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Journal Articles

Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma

P Simioni, M Kalafatis, DS Millar, SC Henderson, S Luni, DN Cooper, A Girolami
Journal: Blood
Blood (1996) 88 (6): 2101–2108.
https://doi.org/10.1182/blood.V88.6.2101.bloodjournal8862101
Published: 1996
Journal Articles

Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain

T Izumi, T Hashiguchi, G Castaman, A Tosetto, F Rodeghiero, A Girolami, A Ichinose
Journal: Blood
Blood (1996) 87 (7): 2769–2774.
https://doi.org/10.1182/blood.V87.7.2769.bloodjournal8772769
Published: 1996
Journal Articles

Molecular defect in coagulation factor XFriuli results from a substitution of serine for proline at position 343

HL James, A Girolami, DS Fair
Journal: Blood
Blood (1991) 77 (2): 317–323.
https://doi.org/10.1182/blood.V77.2.317.317
Published: 1991
Journal Articles

A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma

A Casonato, L De Marco, M Mazzucato, V De Angelis, D De Roia, F Fabris, ZM Ruggeri, A Girolami
Journal: Blood
Blood (1989) 74 (6): 2028–2033.
https://doi.org/10.1182/blood.V74.6.2028.2028
Published: 1989
Journal Articles

Partial gene deletion in a family with factor X deficiency

F Bernardi, G Marchetti, P Patracchini, S Volinia, D Gemmati, P Simioni, A Girolami
Journal: Blood
Blood (1989) 73 (8): 2123–2127.
https://doi.org/10.1182/blood.V73.8.2123.2123
Published: 1989
Journal Articles

Isolation and characterization of the factor X Friuli variant

DS Fair, DJ Revak, JG Hubbard, A Girolami
Journal: Blood
Blood (1989) 73 (8): 2108–2116.
https://doi.org/10.1182/blood.V73.8.2108.2108
Published: 1989
Journal Articles

Factor VII Padua 2: another factor VII abnormality with defective ox brain thromboplastin activation and a complex hereditary pattern

A Girolami, G Cattarozzi, R Dal Bo Zanon, F Toffanin
Journal: Blood
Blood (1979) 54 (1): 46–53.
https://doi.org/10.1182/blood.V54.1.46.46
Published: 1979
Journal Articles

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency

A Girolami, S Coccheri, G Palareti, M Poggi, A Burul, G Cappellato
Journal: Blood
Blood (1978) 52 (1): 115–125.
https://doi.org/10.1182/blood.V52.1.115.115
Published: 1978
Journal Articles

Factor VII verona coagulation disorder: double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency

A Girolami, G Falezza, G Patrassi, M Stenico, L Vettore
Journal: Blood
Blood (1977) 50 (4): 603–610.
https://doi.org/10.1182/blood.V50.4.603.603
Published: 1977
Journal Articles

Further Studies on the Abnormal Factor X (Factor X Friuli) Coagulation Disorder: A Report of Another Family

A. GIROLAMI, M.D., M. LAZZARIN, M.D., R. SCARPA, M.D., A. BRUNETTI, M.D.
Journal: Blood
Blood (1971) 37 (5): 534–541.
https://doi.org/10.1182/blood.V37.5.534.534
Published: 1971
Journal Articles

The Effect of Ellagic Acid on the Thrombin-Induced Hemorrhagic Syndrome in the Rat

E. E. CLIFFTON, M.D., A. GIROLAMI, M.D., D. AGOSTINO, V.M.D.
Journal: Blood
Blood (1966) 28 (2): 253–257.
https://doi.org/10.1182/blood.V28.2.253.253
Published: 1966