228 related articles for article (PubMed ID: 31515786)
21. A family study of congenital dysfibrinogenemia caused by a novel mutation in the FGA gene: A case report.
Qiao Y; Zhang Q; Xu P; Deng Y
Open Med (Wars); 2020; 15(1):769-773. PubMed ID: 33336034
[TBL] [Abstract][Full Text] [Related]
22. [Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
Liu JX; Wang CJ; Dai JH; Zhang MX; Lyu B; Jiang B
Zhonghua Nei Ke Za Zhi; 2022 Feb; 61(2):172-176. PubMed ID: 35090252
[No Abstract] [Full Text] [Related]
23. Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.
Li S; Wang M; Li X; Xu Q; Liu S; Luo S; Chen Y
Hamostaseologie; 2020 Dec; 40(5):642-648. PubMed ID: 33374030
[TBL] [Abstract][Full Text] [Related]
24. [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]
25. A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report.
Cai R; Li Y; Wang W; Gao X; Liu M; Diao Y; Tang Y; Feng Q
Medicine (Baltimore); 2018 Oct; 97(40):e12697. PubMed ID: 30290666
[TBL] [Abstract][Full Text] [Related]
26. [Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
Wang X; Yao Y; Lin S; Wang J; Shu K; Ai X; Jiang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun; 39(6):587-591. PubMed ID: 35773760
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
Amri Y; Toumi Nel H; Hadj Fredj S; de Moerloose P
Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
Xu XC; Zhou RF; Wu JS; Fang Y; Wang XF; Zhai ZM; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):137-9. PubMed ID: 15946523
[TBL] [Abstract][Full Text] [Related]
31. Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.
Woo HI; Park IA; Lee KO; Kim SH; Kim HJ
Blood Coagul Fibrinolysis; 2012 Jul; 23(5):355-8. PubMed ID: 22576285
[TBL] [Abstract][Full Text] [Related]
32. A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia.
Wu S; Wang Z; Dong N; Bai X; Ruan C
Blood Coagul Fibrinolysis; 2005 Apr; 16(3):221-6. PubMed ID: 15795544
[TBL] [Abstract][Full Text] [Related]
33. [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]
34. Combined Congenital Hypodysfibrinogemia and Factor XI Deficiency in a Chinese Family.
Peng Y; Nie L; Qin C; Wan L; Zhou P
Acta Haematol; 2020; 143(5):472-477. PubMed ID: 31982874
[TBL] [Abstract][Full Text] [Related]
35. [Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
Luo J; Duan SR; Wang H
Sichuan Da Xue Xue Bao Yi Xue Ban; 2022 Jan; 53(1):171-174. PubMed ID: 35048620
[TBL] [Abstract][Full Text] [Related]
36. Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia.
Spena S; Asselta R; Platé M; Castaman G; Duga S; Tenchini ML
Br J Haematol; 2007 Oct; 139(1):128-32. PubMed ID: 17854317
[TBL] [Abstract][Full Text] [Related]
37. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
Neerman-Arbez M
Ann N Y Acad Sci; 2001; 936():496-508. PubMed ID: 11460507
[TBL] [Abstract][Full Text] [Related]
38. [Identification of compound heterozygous mutations of F11 gene in a pedigree affected with heriditary coagulation factor XI deficiency].
Liu M; Li X; Zhou X; Jin Y; Yang L; Pan J; Su K; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Apr; 36(4):363-367. PubMed ID: 30950027
[TBL] [Abstract][Full Text] [Related]
39. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
Neerman-Arbez M; de Moerloose P; Honsberger A; Parlier G; Arnuti B; Biron C; Borg JY; Eber S; Meili E; Peter-Salonen K; Ripoll L; Vervel C; d'Oiron R; Staeger P; Antonarakis SE; Morris MA
Hum Genet; 2001 Mar; 108(3):237-40. PubMed ID: 11354637
[TBL] [Abstract][Full Text] [Related]
40. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
Tavasoli B; Safa M; Dorgalaleh A; Ghasemi JB; Rezaei Makhouri F; Rezvani MR; Ahmadi A; Tabibian S; Jazebi M; Baghaipour MR; Zaker F
Int J Lab Hematol; 2020 Oct; 42(5):619-627. PubMed ID: 32639687
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
