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Results: 1 to 20 of 96

1.

Heparin cofactor II deficiency.

Tollefsen DM.

Arch Pathol Lab Med. 2002 Nov;126(11):1394-400. Review.

PMID:
12421148
[PubMed - indexed for MEDLINE]
2.

Dysfibrinogenemia and thrombosis.

Hayes T.

Arch Pathol Lab Med. 2002 Nov;126(11):1387-90. Review.

PMID:
12421146
[PubMed - indexed for MEDLINE]
3.

Elevated hemostatic factor levels as potential risk factors for thrombosis.

Chandler WL, Rodgers GM, Sprouse JT, Thompson AR.

Arch Pathol Lab Med. 2002 Nov;126(11):1405-14. Review.

PMID:
12421150
[PubMed - indexed for MEDLINE]
4.

College of American Pathologists Consensus Conference XXXVI: Diagnostic Issues in Thrombophilia.

[No authors listed]

Arch Pathol Lab Med. 2002 Nov;126(11):1277-433. Review.

PMID:
12421135
[PubMed - indexed for MEDLINE]
5.

Laboratory diagnosis of antithrombin and heparin cofactor II deficiency.

Tollefsen DM.

Semin Thromb Hemost. 1990 Apr;16(2):162-8. Review.

PMID:
2191430
[PubMed - indexed for MEDLINE]
6.

Hereditary heparin cofactor II deficiency and thrombosis: report of six patients belonging to two separate kindreds.

Simioni P, Lazzaro AR, Coser E, Salmistraro G, Girolami A.

Blood Coagul Fibrinolysis. 1990 Oct;1(4-5):351-6.

PMID:
2133211
[PubMed - indexed for MEDLINE]
7.

Clinical and laboratory management of the prothrombin G20210A mutation.

McGlennen RC, Key NS.

Arch Pathol Lab Med. 2002 Nov;126(11):1319-25. Review.

PMID:
12421139
[PubMed - indexed for MEDLINE]
8.

Antithrombin deficiency: issues in laboratory diagnosis.

Kottke-Marchant K, Duncan A.

Arch Pathol Lab Med. 2002 Nov;126(11):1326-36. Review.

PMID:
12421140
[PubMed - indexed for MEDLINE]
9.

[Congenital disorders of hemostasis with thrombophilia].

Egbring R, Seitz R.

Internist (Berl). 1989 Sep;30(9):577-86. Review. German. No abstract available.

PMID:
2509393
[PubMed - indexed for MEDLINE]
10.

Hyperhomocyst(e)inemia and Thrombophilia.

Key NS, McGlennen RC.

Arch Pathol Lab Med. 2002 Nov;126(11):1367-75. Review.

PMID:
12421143
[PubMed - indexed for MEDLINE]
11.

[Heparin cofactor II and thrombophilic conditions].

Hudecek J, Hal'áková E, Ivanková J, Kubisz P.

Vnitr Lek. 1997 May;43(5):317-9. Czech.

PMID:
9601856
[PubMed - indexed for MEDLINE]
12.

Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.

Villa P, Aznar J, Vaya A, España F, Ferrando F, Mira Y, Estellés A.

Thromb Haemost. 1999 Sep;82(3):1011-4.

PMID:
10494755
[PubMed - indexed for MEDLINE]
13.

[Heparin cofactor II (HCII)].

Yoshikawa T, Hayashi T, Suzuki K.

Nihon Rinsho. 2004 Dec;62 Suppl 12:667-70. Review. Japanese. No abstract available.

PMID:
15658419
[PubMed - indexed for MEDLINE]
14.

Laboratory issues in diagnosing abnormalities of protein C, thrombomodulin, and endothelial cell protein C receptor.

Kottke-Marchant K, Comp P.

Arch Pathol Lab Med. 2002 Nov;126(11):1337-48. Review.

PMID:
12421141
[PubMed - indexed for MEDLINE]
15.

Prothrombin G20210A gene mutation, heparin cofactor II defects, primary (essential) thrombocythemia, and thrombohemorrhagic manifestations.

Frenkel EP, Bick RL.

Semin Thromb Hemost. 1999;25(4):375-86. Review.

PMID:
10548071
[PubMed - indexed for MEDLINE]
16.

[EQUALIS expert group for coagulation. Functional method for the first choice diagnostics of hereditary antithrombin deficiency].

Strandberg K.

Lakartidningen. 2011 Aug 24-30;108(34):1552. Swedish. No abstract available.

PMID:
22066163
[PubMed - indexed for MEDLINE]
17.

Heparin cofactor II deficiency in renal allograft recipients: no correlation with the development of thrombosis.

Toulon P, Moulonguet-Doleris L, Costa JM, Aiach M.

Thromb Haemost. 1991 Jan 23;65(1):20-4.

PMID:
2024235
[PubMed - indexed for MEDLINE]
18.

Heparin cofactor II in adult glomerulopathy and nephrotic syndrome.

Pech MA, Rostoker G, Soria C, Lang P, Weil B, Caen J, Lagrue G.

Am J Nephrol. 1991;11(1):74-5. No abstract available.

PMID:
2048583
[PubMed - indexed for MEDLINE]
19.

[Etiological analysis of thrombophilia].

Tsuda H, Iida H, Nakahara M, Hattori S, Tanabe S, Fujise M, Kinoshita S, Hamasaki N.

Rinsho Byori. 1997 Nov;45(11):1025-30. Review. Japanese.

PMID:
9396341
[PubMed - indexed for MEDLINE]
20.

Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima.

Kanagawa Y, Shigekiyo T, Aihara K, Akaike M, Azuma H, Matsumoto T.

Thromb Haemost. 2001 Jan;85(1):101-7.

PMID:
11204559
[PubMed - indexed for MEDLINE]

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