia and fibrillary glomerulonephritis

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

Associated thrombophilic defects in essential thrombocythaemia: their relationship with clinical manifestations

Production of functional platelet-like particles by the megakaryoblastic DAMI cell line provides a model for platelet biogenesis

Monocyte IL-2Rα expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms

Pulmonary Hypertension in Paroxysmal Nocturnal Hemoglobinuria

Diverse Mpl expression pattern among pedigrees with inherited thrombocytopenia: potential diagnostic and therapeutic implications

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation

Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and -granule deficiency

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation

Familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML)

Moyamoya syndrome in an adolescent with essential thrombocythemia: successful intracranial carotid stent placement

Familial platelet disorder with predisposition to acute myelogenous leukemia

Monocyte IL-2Ralpha expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms

The clinical course of patients with septic abortion admitted to an intensive care unit

PDGF‐A, PDGF‐B, TGFβ, and bFGF mRNA levels in patients with essential thrombocythemia treated with anagrelide

Catastrophic antiphospholipid syndrome. Communication of 2 forms of presentation

Primary myelofibrosis in a patient who developed primary biliary cirrhosis, autoimmune hemolytic anemia and fibrillary glomerulonephritis

Alcohol metabolism contributes to brain histone acetylation

Follow-up of Blood-Pressure Lowering and Glucose Control in Type 2 Diabetes

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