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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2018-11, Vol.16 (11), p.2341-2346

2018

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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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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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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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Inherited thrombocytopenias: the evolving spectrum

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

2012

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Platelet count and aging

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

2014

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Inherited thrombocytopenias in the era of personalized medicine

Haematologica (Roma), 2015-02, Vol.100 (2), p.145-148

2015

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Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

Nature genetics, 2000-09, Vol.26 (1), p.103-105

Syndrome Consortium, The May-Hegglin/Fechtner

2000

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[beta]-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

2015

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Laboratory monitoring of P2Y 12 inhibitors: communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2018-11, Vol.16 (11), p.2341

2018

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Role of physical activity and metabolic syndrome in determining the risk of postmenopausal breast cancer: a systematic review

International Journal Of Community Medicine And Public Health, 2021-06, Vol.8 (7), p.3561

2021

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Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

American journal of kidney diseases, 2003-01, Vol.41 (1), p.95-104

2003

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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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Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients

Haematologica (Roma), 2004-10, Vol.89 (10), p.1219

2004

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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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Ristocetin-induced platelet agglutination stimulates GPIIb/IIIa-dependent calcium influx

Thrombosis and haemostasis, 1995-04, Vol.73 (4), p.689-692

1995

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Immunocytochemistry for the heavy chain of the non‐muscle myosin IIA as a diagnostic tool for MYH9‐related disorders

British journal of haematology, 2002-04, Vol.117 (1), p.164-167

2002

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Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb (Bolzano mutation)

Haematologica (Roma), 2012-01, Vol.97 (1), p.82-88

2012

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Platelet aggregation in platelet-rich plasma and whole blood in 120 patients with myeloproliferative disorders

American journal of clinical pathology, 1991, Vol.95 (1), p.82-86

1991

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In vitro and in vivo effects of desmopressin on platelet function

Haematologica (Roma), 1999-10, Vol.84 (10), p.891

1999

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Dominant inheritance of a novel integrin {beta}3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families

Haematologica (Roma), 2009-05, Vol.94 (5), p.663-669

2009

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CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA (CAMT): CLINICAL AND BIOLOGICAL CHARACTERIZATION OF FIVE NEW MUTATIONS

Journal of thrombosis and haemostasis, 2007-07, Vol.5, p.P-M-189-P-M-189

2007

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Cryopreservation of human platelets using dimethyl sulfoxide and glycerol-glucose: effects on "in vitro" platelet function

Haematologica (Roma), 1993-03, Vol.78 (2), p.101

1993

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Maxa, A New Low-Frequency Platelet-Specific Antigen Localized on Glycoprotein IIb, Is Associated With Neonatal Alloimmune Thrombocytopenia

Blood, 1995-08, Vol.86 (3), p.1019-1026

1995

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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH

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

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

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

Inherited thrombocytopenias: the evolving spectrum

Platelet count and aging

Inherited thrombocytopenias in the era of personalized medicine

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

[beta]-1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

Laboratory monitoring of P2Y 12 inhibitors: communication from the SSC of the ISTH

Role of physical activity and metabolic syndrome in determining the risk of postmenopausal breast cancer: a systematic review

Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

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

Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients

Thrombopoietin levels in patients with primary and reactive thrombocytosis

Ristocetin-induced platelet agglutination stimulates GPIIb/IIIa-dependent calcium influx

Immunocytochemistry for the heavy chain of the non‐muscle myosin IIA as a diagnostic tool for MYH9‐related disorders

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb (Bolzano mutation)

Platelet aggregation in platelet-rich plasma and whole blood in 120 patients with myeloproliferative disorders

In vitro and in vivo effects of desmopressin on platelet function

Dominant inheritance of a novel integrin {beta}3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families

CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA (CAMT): CLINICAL AND BIOLOGICAL CHARACTERIZATION OF FIVE NEW MUTATIONS

Cryopreservation of human platelets using dimethyl sulfoxide and glycerol-glucose: effects on "in vitro" platelet function

Maxa, A New Low-Frequency Platelet-Specific Antigen Localized on Glycoprotein IIb, Is Associated With Neonatal Alloimmune Thrombocytopenia

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