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Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

Haematologica (Roma), 2019-10, Vol.104 (10), p.2084-2090

2019

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Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3

Platelets (Edinburgh), 2020-10, Vol.31 (7), p.1-963

2020

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Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignancies

Platelets (Edinburgh), 2019-11, Vol.30 (8), p.1053-1056

2019

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P2Y12 receptor gene mutations associated with bleeding

Platelets (Edinburgh), 2017-06, Vol.28 (4), p.421-423

2017

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Clearance of circulating activated platelets in polycythemia vera and essential thrombocythemia

Blood, 2011-09, Vol.118 (12), p.3359-3366

2011

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Patients with Essential Thrombocythemia may be Poor Responders to Enteric-Coated Aspirin, but not to Plain Aspirin

Thrombosis and haemostasis, 2020-10, Vol.120 (10), p.1442-1453

2020

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Comprehensive investigation of platelet function in patients with cirrhosis

Thrombosis research, 2024-05, Vol.237, p.64-70

2024

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Usefulness of the INNOVANCE® PFA P2Y test cartridge for the detection of patients with congenital defects of the platelet P2Y12 receptor for adenosine diphosphate

Thrombosis research, 2014-02, Vol.133 (2), p.254-256

2014

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Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency

Thrombosis and haemostasis, 2014-12, Vol.112 (6), p.1182-1189

2014

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Instability of cytosolic phospholipase A2α variant upon cellular expression as a basis for its clinical presentation

Thrombosis and haemostasis, 2015, Vol.114 (1), p.208-210

2015

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Zonisamide in the management of epilepsy in the elderly

Clinical interventions in aging, 2015-01, Vol.10, p.931-937

2015

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EV-077 in vitro inhibits platelet aggregation in type-2 diabetics on aspirin

Thrombosis research, 2012-11, Vol.130 (5), p.746-752

2012

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P2Y 12 receptor gene mutations associated with bleeding

Platelets (Edinburgh), 2017-05, Vol.28 (4), p.421-423

2017

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Studies of the interaction of ticagrelor with the P2Y13 receptor and with P2Y13-dependent pro-platelet formation by human megakaryocytes

Thrombosis and haemostasis, 2016-11, Vol.116 (12), p.1079-1088

2016

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Inherited dysfunctional platelet P2Y12 receptor mutations associated with bleeding disorders

Hämostaseologie, 2016, Vol.36 (4), p.279-283

2016

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A simple strategy for the synthesis of the glycosylated collagen biomarkers α- d-glucopyranosyl-(1→2)-β- d-galactopyranosyl- O-pyridinoline (Glc-Gal-PYD), α- d-glucopyranosyl-(1→2)-β- d-galactopyranosyl-5- O-hydroxylysine (Glc-Gal-Hyl) and of their unnatural epimers Glc-Gal- epiPYD and Glc-Gal- epiHyl

Tetrahedron: asymmetry, 2007-11, Vol.18 (22), p.2689-2694

2007

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Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignancies

Platelets, 2019, Vol.30 (8), p.1053-1056

2019

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Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3

Platelets, 2020, Vol.31 (7), p.960-963

2020

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Studies of the interaction of ticagrelor with the P2Y 13 receptor and with P2Y 13 -dependent pro-platelet formation by human megakaryocytes

Thrombosis and haemostasis, 2016-11, Vol.116 (6), p.1079

2016

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Qualitative Platelet Disorders

Practical Hemostasis and Thrombosis, 2017, p.160-171

2017

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Inherited dysfunctional platelet P2Y 12 receptor mutations associated with bleeding disorders

Hamostaseologie, 2016-11, Vol.36 (4), p.279

2016

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In-vitro and in-vivo metabolism of different aspirin formulations studied by a validated liquid chromatography tandem mass spectrometry method

Scientific reports, 2021-05, Vol.11 (1), p.10370-10, Article 10370

2021

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A case of acquired transient bleeding diathesis associated with acquired platelet storage pool deficiency and defective thromboxane A2 production

Platelets (Edinburgh), 2024-12, Vol.35 (1), p.2358241

2024

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Inhibition of the platelet P2Y12 receptor for adenosine diphosphate does not impair the capacity of platelet to synthesize thromboxane A2

European heart journal, 2016-11, Vol.37 (44), p.3347-3356

2016

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Blood Cell-Bound C4d as a Marker of Complement Activation in Patients With the Antiphospholipid Syndrome

Frontiers in immunology, 2019-04, Vol.10, p.773-773

2019

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Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3

Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignancies

P2Y12 receptor gene mutations associated with bleeding

Clearance of circulating activated platelets in polycythemia vera and essential thrombocythemia

Patients with Essential Thrombocythemia may be Poor Responders to Enteric-Coated Aspirin, but not to Plain Aspirin

Comprehensive investigation of platelet function in patients with cirrhosis

Usefulness of the INNOVANCE® PFA P2Y test cartridge for the detection of patients with congenital defects of the platelet P2Y12 receptor for adenosine diphosphate

Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency

Instability of cytosolic phospholipase A2α variant upon cellular expression as a basis for its clinical presentation

Zonisamide in the management of epilepsy in the elderly

EV-077 in vitro inhibits platelet aggregation in type-2 diabetics on aspirin

P2Y 12 receptor gene mutations associated with bleeding

Studies of the interaction of ticagrelor with the P2Y13 receptor and with P2Y13-dependent pro-platelet formation by human megakaryocytes

Inherited dysfunctional platelet P2Y12 receptor mutations associated with bleeding disorders

Acquired platelet dysfunction and overproduction of platelet cyclic AMP in two patients with myeloid malignancies

Novel variant in HPS3 gene in a patient with Hermansky Pudlak syndrome (HPS) type 3

Studies of the interaction of ticagrelor with the P2Y 13 receptor and with P2Y 13 -dependent pro-platelet formation by human megakaryocytes

Qualitative Platelet Disorders

Inherited dysfunctional platelet P2Y 12 receptor mutations associated with bleeding disorders

In-vitro and in-vivo metabolism of different aspirin formulations studied by a validated liquid chromatography tandem mass spectrometry method

A case of acquired transient bleeding diathesis associated with acquired platelet storage pool deficiency and defective thromboxane A2 production

Inhibition of the platelet P2Y12 receptor for adenosine diphosphate does not impair the capacity of platelet to synthesize thromboxane A2

Blood Cell-Bound C4d as a Marker of Complement Activation in Patients With the Antiphospholipid Syndrome

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