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62. Fibrinogen Bondy: a new case of dysfibrinogenemia. Isolation of the abnormal fibrinogen molecules. Jandrot-Perrus M; Aurousseau MH; Rabiet MJ; Josso F Thromb Res; 1982 Sep; 27(6):659-70. PubMed ID: 6217586 [TBL] [Abstract][Full Text] [Related]
63. The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia. Jacquemin M; Vanlinthout I; Van Horenbeeck I; Debasse M; Toelen J; Schoeters J; Lavend'homme R; Freson K; Peerlinck K Int J Lab Hematol; 2017 Jun; 39(3):301-307. PubMed ID: 28318107 [TBL] [Abstract][Full Text] [Related]
64. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo. Margaglione M; Vecchione G; Santacroce R; D'Angelo F; Casetta B; Papa ML; Grandone E; Di Minno G Thromb Haemost; 2001 Dec; 86(6):1483-8. PubMed ID: 11776317 [TBL] [Abstract][Full Text] [Related]
65. [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]
66. Fibrinogen Milano XIII (Aalpha 19 Arg-->Gly): a dysfunctional variant with an amino acid substitution in the N-terminal polymerization site. Bolliger-Stucki B; Bucciarelli P; Lämmle B; Furlan M Thromb Res; 1999 Dec; 96(5):399-405. PubMed ID: 10605955 [No Abstract] [Full Text] [Related]
67. Fibrinogen New Britain: characterization of an A alpha Arg 16-->His variant human fibrinogen. Webb CD; Hantgan RR; Byeff PD; Owen J Blood Coagul Fibrinolysis; 1994 Apr; 5(2):233-8. PubMed ID: 8054455 [TBL] [Abstract][Full Text] [Related]
68. A novel variant fibrinogen, AαE11del, demonstrating the importance of AαE11 residue in thrombin binding. Kaido T; Yoda M; Kamijo T; Arai S; Yamauchi K; Okumura N Int J Hematol; 2021 Nov; 114(5):591-598. PubMed ID: 34333754 [TBL] [Abstract][Full Text] [Related]
69. A new dysfibrinogenemia: fibrinogen Oslo IV. Stormorken H; Brosstad F; Seim H Thromb Haemost; 1983 Apr; 49(2):120-2. PubMed ID: 6868008 [TBL] [Abstract][Full Text] [Related]
70. Dysfibrinogenaemia characterized by abnormal fibrin monomer polymerization and normal fibrinopeptide A release. Lane DA; Cuddigan B; VanRoss M; Kakkar VV Br J Haematol; 1980 Mar; 44(3):483-94. PubMed ID: 6769460 [TBL] [Abstract][Full Text] [Related]
71. Fibrinogen Manchester: identification of an abnormal fibrinopeptide A with a C-terminal arginine leads to histidine substitution. Southan C; Kehl M; Henschen A; Lane DA Br J Haematol; 1983 May; 54(1):143-51. PubMed ID: 6849832 [TBL] [Abstract][Full Text] [Related]
72. Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions. Luo M; Wei A; Xiang L; Yan J; Liao L; Deng X; Deng D; Cheng P; Lin F J Thromb Thrombolysis; 2018 Oct; 46(3):409-419. PubMed ID: 29869737 [TBL] [Abstract][Full Text] [Related]
73. [Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain]. Zhou JY; Wang XF; Ding QL; Xu GQ; Zhang LW; Dai J; Lu YL; Xi XD; Wang HL Zhonghua Xue Ye Xue Za Zhi; 2013 Mar; 34(3):190-4. PubMed ID: 23683413 [TBL] [Abstract][Full Text] [Related]
74. Molecular basis of fibrinogen Naples associated with defective thrombin binding and thrombophilia. Homozygous substitution of B beta 68 Ala----Thr. Koopman J; Haverkate F; Lord ST; Grimbergen J; Mannucci PM J Clin Invest; 1992 Jul; 90(1):238-44. PubMed ID: 1634610 [TBL] [Abstract][Full Text] [Related]
75. Congenital fibrinogen disorders with repeated thrombosis. Zhang X; Zhang C; Wang B; Chen N; Sun G; Guo X J Thromb Thrombolysis; 2020 Feb; 49(2):312-315. PubMed ID: 31542854 [TBL] [Abstract][Full Text] [Related]
76. Fibrinogen Seattle releases half the normal amount of fibrinopeptide B. Branson HE; Schmer G; Theodor I; Pirkle H Acta Haematol; 1983; 70(4):257-63. PubMed ID: 6414212 [TBL] [Abstract][Full Text] [Related]
77. Fibrinogen residue γAla341 is necessary for calcium binding and 'A-a' interactions. Park R; Ping L; Song J; Hong SY; Choi TY; Choi JR; Gorkun OV; Lord ST Thromb Haemost; 2012 May; 107(5):875-83. PubMed ID: 22437918 [TBL] [Abstract][Full Text] [Related]
78. 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 [TBL] [Abstract][Full Text] [Related]
79. Fibrinogen giessen I: a congenital homozygously expressed dysfibrinogenemia with A alpha 16 Arg----His substitution. Alving BM; Henschen AH Am J Hematol; 1987 Aug; 25(4):479-82. PubMed ID: 3618591 [TBL] [Abstract][Full Text] [Related]
80. Fibrinogen Saint-Germain I: a case of the heterozygous Aalpha GLY 12 --> VAL fibrinogen variant. Mathonnet F; Peltier JY; Detruit H; de Raucourt E; Alvarez JC; Mazmanian GM; de Mazancourt P Blood Coagul Fibrinolysis; 2002 Mar; 13(2):149-53. PubMed ID: 11914657 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]