A family with heterozygous factor X friuli defect outside friuli

[1]  A. Girolami,et al.  Factor X Friuli coagulation disorder , 1973, Blut.

[2]  R. Bertina,et al.  A Variant of Factor X That Is Defective Only In Extrinsic Coagulation , 1981, Thrombosis and Haemostasis.

[3]  A. Girolami,et al.  Factor X assays using chromogenic substrate S-2222. , 1980, American journal of clinical pathology.

[4]  K. Lechner,et al.  Factor X Vorarlberg, a New Variant of Hereditary Factor X DeficiencyX , 1979, Thrombosis and Haemostasis.

[5]  A. Girolami,et al.  Factor X Friuli coagulation disorder. Report of a newly recognized patient and some considerations on the frequency of the disease in the Friuli area. , 1976, Acta haematologica.

[6]  A. Girolami,et al.  Classical Factor X Deficiency , 1975 .

[7]  A. Girolami,et al.  Classical factor X deficiency. Report of a further case. , 1975, Acta haematologica.

[8]  A. Girolami,et al.  Abnormal factor X (factor X Friuli) coagulation disorder. The heterozygote population. A study of 57 subjects. , 1974, Acta haematologica.

[9]  A. Girolami,et al.  Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease. , 1973, Blut.

[10]  A. Girolami,et al.  Abnormal factor X(factor X Friuli) coagulation disorder. , 1973, Acta haematologica.

[11]  A. Girolami,et al.  Crossover electrophoresis (electrosyneresis) visualization of the abnormal factor X (factor X Friuli). , 1972, The Journal of laboratory and clinical medicine.

[12]  A. Girolami,et al.  Different Cross-Over Electrophoretic Mobility of Factor Friuli X and Coumarin-induced Abnormal Factor X , 1972 .

[13]  R. Scarpa,et al.  Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family. , 1971, Blood.

[14]  A. Girolami,et al.  Prothrombin Level and Activity in the Abnormal Factor X (Factor X Friuli) Hemorrhagic Disorder , 1971, Thrombosis and Haemostasis.

[15]  R. Scarpa,et al.  Congenital haemorrhagic condition similar but not identical to factor X deficiency. A haemorrhagic state due to an abnormal factor X? , 2009, Scandinavian journal of haematology.

[16]  A. Girolami,et al.  Severe Congenital Factor X Deficiency in 5-Month-Old Child , 1970, Thrombosis and Haemostasis.

[17]  R. Scarpa,et al.  A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred , 1970, British journal of haematology.

[18]  A. Girolami,et al.  [A new congenital hemorrhagic coagulation disorder probably due to the presence of an abnormal factor X. Preliminary study]. , 1969, Minerva medica.

[19]  C. Hougie,et al.  Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state. , 1957, The Journal of clinical investigation.

[20]  C. Hougie,et al.  Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency. , 1957, The Journal of clinical investigation.

[21]  F. Bachmann,et al.  Über einen neuartigen kongenitalen Gerinnungsdefekt (Mangel an Stuart-Faktor) , 1957, Thrombosis and Haemostasis.

[22]  K. Denson,et al.  A ‘New’ Coagulation Defect , 1956, British journal of haematology.