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 *

180 related articles for article (PubMed ID: 7242717)

  • 1. [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]  

  • 2. Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta Gly414Ser), and Brno (gammaArg275His).
    Kotlín R; Reicheltová Z; Sobotková A; Suttnar J; Salaj P; Pospísilová D; Smejkal P; Chrastinová L; Dyr JE
    Thromb Haemost; 2008 Dec; 100(6):1199-200. PubMed ID: 19132250
    [No Abstract]   [Full Text] [Related]  

  • 3. [A family with hereditary hypofibrinogenemia].
    Pfluger N; Gehrig D
    Schweiz Med Wochenschr; 1977 Oct; 107(41):1454-5. PubMed ID: 918595
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
    Castaman G; Giacomelli SH; Duga S; Rodeghiero F
    Haemophilia; 2008 May; 14(3):630-3. PubMed ID: 18393984
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F; Samama M
    Thromb Haemost; 1995 Jan; 73(1):151-61. PubMed ID: 7740487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].
    Jiang LL; Wang XF; Ding QL; Xu GQ; Zhang LW; Dai J; Lu YL; Xi XD; Wang HL
    Zhonghua Xue Ye Xue Za Zhi; 2012 Jun; 33(6):475-9. PubMed ID: 22967385
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A hereditary dysfibrinogenemia: fibrinogen Awaji.
    Matsuo T; Okuno S; Mukaida T; Ueshima S; Okada K; Matsuo O
    Haemostasis; 1987; 17(1-2):89-97. PubMed ID: 3596361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Fibrinogen Magdeburg--a new hereditary dysfibrinogen].
    Lutze G; Urbahn H
    Z Med Lab Diagn; 1987; 28(7):378-84. PubMed ID: 3433890
    [No Abstract]   [Full Text] [Related]  

  • 10. A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis.
    Robert-Ebadi H; Le Querrec A; de Moerloose P; Gandon-Laloum S; Borel Derlon A; Neerman-Arbez M
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):697-9. PubMed ID: 18832913
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A nonsense mutation in FGA g.3807C-->T (p.R159X) causes afibrinogenaemia in the homozygous form.
    Marchi Cappelletti R; Tersek Y; Ruiz-Sáez A; Meyer M
    Acta Haematol; 2009; 121(4):216-7. PubMed ID: 19468208
    [No Abstract]   [Full Text] [Related]  

  • 12. Novel homozygous fibrinogen Aα chain truncation causes severe afibrinogenemia with life threatening complications in a two-year-old boy.
    Stikarová J; Blatný J; Kotlín R; Suttnar J; Zapletal O; Pimková K; Májek P; Hrachovinová I; Dyr JE
    Thromb Res; 2013 Oct; 132(4):490-2. PubMed ID: 24050829
    [No 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. [Case report of congenital afibrinogenemia].
    Leeners JV; Mossakowski J; Kayser S
    Klin Padiatr; 1995; 207(1):34-5. PubMed ID: 7885016
    [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. A novel fibrinogen variant: dysfibrinogenemia associated with γAsp185Asn substitution.
    Zhou N; Xu P; Zhou M; Xu Y; Li P; Chen B; Ouyang J; Zhou R
    J Thromb Thrombolysis; 2017 Jul; 44(1):139-144. PubMed ID: 28425010
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional characterisation of plasma fibrin clots in Polish carriers of fibrinogen gammaArg275His mutation (fibrinogen Zabrze).
    Undas A; Pastuszczak M; Iwaniec T; Kapelak K; Neerman-Arbez M
    Thromb Haemost; 2010 Aug; 104(2):415-7. PubMed ID: 20508898
    [No Abstract]   [Full Text] [Related]  

  • 18. Congenital hypofibrinogenemia: a distinct entity? Report of three cases in the same family.
    Capel P; Dedrie J; Detrain C; Rauis M; Fondu P
    Acta Clin Belg; 1987; 42(5):342-6. PubMed ID: 3425121
    [No Abstract]   [Full Text] [Related]  

  • 19. Fibrinogen Adelaide: a familial hypodysfibrinogenaemia associated with abnormal alpha chains.
    Exner T; Barber S; Sage RE; Kronenberg H
    Br J Haematol; 1984 Jan; 56(1):95-106. PubMed ID: 6704329
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.