228 related articles for article (PubMed ID: 24103874)
1. [Analysis of a hereditary protein C deficient consanguineous pedigree caused by Phe139Val homozygous mutation].
Yang LH; Zhu LQ; Wang YY; Xie HX; Xie YS; Jin YH; Wang MS; Chen BC; Yang XL
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):767-70. PubMed ID: 24103874
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].
Yang LH; Zhu LQ; Yang XO; Wang MS; Li J; Chen BC; Jin YH; Zhang Z; Zheng FX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):515-8. PubMed ID: 23042384
[TBL] [Abstract][Full Text] [Related]
3. [Analysis of a consanguineous pedigree featuring hereditary coagulation factor Ⅴ deficiency].
Xie YS; Zhang Y; Zhu LQ; Jin YH; Yang LH; Xie HX; Wang MS; Yang XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):161-4. PubMed ID: 23568726
[TBL] [Abstract][Full Text] [Related]
4. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
[TBL] [Abstract][Full Text] [Related]
5. [Analysis of an hereditary coagulation factor XII deficiency in a consanguineous pedigree].
Zhang Y; Xie HX; Wang MS; Jin YH; Xie YS; Zheng FX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):666-9. PubMed ID: 22161101
[TBL] [Abstract][Full Text] [Related]
6. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
Zhou RF; Wang HL; Fu QH; Wang WB; Wu WM; Ding QL; Xie S; Hu YQ; Wang XF; Wang ZY
Zhonghua Yi Xue Za Zhi; 2003 Oct; 83(19):1694-7. PubMed ID: 14642106
[TBL] [Abstract][Full Text] [Related]
7. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
Jin Y; Hao X; Cheng X; Yang L; Chen Y; Xie H; Wang Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):296-9. PubMed ID: 27264807
[TBL] [Abstract][Full Text] [Related]
8. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
Yang LH; Wang MS; Zheng FX; Li J; Chen Y; Jin YH; Xie HX; Yang XL; Chen BC
Genet Mol Res; 2014 Apr; 13(2):2969-77. PubMed ID: 24782131
[TBL] [Abstract][Full Text] [Related]
9. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
Yang LH; Zheng FX; Chen Y; Jin YH; Zhang Z; Xie HX; Yang XL; Wang MS; Chen BC
Blood Coagul Fibrinolysis; 2014 Dec; 25(8):824-30. PubMed ID: 24911457
[TBL] [Abstract][Full Text] [Related]
10. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
Jin Y; Wang M; Wang Y; Yang X; Yang L; Xie Y; Xie H; Zhu L; Yu F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
[TBL] [Abstract][Full Text] [Related]
11. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
Tjeldhorn L; Sandset PM; Haugbro K; Skretting G
Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency].
Yang L; Jin Y; Yang T; Chen X; Zhu L; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):10-14. PubMed ID: 28186585
[TBL] [Abstract][Full Text] [Related]
13. [Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene].
Liu S; Yu F; Luo S; Li X; Jin Y; Yang L; Zhou X; Zhang H; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1108-1112. PubMed ID: 32924112
[TBL] [Abstract][Full Text] [Related]
14. [A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C].
Ye X; Liu X; Feng Y; Ding Q; Zhou X; Wang X
Nan Fang Yi Ke Da Xue Xue Bao; 2012 Jan; 32(1):109-12. PubMed ID: 22366017
[TBL] [Abstract][Full Text] [Related]
15. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
Liu L; Guo WR; He LS; Mu H; Jiang Y; Huang FQ; Li JZ
Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):115-8. PubMed ID: 12697119
[TBL] [Abstract][Full Text] [Related]
16. [Phenotypic detection and structure analysis of a PC missense mutation (Met406Ile) resulted in venous thromboembolism].
Zhang L; Deng HY; Xie J; Gu Y; Shen W; Zhang JW
Zhonghua Yi Xue Za Zhi; 2013 Aug; 93(29):2275-8. PubMed ID: 24300144
[TBL] [Abstract][Full Text] [Related]
17. Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation.
Yu T; Dai J; Liu H; Wang J; Ding Q; Wang H; Wang X; Fu Q
Pathology; 2012 Jun; 44(4):348-53. PubMed ID: 22531345
[TBL] [Abstract][Full Text] [Related]
18. [Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
Yang L; Jin S; Ji W; Cheng X; Li X; Jin Y; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):69-73. PubMed ID: 29419864
[TBL] [Abstract][Full Text] [Related]
19. Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family.
Cafolla A; D'Andrea G; Baldacci E; Margaglione M; Mazzucconi MG; Foà R
Eur J Haematol; 2012 Apr; 88(4):336-9. PubMed ID: 22168450
[TBL] [Abstract][Full Text] [Related]
20. [Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency].
Yang L; Hao X; Wang Y; Xie H; Jin Y; Zhu L; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):343-7. PubMed ID: 26037346
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]