Similar articles for PMID: 22008904

Year	Number of Results
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1

Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.

Livnat T, Shenkman B, Kenet G, Tamarin I, Gillis S, Varon D, Iijima K, Zivelin A, Salomon O. Livnat T, et al. Blood Coagul Fibrinolysis. 2011 Dec;22(8):673-9. doi: 10.1097/MBC.0b013e32834ad785. Blood Coagul Fibrinolysis. 2011. PMID: 22008904

2

Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.

Chafa O, Tagzirt M, Tapon-Bretaudière J, Reghis A, Fischer AM, LeBonniec BF. Chafa O, et al. Thromb Res. 2009 May;124(1):144-8. doi: 10.1016/j.thromres.2008.11.018. Epub 2009 Jan 10. Thromb Res. 2009. PMID: 19135706

3

Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma.

Castoldi E, Duckers C, Radu C, Spiezia L, Rossetto V, Tagariello G, Rosing J, Simioni P. Castoldi E, et al. J Thromb Haemost. 2011 May;9(5):959-68. doi: 10.1111/j.1538-7836.2011.04237.x. J Thromb Haemost. 2011. PMID: 21320286 Free article.

4

[Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].

Wang WB, Wang HL, Wang XF, Fu QH, Zhou RF, Xie S, Hu YQ, Wang ZY. Wang WB, et al. Zhonghua Xue Ye Xue Za Zhi. 2004 Sep;25(9):519-22. Zhonghua Xue Ye Xue Za Zhi. 2004. PMID: 15569527 Chinese.

5

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.

Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, George B, Chandy M, Srivastava A. Jayandharan G, et al. J Thromb Haemost. 2005 Jul;3(7):1482-7. doi: 10.1111/j.1538-7836.2005.01339.x. Epub 2005 May 9. J Thromb Haemost. 2005. PMID: 15892863 Free article.

6

Six novel missense mutations causing factor X deficiency and application of thrombin generation test.

Liang Q, Chen Q, Ding Q, Wu F, Wang X, Xi X, Wang H. Liang Q, et al. Thromb Res. 2013 Jun;131(6):554-9. doi: 10.1016/j.thromres.2013.04.014. Epub 2013 May 7. Thromb Res. 2013. PMID: 23664564

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. Jin Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):296-9. doi: 10.3760/cma.j.issn.1003-9406.2016.03.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264807 Chinese.

8

Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide.

Li M, Jin Y, Wang M, Xie Y, Ding H. Li M, et al. Clin Lab. 2016 Nov 1;62(11):2253-2256. doi: 10.7754/Clin.Lab.2016.160503. Clin Lab. 2016. PMID: 28164683

9

[Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].

Wang MS, Jin YH, Zheng FX, Xie HX, Xu PF, Niu ZZ. Wang MS, et al. Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):854-7. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 22339961 Chinese.

10

The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).

Forberg E, Huhmann I, Jimenez-Boj E, Watzke HH. Forberg E, et al. Thromb Haemost. 2000 Feb;83(2):234-8. Thromb Haemost. 2000. PMID: 10739379

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