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Articles by Antonio Girolami

A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys)

Girolami, Antonio; Molina, Maria Angelica; Galletti, Maria Laura Lopez; More

Blood Coagulation & Fibrinolysis. 27(6):732-736, September 2016.

Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and –13C>T promoter region in three compound heterozygotes

Lombardi, Anna Maria; Bortoletto, Elisabetta; Scarparo, Pamela; More

Blood Coagulation & Fibrinolysis. 19(7):639-643, October 2008.