Literature DB >> 4810902

Congenital combined factor V and factor VIII deficiency in a male born from a brother-sister incest.

A Girolami, A Brunetti, L De Marco.   

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Year:  1974        PMID： 4810902     DOI： 10.1007/bf01630657

Source DB:  PubMed          Journal:  Blut        ISSN： 0006-5242


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  15 in total

1.  MEASUREMENT OF PLATELET ADHESIVENESS. A SIMPLE IN VITRO TECHNIQUE DEMONSTRATING AN ABNORMALITY IN VON WILLEBRAND'S DISEASE.

Authors:  E W SALZMAN
Journal:  J Lab Clin Med       Date:  1963-11

2.  A method for the study of antihaemophilic globulin inhibitors with reference to six cases.

Authors:  R BIGGS; E BIDWELL
Journal:  Br J Haematol       Date:  1959-10       Impact factor: 6.998

3.  Combined deficiency of factor V and factor VIII (antihaemophilic globulin). A report of three cases.

Authors:  J H JONES; C R RIZZA; R M HARDISTY; K M DORMANDY; J C MACPHERSON
Journal:  Br J Haematol       Date:  1962-04       Impact factor: 6.998

4.  A report of a case of congenital afibrinogenemia.

Authors:  A Girolami; R Venturelli; G Bareggi
Journal:  Blut       Date:  1972-01

5.  Combined factor-V and factor-VIII deficiency: report of four cases.

Authors:  U Seligsohn; B Ramot
Journal:  Br J Haematol       Date:  1969-05       Impact factor: 6.998

6.  Parahemophilia. A case report.

Authors:  A Girolami; R Venturelli; F Righini; R Scarpa
Journal:  Acta Haematol       Date:  1971       Impact factor: 2.195

7.  A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.

Authors:  A Girolami; G Molaro; M Lazzarin; R Scarpa; A Brunetti
Journal:  Br J Haematol       Date:  1970-08       Impact factor: 6.998

8.  Observations on hemophilia, parahemophilia, and coexistent hemophilia and parahemophilia; alterations in the platelets and the thromboplastin generation test.

Authors:  R H SEIBERT; A MARGOLIUS; O D RATNOFF
Journal:  J Lab Clin Med       Date:  1958-09

9.  [Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers].

Authors:  J OERI; M MATTER; H ISENSCHMID; F HAUSER; F KOLLER
Journal:  Bibl Paediatr       Date:  1954

10.  Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor.

Authors:  T S Zimmerman; O D Ratnoff; A E Powell
Journal:  J Clin Invest       Date:  1971-01       Impact factor: 14.808
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  5 in total

1.  The effect of heparin on platelet aggregation by common inductors and by ristocetin in congenital bleeding disorders due to factor VIII or fibrinogen defects.

Authors:  A Girolami; L De Marco; L Virgolini; R Peruffo; F Fabris
Journal:  Blut       Date:  1975-10

2.  An immunological investigation of factor VIII associated antigen in combined factor V and factor VIII deficiency.

Authors:  A Girolami; N Borsato; G Patrassi; A Sticchi
Journal:  Blut       Date:  1976-08

3.  Additional factor XII (Hageman factor) deficiency in hemophilia A and in von Willebrand syndrome.

Authors:  M Barthels; J Edel; B Liese; H E Karges
Journal:  Klin Wochenschr       Date:  1982-03

4.  Hemophilia B with associated factor VII deficiency: a distinct variant of hemophilia B with low factor VII activity and normal factor VII antigen.

Authors:  A Girolami; R Dal Bo Zanon; L De Marco; G Cappellato
Journal:  Blut       Date:  1980-04

5.  Combined deficiency of factor V and factor VIII. A report of another case.

Authors:  A Girolami; N Violante; G Cella; G Patrassi
Journal:  Blut       Date:  1976-06
  5 in total

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