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Similar articles for PubMed (Select 19141155)

1.

Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment.

Meeks SL, Abshire TC.

Haemophilia. 2008 Nov;14(6):1159-63. doi: 10.1111/j.1365-2516.2008.01832.x. Review.

PMID:
19141155
2.

Rare inherited disorders of fibrinogen.

Acharya SS, Dimichele DM.

Haemophilia. 2008 Nov;14(6):1151-8. doi: 10.1111/j.1365-2516.2008.01831.x. Review.

PMID:
19141154
3.

Diagnosis and treatment of inherited factor X deficiency.

Brown DL, Kouides PA.

Haemophilia. 2008 Nov;14(6):1176-82. doi: 10.1111/j.1365-2516.2008.01856.x.

PMID:
19141158
4.

Factor V deficiency: a concise review.

Huang JN, Koerper MA.

Haemophilia. 2008 Nov;14(6):1164-9. doi: 10.1111/j.1365-2516.2008.01785.x. Review.

PMID:
19141156
5.

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Lapecorella M, Mariani G; International Registry on Congenital Factor VII Deficiency.

Haemophilia. 2008 Nov;14(6):1170-5. doi: 10.1111/j.1365-2516.2008.01844.x. Review.

PMID:
19141157
6.

Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficiency with a novel frameshift mutation, prothrombin saitama.

Seki M, Koh K, Inoue T, Tomita Y, Kato M, Shimizu M, Morishita E, Hanada R.

Pediatr Blood Cancer. 2013 Mar;60(3):503-5. doi: 10.1002/pbc.24387. Epub 2012 Nov 14.

PMID:
23152198
7.

Congenital prothrombin deficiency.

Lancellotti S, De Cristofaro R.

Semin Thromb Hemost. 2009 Jun;35(4):367-81. doi: 10.1055/s-0029-1225759. Epub 2009 Jul 13. Review.

PMID:
19598065
8.

Congenital deficiencies and abnormalities of prothrombin.

Girolami A, Scarano L, Saggiorato G, Girolami B, Bertomoro A, Marchiori A.

Blood Coagul Fibrinolysis. 1998 Oct;9(7):557-69. Review.

PMID:
9863703
9.

A severe neonatal presentation of factor II deficiency.

Pasmant E, Dumont B, Lacapere JJ, Dautzenberg MD, Bezeaud A.

Eur J Haematol. 2011 Nov;87(5):464-6. doi: 10.1111/j.1600-0609.2011.01670.x. Epub 2011 Aug 11.

PMID:
21692854
10.

Congenital factor II deficiency: moroccan cases.

Imane S, Laalej Z, Faez S, Oukkache B.

Int J Lab Hematol. 2013 Aug;35(4):416-20. doi: 10.1111/ijlh.12033. Epub 2012 Nov 28.

PMID:
23190616
11.

Increased thrombin generation and fibrinogen level after therapeutic plasma transfusion: relation to bleeding.

Schols SE, van der Meijden PE, van Oerle R, Curvers J, Heemskerk JW, van Pampus EC.

Thromb Haemost. 2008 Jan;99(1):64-70. doi: 10.1160/TH07-07-0438.

PMID:
18217136
12.

Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg382-Cys), Dhahran (Arg271-His), and hypoprothrombinemia.

O'Marcaigh AS, Nichols WL, Hassinger NL, Mullins JD, Mallouh AA, Gilchrist GS, Owen WG.

Blood. 1996 Oct 1;88(7):2611-8.

13.

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.

Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, Chandy M, Srivastava A.

J Thromb Haemost. 2005 Jul;3(7):1446-53.

PMID:
15892853
14.

Prothrombin Shanghai: hypoprothrombinaemia caused by substitution of Gla29 by Gly.

Wang W, Fu Q, Zhou R, Wu W, Ding Q, Hu Y, Wang X, Wang H, Wang Z.

Haemophilia. 2004 Jan;10(1):94-7.

PMID:
14962227
15.

Indications for prothrombin complex concentrates in massive transfusions.

Blauhut B.

Thromb Res. 1999 Aug 15;95(4 Suppl 1):S63-9. Review.

PMID:
10499911
16.

Factor X deficiency.

Menegatti M, Peyvandi F.

Semin Thromb Hemost. 2009 Jun;35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13. Review.

PMID:
19598069
17.

Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.

Akhavan S, Mannucci PM, Lak M, Mancuso G, Mazzucconi MG, Rocino A, Jenkins PV, Perkins SJ.

Thromb Haemost. 2000 Dec;84(6):989-97.

PMID:
11154146
18.

Factor XIII deficiency.

Hsieh L, Nugent D.

Haemophilia. 2008 Nov;14(6):1190-200. doi: 10.1111/j.1365-2516.2008.01857.x. Review.

PMID:
19141159
19.

Thromboelastography in children with coagulation factor deficiencies.

Chitlur M, Warrier I, Rajpurkar M, Hollon W, Llanto L, Wiseman C, Lusher JM.

Br J Haematol. 2008 Jun;142(2):250-6. doi: 10.1111/j.1365-2141.2008.07063.x. Epub 2008 May 19.

PMID:
18492116
20.

Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias.

Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group.

J Thromb Haemost. 2004 Feb;2(2):248-56.

PMID:
14995986
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