Literature DB >> 4995085

Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.

A Girolami, M Lazzarin, R Scarpa, A Brunetti.   

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Year:  1971        PMID： 4995085

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  8 in total

1.  Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease.

Authors:  A Girolami; A Carli; R Falomo; L De Marco
Journal:  Blut       Date:  1973-09

2.  Factor X level in coumarin treated patients and in factor X deficiency as assayed with different techniques.

Authors:  A Girolami; A Brunetti; G Bareggi
Journal:  Blut       Date:  1972-08

3.  Molecular deficiencies of human blood coagulation.

Authors:  E A Beck
Journal:  Experientia       Date:  1972-01-15

4.  A family with heterozygous factor X Friuli defect outside Friuli.

Authors:  A Girolami; M Lazzarin; M Procidano; G Luzzatto
Journal:  Blut       Date:  1983-03

5.  A new family with classical factor X deficiency as demonstrated by electroimmunoassay.

Authors:  A Girolami; G Luzzatto; N Scattolo; F A Zanolli
Journal:  Blut       Date:  1983-07

6.  The K-test (trypsin clotting time) in coumarin treated patients and in congenital deficiencies and abnormalities of the prothrombin complex.

Authors:  A Girolami; A Brunetti; G Patrassi; F Cafiero
Journal:  Blut       Date:  1975-11

7.  Factor X Friuli: An immunological study in plasma and in serum using several methods.

Authors:  A Girolami; G Bareggi; N Borsato
Journal:  Blut       Date:  1975-03

8.  Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease.

Authors:  A Girolami; F Fabris; G Cappellato; L Sainati; G Boeri
Journal:  Blut       Date:  1983-08
  8 in total

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