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Journal of Hypertension|August 1, 1986
A role for steroid hormones in the variability of blood pressure determinationG de Simone, L Di Lorenzo, A P Tommaselli, et al.
Journal of Thrombosis and Haemostasis : JTH|December 30, 2015
Biosimilars of low-molecular-weight heparin products: fostering competition or reducing 'biodiversity'?J Harenberg, C Cimminiello, G Agnelli, et al.
The American Journal of Medicine|November 1, 1985
Platelet dysfunction in uremia. Multifaceted defect partially corrected by dialysisG Di Minno, J Martinez, M L McKean, et al.
Electrophoresis|April 27, 1999
Determining sulfur-containing amino acids by capillary electrophoresis: a fast novel method for total homocyst(e)ine human plasmaG Vecchione, M Margaglione, E Grandone, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 4, 1998
The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery diseaseM Margaglione, G Cappucci, D Colaizzo, et al.
Journal of Internal Medicine|September 25, 2002
Long-lasting intestinal bleeding in an old patient with multiple mucosal vascular abnormalities and Glanzmann's thrombasthenia: 3-year pharmacological managementA Coppola, V De Stefano, A Tufano, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 8, 2008
Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern ItalyV Sanna, F Zarrilli, P Nardiello, et al.
La Ricerca in Clinica E in Laboratorio|April 1, 1987
Morphological and functional abnormalities in platelets exposed in vitro to ioglicinic acid, a new ionic contrast mediumM De Caterina, A Ruocco, M Violini, et al.
European Journal of Internal Medicine|November 17, 2001
Severe pancytopenia and intrahepatic cholestasis in a patient with a history of Hodgkin's disease. Responsiveness to high-dose pulse steroid therapy and diagnosis of a late relapseA Coppola, A Camera, A Pagano, et al.
Thrombosis and Haemostasis|January 5, 2002
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni RotondoM Margaglione, G Vecchione, R Santacroce, et al.
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