Literature DB >> 4245042

[Congenital and familial dysfibrinogenemia without hemorrhagic tendancy].

M Samama, J Soria, C Soria, J Bousser.   

Abstract

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Year:  1969        PMID： 4245042

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol        ISSN： 0029-4810


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  7 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.  Fibrinogen St. Louis: a new inherited fibrinogen variant, coincidentally associated with hemophilia A.

Authors:  L A Sherman; L W Gaston; M E Kaplan; A R Spivack
Journal:  J Clin Invest       Date:  1972-03       Impact factor: 14.808

5.  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.  Fibrinogen Bethesda: a congenital dysfibrinogenemia with delayed fibrinopeptide release.

Authors:  H R Gralnick; H M Givelber; J R Shainoff; J S Finlayson
Journal:  J Clin Invest       Date:  1971-09       Impact factor: 14.808

7.  Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Authors:  Claire-Marie Dhaenens; Frans P M Cremers; Mubeen Khan; Stéphanie S Cornelis; Marta Del Pozo-Valero; Laura Whelan; Esmee H Runhart; Ketan Mishra; Femke Bults; Yahya AlSwaiti; Alaa AlTalbishi; Elfride De Baere; Sandro Banfi; Eyal Banin; Miriam Bauwens; Tamar Ben-Yosef; Camiel J F Boon; L Ingeborgh van den Born; Sabine Defoort; Aurore Devos; Adrian Dockery; Lubica Dudakova; Ana Fakin; G Jane Farrar; Juliana Maria Ferraz Sallum; Kaoru Fujinami; Christian Gilissen; Damjan Glavač; Michael B Gorin; Jacquie Greenberg; Takaaki Hayashi; Ymkje M Hettinga; Alexander Hoischen; Carel B Hoyng; Karsten Hufendiek; Herbert Jägle; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C W Klaver; Bohdan Kousal; Tina M Lamey; Ian M MacDonald; Anna Matynia; Terri L McLaren; Marcela D Mena; Isabelle Meunier; Rianne Miller; Hadas Newman; Buhle Ntozini; Monika Oldak; Marc Pieterse; Osvaldo L Podhajcer; Bernard Puech; Raj Ramesar; Klaus Rüther; Manar Salameh; Mariana Vallim Salles; Dror Sharon; Francesca Simonelli; Georg Spital; Marloes Steehouwer; Jacek P Szaflik; Jennifer A Thompson; Caroline Thuillier; Anna M Tracewska; Martine van Zweeden; Andrea L Vincent; Xavier Zanlonghi; Petra Liskova; Heidi Stöhr; John N De Roach; Carmen Ayuso; Lisa Roberts; Bernhard H F Weber
Journal:  Genet Med       Date:  2020-04-20       Impact factor: 8.822
  7 in total

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