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Haematologia|January 1, 1994
Symptomatic versus asymptomatic patients in congenital hypoplasminogenemia: a statistical analysisA Girolami, M T Sartori, G Saggiorato, et al.
Meat Science|November 9, 2011
Chemical composition of pig meat from the genetic type 'Casertana' and its crossbreedsA Zullo, C M A Barone, P Colatruglio, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
The report of an Italian family with heterozygous protein C deficiencyA Girolami, M G Cappellato, A R Lazzaro, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 28, 2007
Heparin induced thrombocytopenia: pathogenetic, clinical, diagnostic and therapeutic aspectsR Castelli, E Cassinerio, M D Cappellini, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 1, 2001
Treatment of heterozygous familial hypercholesterolemia: atorvastatin vs simvastatinM Bo, M T Nicolello, U Fiandra, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 27, 2003
Psychological aspects and coping in haemophilic patients: a case-control studyM Canclini, N Saviolo-Negrin, E Zanon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 24, 1999
Psychological aspects and coping of parents with a haemophilic child: a quantitative approachN Saviolo-Negrin, F Cristante, E Zanon, et al.
British Journal of Haematology|March 22, 2001
Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co-factor activity?A Casonato, E Pontara, A Bertomoro, et al.
Haematologia|January 1, 1993
Combined haemophilia A and type I von Willebrand's disease: a family study including an evaluation of the effects of DDAVP infusionA Casonato, E Pontara, M Boscaro, et al.
Biochimica Et Biophysica Acta|March 20, 1993
The dysfunction of coagulation factor VIIPadua results from substitution of arginine-304 by glutamineH L James, A Girolami, J G Hubbard, et al.
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