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Items: 1 to 20 of 147

1.

Protein C deficiency as the major cause of thrombophilias in childhood.

Ohga S, Ishiguro A, Takahashi Y, Shima M, Taki M, Kaneko M, Fukushima K, Kang D, Hara T; Japan Childhood Thrombophilia Study Group..

Pediatr Int. 2013 Jun;55(3):267-71. doi: 10.1111/ped.12102. Review.

PMID:
23521084
2.

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism.

Ichiyama M, Ohga S, Ochiai M, Tanaka K, Matsunaga Y, Kusuda T, Inoue H, Ishimura M, Takimoto T, Koga Y, Hotta T, Kang D, Hara T.

Pediatr Res. 2016 Jan;79(1-1):81-6. doi: 10.1038/pr.2015.180. Epub 2015 Sep 15.

PMID:
26372516
3.

Protein C and protein S deficiency - practical diagnostic issues.

Wypasek E, Undas A.

Adv Clin Exp Med. 2013 Jul-Aug;22(4):459-67.

4.

Paediatric presentation and outcome of congenital protein C deficiency in Japan.

Ohga S, Kang D, Kinjo T, Ochiai M, Doi T, Ishimura M, Kayamori Y, Urata M, Yamamoto J, Suenobu SI, Kanegane H, Ikenoue T, Shirahata A, Hara T.

Haemophilia. 2013 May;19(3):378-84. doi: 10.1111/hae.12097. Epub 2013 Feb 4.

PMID:
23379934
5.

Laboratory diagnosis of hereditary thrombophilia.

Michiels JJ, Hamulyák K.

Semin Thromb Hemost. 1998;24(4):309-20. Review.

PMID:
9763348
6.

Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?

Chatterjee T, Gupta N, Choudhry VP, Behari M, Saxena R, Ashraf MZ.

Blood Coagul Fibrinolysis. 2013 Jun;24(4):449-53. doi: 10.1097/MBC.0b013e32835bfe21.

PMID:
23337710
7.

Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort.

Caspers M, Pavlova A, Driesen J, Harbrecht U, Klamroth R, Kadar J, Fischer R, Kemkes-Matthes B, Oldenburg J.

Thromb Haemost. 2012 Aug;108(2):247-57. doi: 10.1160/TH11-12-0875. Epub 2012 May 25.

PMID:
22627591
8.

The reduced sensitivity of the ProC Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk.

Gemmati D, Serino ML, Tognazzo S, Ongaro A, Moratelli S, Gilli G, Forini E, De Mattei M, Scapoli GL.

Blood Coagul Fibrinolysis. 2001 Dec;12(8):691-7.

PMID:
11734670
9.

Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families.

Martinelli I, Mannucci PM, De Stefano V, Taioli E, Rossi V, Crosti F, Paciaroni K, Leone G, Faioni EM.

Blood. 1998 Oct 1;92(7):2353-8.

10.

[Clinical significance of anticoagulant proteins detection in patients with thrombotic events].

Zheng CC, Wu JS, Ding KY, Li J, Hu HJ, Ding XL, Liu X, Cai XY, Zhu WB.

Zhonghua Xue Ye Xue Za Zhi. 2009 Apr;30(4):264-7. Chinese.

PMID:
19731829
11.

Thrombophilia in childhood: to test or not to test.

Heleen van Ommen C, Middeldorp S.

Semin Thromb Hemost. 2011 Oct;37(7):794-801. doi: 10.1055/s-0031-1297170. Epub 2011 Dec 20. Review.

PMID:
22187402
12.

Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing?

Labrouche S, Reboul MP, Guérin V, Vergnes C, Freyburger G.

Blood Coagul Fibrinolysis. 2003 Sep;14(6):531-8.

PMID:
12960605
13.

[Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].

Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.

Srp Arh Celok Lek. 1999 Jan-Feb;127(1-2):21-7. Serbian.

PMID:
10377836
14.

Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency.

Gladson CL, Groncy P, Griffin JH.

Arch Dermatol. 1987 Dec;123(12):1701a-1706a. Review.

PMID:
2961308
15.

Protein C and protein S deficiencies.

Aiach M, Borgel D, Gaussem P, Emmerich J, Alhenc-Gelas M, Gandrille S.

Semin Hematol. 1997 Jul;34(3):205-16. Review.

PMID:
9241706
16.

Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminans.

Dogan Y, Aygun D, Yilmaz Y, Kanra G, Secmeer G, Besbas N, Gurgey A.

Pediatr Hematol Oncol. 2003 Jan-Feb;20(1):1-5.

PMID:
12687747
17.

Protein C system defects in Indian children with thrombosis.

Gupta PK, Ahmed RP, Bhattacharyya M, Kannan M, Biswas A, Kalra V, Saxena R.

Ann Hematol. 2005 Feb;84(2):85-8. Epub 2004 Sep 23.

PMID:
15449030
18.

Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.

Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.

Blood Coagul Fibrinolysis. 2003 Feb;14(2):191-6.

PMID:
12632031
20.

[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

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