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Impaired platelet function in Hermansky-Pudlak syndrome associated with novel mutations in HPS3, HPS6 and HPS8 genes
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722PDF: 156 -
A case of acquired factor XIII deficiency secondary to plasmablastic lymphoma
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676PDF: 348 -
Recent advances in classic heparin-induced thrombocytopenia (HIT), autoimmune HIT, spontaneous HIT, and vaccine-induced immune thrombotic thrombocytopenia
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1876PDF: 505 -
Allopurinol-induced acquired von Willebrand syndrome
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1578PDF: 185 -
The intriguing association between cancer and congenital bleeding disorders
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177PDF: 59 -
Safety of COVID-19 mRNA vaccination in patients with history of acquired hemophilia A: a case series
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2385PDF: 223 -
ReDIP, the Italian network for the diagnosis of congenital platelet function disorders
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350PDF: 112 -
Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond
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1106PDF: 267 -
Comments on “Safe and effective anticoagulation use: case studies in anticoagulation stewardship”
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226PDF: 79 -
The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art
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857PDF: 197SUPPLEMENTARY MATERIAL: 91 -
Gene transfer in hemophilia B: a big step forward
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866PDF: 260 -
Thrombosis and hemostasis at the University of Padua: a reappraisal on the occasion of its 800th year of history
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1981PDF: 219
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