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Results: 1 to 20 of 133

1.

Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).

Celinska-Lowenhoff M, Iwaniec T, Alhenc-Gelas M, Musial J, Undas A.

Thromb Haemost. 2011 Aug;106(2):379-81. doi: 10.1160/TH11-02-0066. Epub 2011 Jun 9. No abstract available.

PMID:
21655678
[PubMed - indexed for MEDLINE]
2.

Successful outcome in a pregnant woman with homozygous antithrombin deficiency.

Alguel G, Jochmans K, Simanek R, Ay C, Quehenberger P, Langer M, Pabinger I.

Thromb Haemost. 2007 Dec;98(6):1377-8. No abstract available.

PMID:
18064341
[PubMed - indexed for MEDLINE]
3.

Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.

de la Morena-Barrio ME, Antón AI, Martínez-Martínez I, Padilla J, Miñano A, Navarro-Fernández J, Águila S, López MF, Fontcuberta J, Vicente V, Corral J.

Thromb Haemost. 2012 Mar;107(3):430-7. doi: 10.1160/TH11-10-0701. Epub 2012 Jan 11.

PMID:
22234719
[PubMed - indexed for MEDLINE]
4.

Influence of natural SERPINC1 mutations on ex vivo thrombin generation.

Alhenc-Gelas M, Canonico M, Picard V.

J Thromb Haemost. 2010 Apr;8(4):845-8. doi: 10.1111/j.1538-7836.2010.03750.x. Epub 2010 Jan 17. No abstract available.

PMID:
20088933
[PubMed - indexed for MEDLINE]
5.

[Hereditary antithrombin deficiency resulting in severe neonatal thrombosis].

Niklassen US, Ingerslev J, Birkebaek NH.

Ugeskr Laeger. 2000 Nov 6;162(45):6081-2. Danish.

PMID:
11107947
[PubMed - indexed for MEDLINE]
6.

[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
[PubMed - indexed for MEDLINE]
7.

Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency.

Luxembourg B, Pavlova A, Geisen C, Spannagl M, Bergmann F, Krause M, Alesci S, Seifried E, Lindhoff-Last E.

Thromb Haemost. 2014 Feb;111(2):249-57. doi: 10.1160/TH13-05-0402. Epub 2013 Nov 7.

PMID:
24196373
[PubMed - indexed for MEDLINE]
8.

Antithrombin Rybnik: a new point mutation (nt 683 G>T) associated with type I antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosis.

Szymańska M, Alhenc-Gelas M, Undas A.

Blood Coagul Fibrinolysis. 2013 Jul;24(5):579-80. doi: 10.1097/MBC.0b013e32835ef7b3. No abstract available.

PMID:
23807486
[PubMed - indexed for MEDLINE]
9.

Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.

Rossi E, Chiusolo P, Za T, Marietti S, Ciminello A, Leone G, De Stefano V.

Thromb Haemost. 2007 Sep;98(3):695-7. No abstract available. Erratum in: Thromb Haemost. 2007 Oct;98(4):915.

PMID:
17849067
[PubMed - indexed for MEDLINE]
10.

Mutations in the shutter region of antithrombin result in formation of disulfide-linked dimers and severe venous thrombosis.

Corral J, Huntington JA, González-Conejero R, Mushunje A, Navarro M, Marco P, Vicente V, Carrell RW.

J Thromb Haemost. 2004 Jun;2(6):931-9.

PMID:
15140129
[PubMed - indexed for MEDLINE]
11.

Homozygous deficiency of heparin cofactor II: relevance of P17 glutamate residue in serpins, relationship with conformational diseases, and role in thrombosis.

Corral J, Aznar J, Gonzalez-Conejero R, Villa P, Miñano A, Vayá A, Carrell RW, Huntington JA, Vicente V.

Circulation. 2004 Sep 7;110(10):1303-7. Epub 2004 Aug 30.

PMID:
15337701
[PubMed - indexed for MEDLINE]
Free Article
12.

Antithrombin deficiency in Brazilian patients with venous thrombosis: molecular characterization of a single splice site mutation, an insertion and a de novo point mutation.

Arnaldi LA, Pretti FA, Zampieri JP, Ramos CF, Arruda VR, Annichino-Bizzacchi JM.

Thromb Res. 2001 Dec 15;104(6):397-403.

PMID:
11755949
[PubMed - indexed for MEDLINE]
13.

Portal vein thrombosis after aortic valve replacement surgery in a patient with antithrombin III deficiency--case presentation.

Wang YQ, Chen QL, Zhu D, Dong L.

J Cardiothorac Surg. 2014 Apr 28;9(1):73. doi: 10.1186/1749-8090-9-73.

PMID:
24775062
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

[Hereditary antithrombin deficiency and pregnancy--what is the effective thromboprophylaxis?].

Majak P, Vikskjold F, Abildgaard U.

Tidsskr Nor Laegeforen. 2003 Jan 23;123(2):144-6. Norwegian. No abstract available.

PMID:
12607492
[PubMed - indexed for MEDLINE]
Free Article
15.

Intracranial venous thrombosis associated with severe antithrombin-III deficiency in pregnancy.

Ozsener S, Terek MC, Saydam G, Celebisoy N, Oztekin K, Ozkinay E.

J Obstet Gynaecol Res. 2001 Apr;27(2):81-4.

PMID:
11396643
[PubMed - indexed for MEDLINE]
16.

Deficiencies of natural anticoagulants, protein C, protein S, and antithrombin.

Lipe B, Ornstein DL.

Circulation. 2011 Oct 4;124(14):e365-8. doi: 10.1161/CIRCULATIONAHA.111.044412. No abstract available.

PMID:
21969320
[PubMed - indexed for MEDLINE]
Free Article
17.

Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family.

Gemmati D, Serino ML, Moratelli S, Mari R, Ballerini G, Scapoli GL.

Blood Coagul Fibrinolysis. 1998 Mar;9(2):173-6.

PMID:
9622215
[PubMed - indexed for MEDLINE]
18.

[Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].

Tóth O, Dávid M, Habon T, Nagy A, Keszthelyi Z, Kovács N, Losonczy H.

Orv Hetil. 2005 Oct 9;146(41):2121-5. Review. Hungarian.

PMID:
16304806
[PubMed - indexed for MEDLINE]
19.

Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiency.

Fitches AC, Lewandowski K, Olds RJ.

Thromb Haemost. 2001 Oct;86(4):1023-7.

PMID:
11686319
[PubMed - indexed for MEDLINE]
20.

Five novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis.

Nagaizumi K, Inaba H, Amano K, Suzuki M, Arai M, Fukutake K.

Int J Hematol. 2003 Jul;78(1):79-83.

PMID:
12894857
[PubMed - indexed for MEDLINE]

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