These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 1198457)

  • 1. Proceedings: A new congenital dysfibrinogenemia with hemorrhagic diathesis (fibrinogen Montreal II).
    D'Angelo G; Lacombe M; Lemay J; Lavallée R; Bonny Y; Boileau J
    Thromb Diath Haemorrh; 1975 Nov; 34(2):570. PubMed ID: 1198457
    [No Abstract]   [Full Text] [Related]  

  • 2. Fibrinogen Montreal. A new case of congenital dysfibrinogenemia with defective aggregation of monomers.
    Lacombe M; Soria J; Soria C; D'Angelo G; Lavallee R; Bonny Y
    Thromb Diath Haemorrh; 1973 Jun; 29(3):536-46. PubMed ID: 4761822
    [No Abstract]   [Full Text] [Related]  

  • 3. Fibrinogen Troyes--fibrinogen Metz. Two new cases of congenital dysfibrinogenemia.
    Soria J; Soria C; Samama M; Poirot E; Kling C
    Thromb Diath Haemorrh; 1972 Jul; 27(3):619-33. PubMed ID: 4662617
    [No Abstract]   [Full Text] [Related]  

  • 4. Congenital dysfibrinogenemia (fibrinogen Giessen).
    Krause WH; Heene DL; Lasch HG
    Thromb Diath Haemorrh; 1973 Jun; 29(3):547-61. PubMed ID: 4761823
    [No Abstract]   [Full Text] [Related]  

  • 5. [Familial dysfibrinogenemia; fibrinogen Haarlem I and II].
    Hensen A; Brommer EJ; Gravesen M; Haverkate F
    Ned Tijdschr Geneeskd; 1981 May; 125(19):734-7. PubMed ID: 7242717
    [No Abstract]   [Full Text] [Related]  

  • 6. [Congenital and familial dysfibrinogenemia without hemorrhagic tendancy].
    Samama M; Soria J; Soria C; Bousser J
    Nouv Rev Fr Hematol; 1969; 9(6):817-32. PubMed ID: 4245042
    [No Abstract]   [Full Text] [Related]  

  • 7. Proceedings: A new case of dysfibrinogenemia, fibrinogen Marburg.
    Fuchs G; Egbring R; Havemann K
    Thromb Diath Haemorrh; 1975 Nov; 34(2):570. PubMed ID: 1198456
    [No Abstract]   [Full Text] [Related]  

  • 8. Proceedings: A new type of congenital dysfibrinogenemia (fibrinogen Tokyo) with defective stabilization of fibrin polymers.
    Samori T; Yatabe M; Ukita M; Fujimaki M; Fukutake K
    Thromb Diath Haemorrh; 1975 Sep; 34(1):329. PubMed ID: 1188745
    [No Abstract]   [Full Text] [Related]  

  • 9. [Life-long hemorrhagic diathesis in a young man with unclottable global coagulation tests--congenital afibrinogenemia].
    Peter K; Furlan M; Lämmle B
    Ther Umsch; 1999 Sep; 56(9):516-8. PubMed ID: 10517123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial dysfibrinogenemia--"Detroit fibrinogen"].
    Mammen EF; Prasad AS
    Verh Dtsch Ges Inn Med; 1968; 74():140-4. PubMed ID: 5714299
    [No Abstract]   [Full Text] [Related]  

  • 11. Fibrinogen Vicenza and Genova II: two new cases of congenital dysfibrinogenemia with isolated defect of fibrin monomer polymerization and inhibitory activity on normal coagulation.
    Rodeghiero F; Castaman GC; Dal Belin Peruffo A; Dini E; Galletti A; Barone E; Gastaldi G
    Thromb Haemost; 1987 Jun; 57(3):252-8. PubMed ID: 2958952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Fang Y; Wang X; Qi H; Wu W; Ding Q; Dai J; Zhou R; Wang W; Xie S; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):201-3. PubMed ID: 15793786
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
    Kotlín R; Chytilová M; Suttnar J; Riedel T; Salaj P; Blatný J; Santrůcek J; Klener P; Dyr JE
    Thromb Res; 2007; 121(1):75-84. PubMed ID: 17408725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital fibrinogen disorders.
    de Moerloose P; Neerman-Arbez M
    Semin Thromb Hemost; 2009 Jun; 35(4):356-66. PubMed ID: 19598064
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Fibrinogen Bern II: hereditary fibrinogen variant with amino acid substitution of arginine replaced by histidine in position 16 of the A alpha chain].
    Rupp C; Sievi R; Furlan M; Beck EA
    Schweiz Med Wochenschr; 1983 Oct; 113(40):1460-2. PubMed ID: 6648427
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital hypofibrinogenemia and recurrent placental abruption.
    Ness PM; Budzynski AZ; Olexa SA; Rodvien R
    Obstet Gynecol; 1983 Apr; 61(4):519-23. PubMed ID: 6828283
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Different sensitivity of von Clauss reagents for the diagnosis of dysfibrinogenemia.
    Vasse M; Francois D; Van Dreden P; de Mazancourt P
    Eur J Haematol; 2020 Jan; 104(1):70-71. PubMed ID: 31583746
    [No Abstract]   [Full Text] [Related]  

  • 18. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R; Cappucci F; Pisanelli D; Perricone F; Papa ML; Santoro R; Grandone E; Margaglione M
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital dysfibrinogenemia.
    Rupp C; Beck EA
    Curr Probl Clin Biochem; 1984; 14():65-130. PubMed ID: 6150812
    [No Abstract]   [Full Text] [Related]  

  • 20. Studies on a family with dysfibrinogenemia.
    Mammen EF; Prasad AS; Au CC
    Thromb Diath Haemorrh; 1968 Jul; 19(3):03-4. PubMed ID: 5708123
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.