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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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711PDF: 152 -
A case of acquired factor XIII deficiency secondary to plasmablastic lymphoma
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667PDF: 344 -
Recent advances in classic heparin-induced thrombocytopenia (HIT), autoimmune HIT, spontaneous HIT, and vaccine-induced immune thrombotic thrombocytopenia
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1853PDF: 495 -
Allopurinol-induced acquired von Willebrand syndrome
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1569PDF: 182 -
The intriguing association between cancer and congenital bleeding disorders
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170PDF: 57 -
Safety of COVID-19 mRNA vaccination in patients with history of acquired hemophilia A: a case series
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2380PDF: 222 -
ReDIP, the Italian network for the diagnosis of congenital platelet function disorders
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341PDF: 110 -
Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond
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1095PDF: 263 -
Gene transfer in hemophilia B: a big step forward
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855PDF: 254 -
Thrombosis and hemostasis at the University of Padua: a reappraisal on the occasion of its 800th year of history
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1970PDF: 217 -
The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art
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832PDF: 189SUPPLEMENTARY MATERIAL: 89