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Haematologica|December 23, 2003
An antifibrinolytic effect associated with an anti-factor V antibody in a patient with severe thrombophiliaMario Colucci, Paolo Simioni, Donatella Piro, et al.
Haematologica|December 23, 2003
Uncontrolled-rate freezing of peripheral blood progenitor cells allows successful engraftment by sparing primitive and committed hematopoietic progenitorsCamillo Almici, Piero Ferremi, Arnalda Lanfranchi, et al.
Haematologica|December 23, 2003
Dendritic cell viability is decreased after phagocytosis of apoptotic tumor cells induced by staurosporine or vaccinia virus infectionMassimo Di Nicola, Sara Napoli, Andrea Anichini, et al.
Haematologica|December 23, 2003
Utility of percutaneous lung biopsy for diagnosing filamentous fungal infections in hematologic malignanciesAnnamaria Nosari, Michela Anghilieri, Gianpaolo Carrafiello, et al.
Haematologica|July 1, 1991
Myelopathies during the course of multiple myelomaT Economopoulos, V Pappa, A Panani, et al.
Haematologica|July 1, 1991
Parenchymal brain leukemia. Case report: problems related to the diagnosis and treatmentA Corbetta, M Jankovic, V Conter, et al.
Haematologica|July 1, 1991
A rosetting test with papain-treated erythrocytes (RBC) for the detection of a minor erythrocyte population (chimerism) with different antigenic expressivityE Franchini, T Lanza
Haematologica|September 26, 2008
Anemia of chronic disease and defective erythropoietin production in patients with celiac diseaseGaetano Bergamaschi, Konstantinos Markopoulos, Riccardo Albertini, et al.
Haematologica|September 26, 2008
The relevance of preferentially expressed antigen of melanoma (PRAME) as a marker of disease activity and prognosis in acute promyelocytic leukemiaCarlos Santamaría, María Carmen Chillón, Ramón García-Sanz, et al.
Haematologica|September 26, 2008
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variantSilvia Vettore, Raffaella Scandellari, Stefano Moro, et al.
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