Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 117

  • Showing results for a modified search because your search retrieved no results.
1.

Antithrombin III deficiency in an Indian family.

Mohanty D, Ghosh K, Garewal G, Vajpayee RK, Prakash C, Quadri MI, Das KC.

Thromb Res. 1982 Sep 15;27(6):763-5. No abstract available.

PMID:
7179213
2.

Familial functional antithrombin III deficiency.

Sørensen PJ, Dyerberg J, Stoffersen E, Jensen MK.

Scand J Haematol. 1980 Feb;24(2):105-9.

PMID:
7375809
3.

[Congenital deficiency of antithrombin III].

Finazzi G, Barbui T.

Haematologica. 1990 Mar-Apr;75 Suppl 2:6-13. Review. Italian. No abstract available.

PMID:
2201606
4.

A Swedish family with abnormal antithrombin III.

Tengborn L, Frohm B, Nilsson LE, Nilsson IM.

Scand J Haematol. 1985 May;34(5):412-6.

PMID:
4012220
5.

[Hereditary abnormalities of antithrombin III in patients with recurrent thrombophlebitis].

Bekić-Kaluza S, Rezaković D, Musa M.

Med Arh. 1986;40(1-2):51-3. Croatian. No abstract available.

PMID:
3272307
6.
7.

[Comparative studies of the antithrombin III level and plasminogen activator activity in patients with thrombophlebitis].

Tymiński W, Czestochowska E, Swiecicki P.

Pol Tyg Lek. 1985 Oct 28;40(43):1202-4. Polish. No abstract available.

PMID:
4088936
8.

Familial antithrombin III deficiency.

Winter JH, Fenech A, Ridley W, Bennett B, Cumming AM, Mackie M, Douglas AS.

Q J Med. 1982;51(204):373-95.

PMID:
7156320
9.

Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.

Michiels JJ, van der Luit L, van Vliet HH, Jochmans K, Lissens W.

Thromb Res. 1995 May 1;78(3):251-4. No abstract available.

PMID:
7631305
11.

[Diagnosis of thrombophilia - hereditary deficiency of antithrombin III].

Al'pidovskiĭ VK, Lagutina NIa, Fedulova GA, Gerasimov AA.

Probl Gematol Pereliv Krovi. 1982 Mar;27(3):51-5. Russian. No abstract available.

PMID:
6806802
12.

Purification and partial characterization of a hereditary abnormal antithrombin III fraction of a patient with recurrent thrombophlebitis.

Tran TH, Bounameaux H, Bondeli C, Honkanen H, Marbet GA, Duckert F.

Thromb Haemost. 1980 Oct 31;44(2):87-91. No abstract available.

PMID:
7455996
13.

[A family with venous thrombosis and hereditary antithrombin III deficiency].

Michiels JJ, van Vliet HD.

Ned Tijdschr Geneeskd. 1986 Jan 4;130(1):28-31. Dutch. No abstract available.

PMID:
3951576
14.

[Thrombosis patients with familial antithrombin-III deficiency treated with heparin and antithrombin].

Brandt P.

Ugeskr Laeger. 1981;143(34):2145-8. Danish. No abstract available.

PMID:
7281335
15.
16.

[Deep venous thrombosis and changes in antithrombin III in the postoperative period].

Lasierra Cirujeda L, Martínez Celada M, Aza Pascual-Salcedo MJ, Hebrero San Martín J, Fernández Villamor A, Arévalo Manrique A.

Sangre (Barc). 1985;30(1):9-14. Spanish. No abstract available.

PMID:
4002101
17.

Antithrombin III deficiency in a Chinese family.

Concannon AJ, Low J.

Med J Aust. 1981 May 16;1(10):521-3.

PMID:
7254014
18.

[Heparin cofactor II studies in thrombophilic patients].

Pál A, Sas G.

Orv Hetil. 1990 Mar 4;131(9):461-2, 465. Review. Hungarian.

PMID:
2179813
19.

[Thromboembolism. The clinical significance of antithrombin III].

Schramm W.

Internist (Berl). 1984 Feb;25(2):88-92. German. No abstract available.

PMID:
6368458
20.

A novel nonsense mutation in the antithrombin III gene (Cys-4-->stop) causing recurrent venous thrombosis.

Saleun S, De Moerloose P, Bura A, Aiach M, Emmerich J.

Blood Coagul Fibrinolysis. 1996 Jul;7(5):578-9.

PMID:
8874869

Supplemental Content

Support Center