Literature DB >> 13508021

[Congenital familial deficiency of factor VII with additional defect of thromboplastin formation].

M H HORDER.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS; THROMBOPLASTIN

Mesh：

Substances：

Year:  1958        PMID： 13508021     DOI： 10.1159/000205411

Source DB:  PubMed          Journal:  Acta Haematol        ISSN： 0001-5792            Impact factor:   2.195


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  5 in total

1.  [ACTIVATION OF BLOOD COAGULATION BY A BACTERIAL ENDOTOXIN IN PERSONS UNDER COUMARIN THERAPY].

Authors:  M H HOERDER; R MANRIQUE
Journal:  Klin Wochenschr       Date:  1965-04-01

Review 2.  [THE STUART-PROWER FACTOR: ITS COAGULATION PHYSIOLOGY AND CLINICAL SIGNIFICANCE].

Authors:  V HIEMEYER; M H HOERDER
Journal:  Klin Wochenschr       Date:  1964-11-15

3.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1958-12       Impact factor: 11.025

4.  [Differential diagnosis of congenital Stuart factor deficiency].

Authors:  M H HORDER
Journal:  Klin Wochenschr       Date:  1959-04-15

5.  [Clinical studies of familial hereditary factor VII deficiency (author's transl)].

Authors:  E Pilger; H Schenk; J Haralambus; S Sailer
Journal:  Blut       Date:  1981-05
  5 in total

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