Literature DB >> 13569427

[A new congenital coagulation defect; Stuart factor defect].

F BACHMANN, F DUCKERT, P FLUCKIGER, W HITZIG, F KOLLER.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS/case reports; INFANT, NEWBORN/diseases

Mesh：

Substances：

Year:  1958        PMID： 13569427

Source DB:  PubMed          Journal:  Thromb Diath Haemorrh        ISSN： 0340-5338


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  8 in total

1.  [CONGENITAL STEWART-PROWER FACTOR (FACTOR X) DEFICIENCY].

Authors:  F HOLZKNECHT
Journal:  Klin Wochenschr       Date:  1965-01-15

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.  [Differential diagnosis of congenital Stuart factor deficiency].

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

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

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

5.  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

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

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

7.  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

8.  Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency.

Authors:  C de Sousa; T Clark; A Bradshaw
Journal:  Arch Dis Child       Date:  1988-10       Impact factor: 3.791
  8 in total

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