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Journal Abstract Search
132 related items for PubMed ID: 4059342
1. [A case of dysfibrinogenemia complicated by hemorrhage and thrombosis]. Ouvry PA, Vergoz D, Guenneguez H. Phlebologie; 1985; 38(3):417-20. PubMed ID: 4059342 [Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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 [Abstract] [Full Text] [Related]
6. Central venous catheter-related thrombosis after replacement therapy for intracranial bleeding in a patient with afibrinogenaemia. Matsumoto T, Wada H, Tamaru S, Sugimoto Y, Fujieda A, Yamamura K, Kobayashi T, Kaneko T, Yamaguchi M, Nobori T, Katayama N. Haemophilia; 2008 Jan; 14(1):153-6. PubMed ID: 18184261 [No Abstract] [Full Text] [Related]
7. [On hemorrhagic syndromes due to fibrinogen deficiency]. Capasso DA. Pediatria (Napoli); 1967 Dec 31; 75(6):1002-9. PubMed ID: 4895740 [No Abstract] [Full Text] [Related]
8. Recurrent VTE in a heterozygote of the fibrinogen Aα IVS4+1G>T and Aα p.Arg168Ter mutation. Berens C, Rühl H, Ivaškevičius V, Oldenburg J, Hertfelder HJ, Pötzsch B. Thromb Haemost; 2016 May 02; 115(5):1073-5. PubMed ID: 26763372 [No Abstract] [Full Text] [Related]
9. Hypofibrinogenemia, dysfibrinogenemia or hypodysfibrinogenemia?: comment on 'The dilemma of inherited dysfibrinogenemia during pregnancy'. Oo TH. Blood Coagul Fibrinolysis; 2013 Apr 02; 24(3):353-4. PubMed ID: 23518794 [No Abstract] [Full Text] [Related]
10. 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 02; 96(5):685-7. PubMed ID: 17080227 [No Abstract] [Full Text] [Related]
12. Thromboembolic events in patients with severe inherited fibrinogen deficiency. Rottenstreich A, Lask A, Schliamser L, Zivelin A, Seligsohn U, Kalish Y. J Thromb Thrombolysis; 2016 Aug 02; 42(2):261-6. PubMed ID: 26712130 [Abstract] [Full Text] [Related]
17. Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes. Simsek I, de Mazancourt P, Horellou MH, Erdem H, Pay S, Dinc A, Samama MM. Blood Coagul Fibrinolysis; 2008 Apr 02; 19(3):247-53. PubMed ID: 18388508 [Abstract] [Full Text] [Related]
18. Clinical Features and Management of Congenital Fibrinogen Deficiencies. Casini A, de Moerloose P, Neerman-Arbez M. Semin Thromb Hemost; 2016 Jun 02; 42(4):366-74. PubMed ID: 27019462 [Abstract] [Full Text] [Related]