Factor X Friuli

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

[2]  A. Girolami,et al.  Factor X survival and therapeutic factor X levels in the abnormal factor X (factor X FRIULI) COAGULATION DISORDER. , 1974, Acta haematologica.

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

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

[5]  A. Girolami,et al.  The Effect of Several Tissue Thromboplastins on the Activation of the Abnormal Factor X (Factor X Friuli) , 1972, Thrombosis and Haemostasis.

[6]  H. Hemker,et al.  Lack of PIVKA effect in the abnormal factor X (factor X Friuli) coagulation disorder. , 1972, Haemostasis.

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

[8]  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.

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

[10]  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.

[11]  R. Scarpa,et al.  Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family. , 1970, Haematologica Latina.

[12]  P. Mannucci,et al.  The Factor‐X Defect: Recognition of Abnormal Forms of Factor X , 1970, British journal of haematology.

[13]  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.

[14]  H. Roberts,et al.  THE INHERITANCE OF STUART DISEASE: INVESTIGATION OF A FAMILY WITH FACTOR X DEFICIENCY' , 1965, The American journal of the medical sciences.

[15]  J. Roos,et al.  GENETIC INVESTIGATION OF THE STUART COAGULATION DEFECT , 1959 .

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

[17]  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.

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