Literature DB >> 4947421

[A new case of Congenital and familial dysfibrinogenemia without Hemorrhagic Diathesis].

F Streiff, P Alexandre, C Vigneron, J Soria, C Soria, L Mester.   

Abstract

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Year:  1971        PMID： 4947421

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


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  6 in total

1.  Congenital dysfibrinogenemias: molecular abnormalities of fibrinogen.

Authors:  E F Mammen
Journal:  Blut       Date:  1976-10

2.  [Dysfibrinogenemia. A new case: dysfibrinogenemia Giessen III (author's transl)].

Authors:  F R Matthias; W H Krause; S Ganssert; K Mueller; H G Lasch
Journal:  Klin Wochenschr       Date:  1977-06-01

3.  Fibrinogen Philadelphia. A hereditary hypodysfibrinogenemia characterized by fibrinogen hypercatabolism.

Authors:  J Martinez; R R Holburn; S S Shapiro; A J Erslev
Journal:  J Clin Invest       Date:  1974-02       Impact factor: 14.808

4.  Abnormal sialic acid content of the dysfibrinogenemia associated with liver disease.

Authors:  J Martinez; J E Palascak; D Kwasniak
Journal:  J Clin Invest       Date:  1978-02       Impact factor: 14.808

5.  Fibrinogen Marburg a new genetic variant of fibrinogen.

Authors:  G Fuchs; R Egbring; K Havemann
Journal:  Blut       Date:  1977-02

6.  Fibrinogen Cleveland II. An abnormal fibrinogen with defective release of fibrinopeptide A.

Authors:  E D Crum; J R Shainoff; R C Graham; O D Ratnoff
Journal:  J Clin Invest       Date:  1974-05       Impact factor: 14.808
  6 in total

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