257 related articles for article (PubMed ID: 22732251)
41. [Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
Wang X; Yang X; Yang W; Shu K; Li F; Liu J; Zhang Z; Li S; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):901-904. PubMed ID: 31515786
[TBL] [Abstract][Full Text] [Related]
42. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population.
Özkan DT; Sarper N; Akar N
Acta Haematol; 2020; 143(6):529-532. PubMed ID: 32289806
[TBL] [Abstract][Full Text] [Related]
43. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
Wypasek E; Klukowska A; Zdziarska J; Zawilska K; Treliński J; Iwaniec T; Mital A; Pietrys D; Sydor W; Neerman-Arbez M; Undas A
Thromb Res; 2019 Oct; 182():133-140. PubMed ID: 31479941
[TBL] [Abstract][Full Text] [Related]
44. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.
Kotlín R; Blažek B; Suttnar J; Malý M; Kvasnička J; Dyr JE
Blood Coagul Fibrinolysis; 2010 Oct; 21(7):640-8. PubMed ID: 20829681
[TBL] [Abstract][Full Text] [Related]
45. Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.
Sheen CR; Brennan SO; Jabado N; George PM
Thromb Haemost; 2006 Aug; 96(2):231-2. PubMed ID: 16894470
[No Abstract] [Full Text] [Related]
46. Diagnosis of congenital fibrinogen disorders.
Lebreton A; Casini A
Ann Biol Clin (Paris); 2016 Aug; 74(4):405-12. PubMed ID: 27492693
[TBL] [Abstract][Full Text] [Related]
47. In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes.
Stroka D; Keogh A; Vu D; Fort A; Stoffel MH; Kühni-Boghenbor K; Furer C; Banz V; Demarmels Biasiutti F; Lämmle B; Candinas D; Neerman-Arbez M
J Thromb Haemost; 2014 Nov; 12(11):1874-9. PubMed ID: 25163824
[TBL] [Abstract][Full Text] [Related]
48. Congenital fibrinogen disorder caused by digenic mutations of the
Wang X; Tang N; Shen N; Lu Y; Li D
Hematology; 2020 Dec; 25(1):145-148. PubMed ID: 32228225
[No Abstract] [Full Text] [Related]
49. Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
Mukaddam A; Patil R; Jadli A; Chandrakala S; Ghosh K; Shetty S
Am J Clin Pathol; 2015 May; 143(5):755-7. PubMed ID: 25873512
[TBL] [Abstract][Full Text] [Related]
50. A case of afibrinogenemia associated with A-alpha chain gene compound heterozygosity (HUMFIBRA c.[4110delA]+[3200+1G>T]).
Angles-Cano E; Mathonnet F; Dreyfus M; Claeyssens S; de Mazancourt P
Blood Coagul Fibrinolysis; 2007 Jan; 18(1):73-5. PubMed ID: 17179831
[TBL] [Abstract][Full Text] [Related]
51. Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient.
Platé M; Asselta R; Peyvandi F; Tenchini ML; Duga S
Biochim Biophys Acta; 2007 Jul; 1772(7):781-7. PubMed ID: 17531448
[TBL] [Abstract][Full Text] [Related]
52. Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis.
Tajdar M; Orlando C; Casini A; Herpol M; De Bisschop B; Govaert P; Neerman-Arbez M; Jochmans K
Thromb Res; 2018 Mar; 163():185-189. PubMed ID: 29122299
[TBL] [Abstract][Full Text] [Related]
53. [Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].
Zhang YL; Liu SY; Zhang ZL; Tao XY; Peng XX; Kong YY
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1514-1517. PubMed ID: 29070135
[TBL] [Abstract][Full Text] [Related]
54. Mutational Epidemiology of Congenital Fibrinogen Disorders.
Casini A; Blondon M; Tintillier V; Goodyer M; Sezgin ME; Gunes AM; Hanss M; de Moerloose P; Neerman-Arbez M
Thromb Haemost; 2018 Nov; 118(11):1867-1874. PubMed ID: 30332696
[TBL] [Abstract][Full Text] [Related]
55. Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.
Zhu L; Wang Y; Zhao M; Hao X; Xie H; Xie Y; Wang M; Ding H
Blood Coagul Fibrinolysis; 2014 Dec; 25(8):894-7. PubMed ID: 24914742
[TBL] [Abstract][Full Text] [Related]
56. Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature.
Zdziarska J; Wypasek E; Iwaniec T; Vilar R; Neerman-Arbez M; Undas A
Haemophilia; 2021 Jan; 27(1):26-32. PubMed ID: 33245842
[TBL] [Abstract][Full Text] [Related]
57. Homozygous truncation of the fibrinogen A alpha chain within the coiled coil causes congenital afibrinogenemia.
Fellowes AP; Brennan SO; Holme R; Stormorken H; Brosstad FR; George PM
Blood; 2000 Jul; 96(2):773-5. PubMed ID: 10887149
[TBL] [Abstract][Full Text] [Related]
58. An
Mischke R; Metzger J; Distl O
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356081
[TBL] [Abstract][Full Text] [Related]
59. A novel mutation in exon 2 of FGB caused by c.221G>T
Shlebak AA; Katsarou AD; Adams G; Fernando F
J Thromb Thrombolysis; 2017 Feb; 43(2):263-270. PubMed ID: 27812779
[TBL] [Abstract][Full Text] [Related]
60. Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
Vu D; Di Sanza C; Caille D; de Moerloose P; Scheib H; Meda P; Neerman-Arbez M
Hum Mol Genet; 2005 Nov; 14(21):3271-80. PubMed ID: 16195396
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
