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Thrombosis and Haemostasis|February 1, 1996
Characterization of recombinant human coagulation factor XFriuliD J Kim, A Girolami, H L JamesBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1994
Prothrombin Padua I: incomplete activation due to an amino acid substitution at a factor Xa cleavage siteH L James, D J Kim, D Q Zheng, et al.Blood|January 15, 1991
Molecular defect in coagulation factor XFriuli results from a substitution of serine for proline at position 343H L James, A Girolami, D S FairBiochimica 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.Human Genetics|February 1, 1995
Factor XKetchikan: a variant molecule in which Gly replaces a Gla residue at position 14 in the light chainD J Kim, A R Thompson, H L JamesFolia Haematologica (Leipzig, Germany : 1928)|January 1, 1980
The congenital factor VII abnormalities (dysproconvertinemias). The genetic plot thickensA GirolamiArchivos Del Instituto De Cardiologia De Mexico|July 10, 1998
Low molecular weight heparins in clinical practice: unsolved or partially solved problemsA GirolamiFolia Haematologica (Leipzig, Germany : 1928)|January 1, 1987
A tentative classification of AT III congenital abnormalitiesA GirolamiClinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|November 8, 2001
Idiopathic deep vein thrombosis and subsequent cancer: suggestions for a patient-oriented and practical approachA GirolamiFolia Haematologica (Leipzig, Germany : 1928)|January 1, 1978
Evidence against the presence of "inhibitors" in coumarin treated patientsA GirolamiPageof 104