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Journal Abstract Search

458 related items for PubMed ID: 19357502

  • 1. Treatment of patients with dysfibrinogenemia and a history of abortions during pregnancy.
    Miesbach W, Galanakis D, Scharrer I.
    Blood Coagul Fibrinolysis; 2009 Jul; 20(5):366-70. PubMed ID: 19357502
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. The dilemma of inherited dysfibrinogenemia during pregnancy.
    Munoz J, Schering J, Lambing A, Neal S, Goyert G, Green PM, Hanbali A, Raman S, Kuriakose P.
    Blood Coagul Fibrinolysis; 2012 Dec; 23(8):775-7. PubMed ID: 23135383
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  • 5. Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions.
    Aygören-Pürsün E, Martinez Saguer I, Rusicke E, Louwen F, Geka F, Ivaskevicius V, Oldenburg J, Klingebiel T, Kreuz W.
    Am J Hematol; 2007 Apr; 82(4):317-20. PubMed ID: 17034026
    [Abstract] [Full Text] [Related]

  • 6. [Obstetrical management of dysfibrinogenemia with increased thrombophilia].
    Klein M, Rosen A, Kyrle P, Beck A.
    Geburtshilfe Frauenheilkd; 1992 Jul; 52(7):442-4. PubMed ID: 1499957
    [Abstract] [Full Text] [Related]

  • 7. Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects.
    Miesbach W, Scharrer I, Henschen A, Neerman-Arbez M, Spitzer S, Galanakis D.
    Blood Coagul Fibrinolysis; 2010 Jan; 21(1):35-40. PubMed ID: 19923982
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Dysfibrinogenemia during pregnancy treated successfully with fibrinogen.
    Yamanaka Y, Takeuchi K, Sugimoto M, Sato A, Nakago S, Maruo T.
    Acta Obstet Gynecol Scand; 2003 Oct; 82(10):972-3. PubMed ID: 12956852
    [No Abstract] [Full Text] [Related]

  • 10. Fibrinogen Poissy II (gammaN361K): a novel dysfibrinogenemia associated with defective polymerization and peptide B release.
    Mathonnet F, Guillon L, Detruit H, Mazmanian GM, Dreyfus M, Alvarez JC, Giudicelli Y, de Mazancourt P.
    Blood Coagul Fibrinolysis; 2003 Apr; 14(3):293-8. PubMed ID: 12695754
    [Abstract] [Full Text] [Related]

  • 11. Successful Pregnancy under Fibrinogen Substitution with Heparin and Aspirin in a Woman with Dysfibrinogenemia Revealed by Placental Abruption.
    Bouvier S, Chea M, Ripart S, Hanss M, de Mazancourt P, Gris JC.
    Thromb Haemost; 2018 Nov; 118(11):2006-2008. PubMed ID: 30296816
    [No Abstract] [Full Text] [Related]

  • 12. [Dysfibrinogenemia developed in a pregnant woman who has fibrinogen AαThr312Ala (ACT/GCT) polymorphism].
    Yamaguchi A, Taga A, Kamei S, Wada M, Fujita Y, Wada H, Fujita K.
    Rinsho Ketsueki; 2016 Jan; 57(1):31-5. PubMed ID: 26861101
    [Abstract] [Full Text] [Related]

  • 13. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 14. Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation.
    Zdziarska J, Undas A, Basa J, Iwaniec T, Skotnicki AB, de Moerloose P, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2009 Jul; 20(5):374-6. PubMed ID: 19300242
    [Abstract] [Full Text] [Related]

  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. 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
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  • 18. Fibrinogen replacement therapy for congenital fibrinogen deficiency.
    Bornikova L, Peyvandi F, Allen G, Bernstein J, Manco-Johnson MJ.
    J Thromb Haemost; 2011 Sep; 9(9):1687-704. PubMed ID: 21711446
    [Abstract] [Full Text] [Related]

  • 19. Fibrinogen Darlinghurst: hypofibrinogenaemia caused by a W253G mutation in the gamma chain in a patient with both bleeding and thrombotic complications.
    Sheen CR, Low J, Joseph J, Kotlyar E, George PM, Brennan SO.
    Thromb Haemost; 2006 Nov; 96(5):685-7. PubMed ID: 17080227
    [No Abstract] [Full Text] [Related]

  • 20. Dysfibrinogenemia associated with thrombosis and third-trimester fetal loss. A case report.
    Takala T, Oksa H, Rasi V, Tuimala R.
    J Reprod Med; 1991 May; 36(5):410-2. PubMed ID: 2061889
    [Abstract] [Full Text] [Related]

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