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Results: 1 to 20 of 176

1.

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
[PubMed - indexed for MEDLINE]
2.

Antithrombin III Toyama: a hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitis.

Sakuragawa N, Takahashi K, Kondo S, Koide T.

Thromb Res. 1983 Jul 15;31(2):305-17.

PMID:
6636045
[PubMed - indexed for MEDLINE]
3.

Antithrombin III Kumamoto II; a single mutation at Arg393-His increased the affinity of antithrombin III for heparin.

Okajima K, Abe H, Wagatsuma M, Okabe H, Takatsuki K.

Am J Hematol. 1995 Jan;48(1):12-8.

PMID:
7832187
[PubMed - indexed for MEDLINE]
4.

A functional abnormal antithrombin III (AT III) deficiency: AT III Charleville.

Aiach M, Nora M, Fiessinger JN, Roncato M, François D, Gelas MA.

Thromb Res. 1985 Sep 1;39(5):559-70.

PMID:
4082101
[PubMed - indexed for MEDLINE]
5.

Immunoelectrophoretic evidence of a thrombin-induced abnormality in a new variant of hereditary dysfunctional antithrombin III (AT III 'Vicenza').

Barbui T, Finazzi G, Rodeghiero F, Dini E.

Br J Haematol. 1983 Aug;54(4):561-5.

PMID:
6871107
[PubMed - indexed for MEDLINE]
6.

Homozygous variant of antithrombin III that lacks affinity for heparin, AT III Kumamoto.

Okajima K, Ueyama H, Hashimoto Y, Sasaki Y, Matsumoto K, Okabe H, Inoue M, Araki S, Takatsuki K.

Thromb Haemost. 1989 Feb 28;61(1):20-4.

PMID:
2749590
[PubMed - indexed for MEDLINE]
7.

Antithrombin III Glasgow: a variant with increased heparin affinity and reduced ability to inactivate thrombin, associated with familial thrombosis.

Lane DA, Lowe GD, Flynn A, Thompson E, Ireland H, Erdjument H.

Br J Haematol. 1987 Aug;66(4):523-7.

PMID:
3663509
[PubMed - indexed for MEDLINE]
8.

Familial functional antithrombin III deficiency.

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

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

PMID:
7375809
[PubMed - indexed for MEDLINE]
9.

Antithrombin III "Northwick Park": a variant antithrombin with normal affinity for heparin but reduced heparin cofactor activity.

Howarth DJ, Samson D, Stirling Y, Seghatchian MJ.

Thromb Haemost. 1985 Jun 24;53(3):314-9.

PMID:
4049307
[PubMed - indexed for MEDLINE]
10.

Abnormal antithrombin III with defective serine protease binding (antithrombin III "Denver").

Sambrano JE, Jacobson LJ, Reeve EB, Manco-Johnson MJ, Hathaway WE.

J Clin Invest. 1986 Mar;77(3):887-93.

PMID:
3512602
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

[Antithrombin III deficiency and tendency to thrombosis (author's transl)].

Lechner K, Thaler E, Niessner H, Nowotny C, Partsch H.

Wien Klin Wochenschr. 1977 Apr 1;89(7):215-22. German.

PMID:
857429
[PubMed - indexed for MEDLINE]
12.

Metabolism of antithrombin III (heparin cofactor) in man: effects of venous thrombosis and of heparin administration.

Collen D, Schetz J, de Cock F, Holmer E, Verstraete M.

Eur J Clin Invest. 1977 Feb;7(1):27-35.

PMID:
65284
[PubMed - indexed for MEDLINE]
13.

Antithrombin III Alger: a new homozygous AT III variant.

Fischer AM, Cornu P, Sternberg C, Mériane F, Dautzenberg MD, Chafa O, Beguin S, Desnos M.

Thromb Haemost. 1986 Apr 30;55(2):218-21.

PMID:
3715788
[PubMed - indexed for MEDLINE]
14.

Heparin cofactor activities in a family with hereditary antithrombin III deficiency: evidence for a second heparin cofactor in human plasma.

Griffith MJ, Carraway T, White GC, Dombrose FA.

Blood. 1983 Jan;61(1):111-8.

PMID:
6184096
[PubMed - indexed for MEDLINE]
Free Article
15.

Homozygous variant of antithrombin III: AT III Fontainebleau.

Boyer C, Wolf M, Vedrenne J, Meyer D, Larrieu MJ.

Thromb Haemost. 1986 Aug 20;56(1):18-22.

PMID:
3775688
[PubMed - indexed for MEDLINE]
16.

Antithrombin III Nagasaki (Ser116-Pro): a heterozygous variant with defective heparin binding associated with thrombosis.

Okajima K, Abe H, Maeda S, Motomura M, Tsujihata M, Nagataki S, Okabe H, Takatsuki K.

Blood. 1993 Mar 1;81(5):1300-5.

PMID:
8443391
[PubMed - indexed for MEDLINE]
Free Article
17.

Familial thrombosis due to antithrombin III deficiency in a Greek family.

Stathakis NE, Papayannis AG, Antonopoulos M, Gardikas C.

Acta Haematol. 1977;57(1):47-54.

PMID:
65891
[PubMed - indexed for MEDLINE]
18.

Antithrombin Sheffield: amino acid substitution at the reactive site (Arg393 to His) causing thrombosis.

Lane DA, Erdjument H, Flynn A, Di Marzo V, Panico M, Morris HR, Greaves M, Dolan G, Preston FE.

Br J Haematol. 1989 Jan;71(1):91-6.

PMID:
2917133
[PubMed - indexed for MEDLINE]
19.

Reactivity of a hereditary abnormal antithrombin III fraction in the inhibition of thrombin and factor Xa.

Tran TH, Bondeli C, Marbet GA, Duckert F.

Thromb Haemost. 1980 Oct 31;44(2):92-5.

PMID:
7455997
[PubMed - indexed for MEDLINE]
20.

Clinical and biochemical characterization of antithrombin III Franconville, a variant with Pro 41 Leu mutation.

de Roux N, Chadeuf G, Molho-Sabatier P, Plouin PF, Aiach M.

Br J Haematol. 1990 Jun;75(2):222-7.

PMID:
2372510
[PubMed - indexed for MEDLINE]

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