Literature DB >> 13363738

Investigation of a haemorrhagic disease due to beta-prothromboplastin deficiency complicated by a specific inhibitor of thromboplastin formation.

P FANTL, A G MARR, R J SAWERS.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS

Mesh:

Substances:

Year:  1956        PMID: 13363738     DOI: 10.1111/imj.1956.5.3.163

Source DB:  PubMed          Journal:  Australas Ann Med        ISSN: 0571-9283


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  7 in total

1.  [Development of inhibitors following long-term substitution of human antihemophilia globulin in severe hemophilia].

Authors:  F Bläker; K Fischer; G Landbeck
Journal:  Klin Wochenschr       Date:  1967-06-15

Review 2.  Hereditary disorders of blood coagulation due to defective and deficient synthesis of protein.

Authors:  D P Jackson
Journal:  Trans Am Clin Climatol Assoc       Date:  1971

3.  Hemophilia B+ or Bm. First case reported in Italy.

Authors:  A Girolami; G Cella; G Bareggi
Journal:  Blut       Date:  1973-04

4.  Purification and characterization of an abnormal factor IX (Christmas factor) molecule. Factor IX Chapel Hill.

Authors:  K S Chung; D A Madar; J C Goldsmith; H S Kingdon; H R Roberts
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

5.  An investigation of three patients with Christmas disease due to an abnormal type of factor IX.

Authors:  K W Denson; R Biggs; P M Mannucci
Journal:  J Clin Pathol       Date:  1968-03       Impact factor: 3.411

6.  Genetic variants of hemophilia B: detection by means of a specific PTC inhibitor.

Authors:  H R Roberts; J E Grizzle; W D McLester; G D Penick
Journal:  J Clin Invest       Date:  1968-02       Impact factor: 14.808

7.  Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin.

Authors:  S S Shapiro; J Martinez; R R Holburn
Journal:  J Clin Invest       Date:  1969-12       Impact factor: 14.808

  7 in total

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