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Results: 1 to 20 of 122

1.

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
[PubMed - indexed for MEDLINE]
2.

Congenital prothrombin deficiency: an update.

Lancellotti S, Basso M, De Cristofaro R.

Semin Thromb Hemost. 2013 Sep;39(6):596-606. doi: 10.1055/s-0033-1348948. Epub 2013 Jul 12. Review.

PMID:
23852823
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP).

Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, Rappaport EF.

Blood Coagul Fibrinolysis. 1997 Sep;8(6):337-43.

PMID:
9351523
[PubMed - indexed for MEDLINE]
6.

Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patient.

Poort SR, Njo KT, Vos HL, Bertina RM.

Blood Coagul Fibrinolysis. 1998 Nov;9(8):761-4.

PMID:
9890721
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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.

PMID:
8839854
[PubMed - indexed for MEDLINE]
Free Article
10.
11.

Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.

Iwahana H, Yoshimoto K, Shigekiyo T, Shirakami A, Saito S, Itakura M.

Am J Hum Genet. 1992 Dec;51(6):1386-95.

PMID:
1334372
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Prothrombin Greenville, Arg517-->Gln, identified in an individual heterozygous for dysprothrombinemia.

Henriksen RA, Dunham CK, Miller LD, Casey JT, Menke JB, Knupp CL, Usala SJ.

Blood. 1998 Mar 15;91(6):2026-31.

PMID:
9490687
[PubMed - indexed for MEDLINE]
Free Article
13.

Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency.

Poort SR, Landolfi R, Bertina RM.

Thromb Haemost. 1997 Apr;77(4):610-5.

PMID:
9134629
[PubMed - indexed for MEDLINE]
14.

A common mutation, Arg457-->Gln, links prothrombin deficiencies in the Puerto Rican population.

Lefkowitz JB, Weller A, Nuss R, Santiago-Borrero PJ, Brown DL, Ortiz IR.

J Thromb Haemost. 2003 Nov;1(11):2381-8.

PMID:
14629473
[PubMed - indexed for MEDLINE]
15.

Prothrombin San Antonio: a single amino acid substitution at a factor Xa activation site (Arg320 to His) results in dysprothrombinemia.

Sun WY, Burkart MC, Holahan JR, Degen SJ.

Blood. 2000 Jan 15;95(2):711-4.

PMID:
10627484
[PubMed - indexed for MEDLINE]
Free Article
16.

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
[PubMed - indexed for MEDLINE]
17.

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
[PubMed - indexed for MEDLINE]
18.

Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency.

Stanchev H, Philips M, Villoutreix BO, Aksglaede L, Lethagen S, Thorsen S.

Thromb Haemost. 2006 Jan;95(1):195-8. No abstract available.

PMID:
16543981
[PubMed - indexed for MEDLINE]
19.

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
[PubMed - indexed for MEDLINE]
20.

Severe prothrombin deficiency caused by prothrombin-Edmonton (R-4Q) combined with a previously undetected deletion.

Wong AY, Hewitt J, Clarke BJ, Hudson DM, Krisinger MJ, Dower NA, MacGillivray RT.

J Thromb Haemost. 2006 Dec;4(12):2623-8. Epub 2006 Sep 26.

PMID:
17002658
[PubMed - indexed for MEDLINE]

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