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Items: 1 to 20 of 103

1.

Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency.

Tajima K, Yamamoto H, Yamamoto M, Kato Y, Kato T.

Thromb Res. 2013 Jan;131(1):102-4. doi: 10.1016/j.thromres.2012.10.016. Epub 2012 Nov 20. No abstract available.

PMID:
23174622
2.

PROC c.574_576del polymorphism: a common genetic risk factor for venous thrombosis in the Chinese population.

Tang L, Lu X, Yu JM, Wang QY, Yang R, Guo T, Mei H, Hu Y.

J Thromb Haemost. 2012 Oct;10(10):2019-26. doi: 10.1111/j.1538-7836.2012.04862.x.

3.

Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.

Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K.

Thromb Haemost. 2009 Apr;101(4):785-7. No abstract available.

PMID:
19350130
4.

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. doi: 10.1097/MBC.0000000000000153.

PMID:
24911457
5.

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. doi: 10.1097/PAT.0b013e328353a218.

PMID:
22531345
6.

The protein C omega-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity.

Preston RJ, Morse C, Murden SL, Brady SK, O'Donnell JS, Mumford AD.

Br J Haematol. 2009 Mar;144(6):946-53. doi: 10.1111/j.1365-2141.2008.07550.x. Epub 2008 Dec 26.

PMID:
19133979
7.

Molecular mechanism for hereditary protein C deficiency in two Chinese families with thrombosis.

Zhou RF, Cai XH, Xie S, Wang XF, Wang HL.

J Thromb Haemost. 2006 May;4(5):1154-6. No abstract available.

8.

Mesenteric venous thrombosis in hereditary protein C deficiency with the mutation at Arg169 (CGG-TGG).

Momoi A, Komura Y, Kumon I, Tamai M, Tarumi Y, Matsubara J, Miyauchi K, Yamanouchi J, Hato T.

Intern Med. 2003 Jan;42(1):110-6.

9.

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 16;13(2):2969-77. doi: 10.4238/2014.April.16.5.

10.

[Antithrombin deficiency and thrombosis in a young child].

Kok V, Slacmeulder M, Jochmans K, Ninane J.

Arch Pediatr. 1999 Mar;6(3):279-82. French.

PMID:
10191894
11.

Unraveling the thrombophilia paradox: from hypercoagulability to the prothrombotic state.

Baglin T.

J Thromb Haemost. 2010 Feb;8(2):228-33. doi: 10.1111/j.1538-7836.2009.03702.x. Epub 2009 Nov 23.

12.

Dual genetic abnormality in the coagulation pathway as a cause of familial thrombophilia.

Khaira A, Kalra OP, Gupta A, Khaira DD.

J Assoc Physicians India. 2009 Jul;57:529-30.

PMID:
20329415
13.

A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.

Ozlu F, Kyotani M, Taskin E, Ozcan K, Kojima T, Matsushita T, Yapicioğlu H, Takagi A, Saşmaz I, Satar M, Narli N.

J Pediatr Hematol Oncol. 2008 Aug;30(8):608-11. doi: 10.1097/MPH.0b013e318179a15d.

PMID:
18799939
14.

The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.

Bovill EG, Hasstedt SJ, Callas PW, Valliere JE, Scott BT, Bauer KA, Long GL.

Thromb Haemost. 2000 Mar;83(3):366-70.

PMID:
10744139
15.

Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?

Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Münchau A, Klein C.

Arch Neurol. 2006 Jun;63(6):833-8.

PMID:
16769864
16.

Identification of simultaneous mutation of fibrinogen alpha chain and protein C genes in a Japanese kindred.

Watanabe K, Shibuya A, Ishii E, Kurihara M, Inoue S, Ono M, Wada Y, Wakiyama M, Zaitsu M, Iida H, Muraoka K, Kinoshita S, Hamasaki N.

Br J Haematol. 2003 Jan;120(1):101-8.

PMID:
12492584
17.

Circulating microparticles are elevated in carriers of factor V Leiden.

Enjeti AK, Lincz LF, Scorgie FE, Seldon M.

Thromb Res. 2010 Sep;126(3):250-3. doi: 10.1016/j.thromres.2009.11.019. Epub 2009 Dec 21.

PMID:
20022357
18.

Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations (gamma Ala341Thr, Bbeta Tyr326Cys and Aalpha Asp496Asn).

Hanss M, Chevreaud C, French P, Négrier C, de Mazancourt P.

Thromb Haemost. 2007 Sep;98(3):689-91. No abstract available.

PMID:
17849064
19.

Severe protein C deficiency from compound heterozygous mutations in the PROC gene in two Korean adult patients.

Kim HJ, Kim DK, Koh KC, Kim JY, Kim SH.

Thromb Res. 2008;123(2):412-7. doi: 10.1016/j.thromres.2008.04.014. Epub 2008 Jun 24. No abstract available.

PMID:
18573519
20.

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.

Scott BT, Bovill EG, Callas PW, Hasstedt SJ, Leppert MF, Valliere JE, Varvil TS, Long GL.

Thromb Haemost. 2001 Jan;85(1):82-7.

PMID:
11204593

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