Literature DB >> 418829

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency.

A Girolami, S Coccheri, G Palareti, M Poggi, A Burul, G Cappellato.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1978        PMID： 418829

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


× No keyword cloud information.
  6 in total

1.  Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento).

Authors:  A Girolami; M G Cappellato; M A Vicarioto; S Casonato; F Marafioti
Journal:  Blut       Date:  1986-01

2.  Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease.

Authors:  A Girolami; F Fabris; G Cappellato; L Sainati; G Boeri
Journal:  Blut       Date:  1983-08

3.  Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.

Authors:  H Iwahana; K Yoshimoto; T Shigekiyo; A Shirakami; S Saito; M Itakura
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

4.  Demonstration of a double hereditary pattern for congenital afibrinogenemia.

Authors:  A Girolami; G Cappellato; G Falezza; G B Gabrielli; C Vianello
Journal:  Blut       Date:  1981-10

5.  An immunological study of prothrombin in liver cirrhosis.

Authors:  A Girolami; G Patrassi; G Cappellato; V Quaino
Journal:  Blut       Date:  1980-07

6.  Identification of a congenital dysthrombin, thrombin Quick.

Authors:  R A Henriksen; W G Owen; M E Nesheim; K G Mann
Journal:  J Clin Invest       Date:  1980-11       Impact factor: 14.808
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.