289 related articles for article (PubMed ID: 22967385)
1. [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]
2. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
Fang Y; Wang X; Qi H; Wu W; Ding Q; Dai J; Zhou R; Wang W; Xie S; Wang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):201-3. PubMed ID: 15793786
[TBL] [Abstract][Full Text] [Related]
3. [Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].
Ouyang Q; Ding QL; Huang DD; Xu GQ; Zhang LW; Dai J; Lu YL; Wang XF; Xi XD; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2011 Mar; 32(3):153-7. PubMed ID: 21535951
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. [Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
Jiang M; Wang X; Shu K; Jiang W; Huang Y; Lin Y; Li S; Hu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):134-9. PubMed ID: 24711018
[TBL] [Abstract][Full Text] [Related]
7. [Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.].
Zhao XJ; Wang ZY; Jiang MH; Zhang W; Cao LJ; Ma ZN; Dong NZ; Bai X; Yu ZQ; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2010 Mar; 31(3):154-6. PubMed ID: 20510102
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. [Pathogenesis study of inherited dysfibrinogenemia].
Liao Z; Xu S; Tang H; Xie Y; Duan X; Liu C; Cheng Y; Chen Y; Wang D; Luo M; Tao Z
Zhonghua Yi Xue Za Zhi; 2014 Mar; 94(10):742-6. PubMed ID: 24844956
[TBL] [Abstract][Full Text] [Related]
11. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
Fang Y; Dai BT; Wang XF; Fu QH; Dai J; Xie F; Cai XH; Wang HL; Wang ZY
Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
[TBL] [Abstract][Full Text] [Related]
12. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
Hua B; Li K; Lee A; Poon MC; Zhao Y
Haemophilia; 2015 Nov; 21(6):846-51. PubMed ID: 25982359
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
Fang Y; Wang HL; Wang XF; Fu QH; Wang WB; Xie S; Zhou RF; Dai J; Wang ZY
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec; 13(6):1086-9. PubMed ID: 16403286
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
Xue F; Ge J; Gu DS; DU WT; Sui T; Zhao HF; Zhang L; Yang RC
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug; 17(4):1021-5. PubMed ID: 19698251
[TBL] [Abstract][Full Text] [Related]
18. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
Zhang J; Zhao XJ; Wang ZY; Yu ZQ; Cao LJ; Ma ZN; Zhang J; Zhang W; Bai X; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):751-6. PubMed ID: 24103871
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].
Zhu L; Zhao M; Cheng X; Yu D; Li X; Xu F; Wang J; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):179-183. PubMed ID: 29652987
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
