Literature DB >> 13313579

Congenital hemorrhagic diathesis of the prothrombin complex.

T NEWCOMB, M MATTER, L CONROY, Q B DEMARSH, C A FINCH.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS

Mesh：

Substances：

Year:  1956        PMID： 13313579     DOI： 10.1016/0002-9343(56)90163-2

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  8 in total

1.  A congenital blood-clotting anomaly resembling coumarin-induced defect.

Authors:  F NOUR-ELDIN; J F WILKINSON
Journal:  Br Med J       Date:  1959-05-02

2.  Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state.

Authors:  J B GRAHAM; E M BARROW; C HOUGIE
Journal:  J Clin Invest       Date:  1957-03       Impact factor: 14.808

3.  Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency.

Authors:  C HOUGIE; E M BARROW; J B GRAHAM
Journal:  J Clin Invest       Date:  1957-03       Impact factor: 14.808

4.  Familial haemophilia and factor VII deficiency.

Authors:  M CONSTANDOULAKIS
Journal:  J Clin Pathol       Date:  1958-09       Impact factor: 3.411

5.  [Prothrombin: a unit or complex?].

Authors:  D Voss
Journal:  Klin Wochenschr       Date:  1967-05-01

6.  [On the treatment of Factor II, VII and X deficiency with P.P.S.B].

Authors:  M Fischer; E Zweymüller
Journal:  Blut       Date:  1968-01

7.  Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives.

Authors:  R M Pauli; J B Lian; D F Mosher; J W Suttie
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

8.  Haemorrhagic diathesis in children associated with vitamin K deficiency.

Authors:  S Taj-Eldin; L al-Nouri; O Fakri
Journal:  J Clin Pathol       Date:  1967-05       Impact factor: 3.411
  8 in total

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