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22. Fibrinogen Milano XII: a dysfunctional variant containing 2 amino acid substitutions, Aalpha R16C and gamma G165R. Bolliger-Stucki B; Lord ST; Furlan M Blood; 2001 Jul; 98(2):351-7. PubMed ID: 11435303 [TBL] [Abstract][Full Text] [Related]
23. Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen. Seydewitz HH; Gram J; Bruhn HD; Witt I Blood Coagul Fibrinolysis; 1991 Aug; 2(4):501-6. PubMed ID: 1768762 [TBL] [Abstract][Full Text] [Related]
24. Fibrinogen Magdeburg I: a novel variant of human fibrinogen with an amino acid exchange in the fibrinopeptide A (Aalpha 9, Leu-->Pro). Meyer M; Kutscher G; Stürzebecher J; Riesener G; Lutze G Thromb Res; 2003 Jan; 109(2-3):145-51. PubMed ID: 12706644 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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 [TBL] [Abstract][Full Text] [Related]
27. Fibrinogen Marburg: a homozygous case of dysfibrinogenemia, lacking amino acids A alpha 461-610 (Lys 461 AAA-->stop TAA). Koopman J; Haverkate F; Grimbergen J; Egbring R; Lord ST Blood; 1992 Oct; 80(8):1972-9. PubMed ID: 1391954 [TBL] [Abstract][Full Text] [Related]
28. Fibrinogen Osaka IV: a congenital dysfibrinogenemia found in a patient originally reported in relation to surgery, now defined to have an A alpha arginine-16 to histidine substitution. Yamazumi K; Terukina S; Matsuda M; Kanbayashi J; Sakon M; Tsujinaka T Surg Today; 1993; 23(1):45-50. PubMed ID: 8461606 [TBL] [Abstract][Full Text] [Related]
29. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His. Luo M; Deng D; Xiang L; Cheng P; Liao L; Deng X; Yan J; Lin F Medicine (Baltimore); 2016 Sep; 95(39):e4864. PubMed ID: 27684817 [TBL] [Abstract][Full Text] [Related]
30. Novel structure elucidation strategy for genetically abnormal fibrinogens with incomplete fibrinopeptide release as applied to fibrinogen Schwarzach. Henschen A; Kehl M; Deutsch E Hoppe Seylers Z Physiol Chem; 1983 Dec; 364(12):1747-51. PubMed ID: 6667926 [TBL] [Abstract][Full Text] [Related]
31. Fibrinogen Matsumoto V: a variant with Aalpha19 Arg-->Gly (AGG-->GGG). Comparison between fibrin polymerization stimulated by thrombin or reptilase and fibrin monomer polymerization. Tanaka H; Terasawa F; Ito T; Tokunaga S; Ishida F; Kitano K; Kiyosawa K; Okumura N Thromb Haemost; 2001 Jan; 85(1):108-13. PubMed ID: 11204560 [TBL] [Abstract][Full Text] [Related]
32. Fibrinogen Kawaguchi: an abnormal fibrinogen characterized by defective release of fibrinopeptide A. Matsuda M; Saeki E; Kasamatsu A; Nakamikawa C; Manabe S; Samejima Y Thromb Res; 1985 Feb; 37(3):379-90. PubMed ID: 3992527 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. ["Fibrinogen Kawaguchi": a hereditary dysfibrinogenemia characterized by defective release of fibrinopeptide A associated with altered polymerization of fibrin monomers]. Saeki E; Matsuda M; Ichinose A; Samejima Y; Kasamatsu A; Ara R; Mitsuno K; Kihara T; Hara Y Nihon Ketsueki Gakkai Zasshi; 1985 Aug; 48(5):1229-35. PubMed ID: 4072586 [No Abstract] [Full Text] [Related]
35. A new congenital abnormal fibrinogen Ise characterized by the replacement of B beta glycine-15 by cysteine. Yoshida N; Wada H; Morita K; Hirata H; Matsuda M; Yamazumi K; Asakura S; Shirakawa S Blood; 1991 May; 77(9):1958-63. PubMed ID: 2018836 [TBL] [Abstract][Full Text] [Related]
36. Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a". Lounes KC; Soria C; Mirshahi SS; Desvignes P; Mirshahi M; Bertrand O; Bonnet P; Koopman J; Soria J Blood; 2000 Nov; 96(10):3473-9. PubMed ID: 11071644 [TBL] [Abstract][Full Text] [Related]
38. Thrombin-induced fibrinopeptide release from a fibrinogen variant (fibrinogen Sydney I) with an Aalpha Arg-16----His substitution. Southan C; Lane DA; Bode W; Henschen A Eur J Biochem; 1985 Mar; 147(3):593-600. PubMed ID: 3979390 [TBL] [Abstract][Full Text] [Related]
39. Fibrinogen Petoskey, a dysfibrinogenemia characterized by replacement of Arg-A alpha 16 by a histidyl residue. Evidence for thrombin-catalyzed hydrolysis at a histidyl residue. Higgins DL; Shafer JA J Biol Chem; 1981 Dec; 256(23):12013-7. PubMed ID: 7298640 [No Abstract] [Full Text] [Related]
40. Fibrinogen Aarhus--a new case of dysfibrinogenemia. Hessel B; Stenbjerg S; Dyr J; Kudryk B; Therkildsen L; Blombäck B Thromb Res; 1986 Apr; 42(1):21-37. PubMed ID: 2939591 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]