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.
2. Fibrinogen Milano IV, another case of congenital dysfibrinogenemia with an abnormal fibrinopeptide A release (A alpha 16 Arg----His). Bögli C; Hofer A; Baudo F; Redaelli R; Furlan M Haemostasis; 1992; 22(1):7-11. PubMed ID: 1521828 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. Fibrinogen St. Gallen I (gamma 292 Gly--> Val): evidence for structural alterations causing defective polymerization and fibrinogenolysis. Stucki B; Schmutz P; Schmid L; Haeberli A; Lämmle B; Furlan M Thromb Haemost; 1999 Feb; 81(2):268-74. PubMed ID: 10064005 [TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release. Yan J; Luo M; Cheng P; Liao L; Deng X; Deng D; Lin F Int J Hematol; 2017 Apr; 105(4):506-514. PubMed ID: 27933517 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A'. Vorjohann S; Fish RJ; Biron-Andréani C; Nagaswami C; Weisel JW; Boulot P; Reyftmann L; de Moerloose P; Neerman-Arbez M Thromb Haemost; 2010 Nov; 104(5):990-7. PubMed ID: 20806111 [TBL] [Abstract][Full Text] [Related]
8. Fibrinogen Šumperk II: dysfibrinogenemia in an individual with two coding mutations. Kotlín R; Suttnar J; Cápová I; Hrachovinová I; Urbánková M; Dyr JE Am J Hematol; 2012 May; 87(5):555-7. PubMed ID: 22407772 [TBL] [Abstract][Full Text] [Related]
9. Paris I dysfibrinogenemia: a point mutation in intron 8 results in insertion of a 15 amino acid sequence in the fibrinogen gamma-chain. Rosenberg JB; Newman PJ; Mosesson MW; Guillin MC; Amrani DL Thromb Haemost; 1993 Mar; 69(3):217-20. PubMed ID: 8470043 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Familial hypofibrinogenaemia associated with heterozygous substitution of a conserved arginine residue; Bbeta255 Arg-->His (Fibrinogen Merivale). Maghzal GJ; Brennan SO; Fellowes AP; Spearing R; George PM Biochim Biophys Acta; 2003 Feb; 1645(2):146-51. PubMed ID: 12573244 [TBL] [Abstract][Full Text] [Related]
12. Fibrinogen Seattle II: congenital dysfibrinogenemia with an Arg (A alpha 16)----his substitution. Ebert RF; Schreiler WE; Bell WR Thromb Res; 1986 Jul; 43(1):7-13. PubMed ID: 3726812 [TBL] [Abstract][Full Text] [Related]
13. Fibrinogen Melbourne: a novel congenital hypodysfibrinogenemia caused by γ326Cys-Phe in the fibrinogen γ chain, presenting as massive splanchnic venous thrombosis. Cheah CY; Brennan SO; Kennedy H; Januszewicz EH; Maxwell E; Burbury K Blood Coagul Fibrinolysis; 2012 Sep; 23(6):563-5. PubMed ID: 22760446 [TBL] [Abstract][Full Text] [Related]
14. A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene. Iida H; Ishii E; Nakahara M; Urata M; Wakiyama M; Kurihara M; Watanabe K; Kai T; Ihara K; Kinoshita S; Hamasaki N Thromb Haemost; 2000 Jul; 84(1):49-53. PubMed ID: 10928469 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. [Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen]. Jiang L; Zhang Q; Xu W; Zhang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):812-814. PubMed ID: 30512152 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]