Literature DB >> 13575936

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

R H SEIBERT, A MARGOLIUS, O D RATNOFF.   

Abstract

Entities:  

Keywords:  HEMOPHILIA/case reports; HEMORRHAGIC DIATHESIS/complications

Mesh：

Substances：

Year:  1958        PMID： 13575936

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN： 0022-2143


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  9 in total

1.  PARAPEMOPHILIA (CONGENITAL FACTOV V DEFICIENCY).

Authors:  C W BAUGH
Journal:  Can Med Assoc J       Date:  1965-05-01       Impact factor: 8.262

2.  Studies on the action of Hageman factor: evidence that activated Hageman factor in turn activates plasma thromboplastin antecedent.

Authors:  O D RATNOFF; E W DAVIE; D L MALLETT
Journal:  J Clin Invest       Date:  1961-05       Impact factor: 14.808

3.  [Blood platelets and coagulationactive plasma proteins. A short summary of their function and pathology].

Authors:  E MAMMEN; R GROSS
Journal:  Blut       Date:  1962-05

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

Authors:  A Girolami; A Brunetti; L De Marco
Journal:  Blut       Date:  1974-01

Review 5.  Genetics of human blood coagulation.

Authors:  C B Kerr
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

6.  Familial intracranial haemorrhage due to factor V deficiency.

Authors:  R S Wadia; S A Sangle; S Kripalaney; M Bafna; S R Karve
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-03       Impact factor: 10.154

7.  Studies on the purification of antihemophilic factor (factor 8. I. Precipitation of antihemophilic factor by concanavalin A.

Authors:  L Kass; O D Ratnoff; M A Leon
Journal:  J Clin Invest       Date:  1969-02       Impact factor: 14.808

8.  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

9.  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
  9 in total

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