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Items: 1 to 20 of 112

1.

Antifactor Xa activity in thrombophilia. Studies in a family with Ar-III deficiency.

Odegård OR, Abildgaard U.

Scand J Haematol. 1977 Feb;18(2):86-90.

PMID:
841273
2.

Antithrombin III, heparin cofactor and antifactor Xa in relation to age, sex and pathological condition.

Panicucci F, Sagripanti A, Conte B, Pinori E, Vispi M, Lecchini L.

Haemostasis. 1980;9(5):297-302.

PMID:
7409613
3.

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
4.

Hereditary antithrombin III deficiency and thromboembolic disease.

Filip DJ, Eckstein JD, Veltkamp JJ.

Am J Hematol. 1976;1(3):343-9.

PMID:
826156
5.

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
6.

Abnormal antithrombin III (antithrombin III "Budapest") as a cause of a familial thrombophilia.

Sas G, Blaskó G, Bánhegyi D, Jákó J, Pálos LA.

Thromb Diath Haemorrh. 1974 Sep 30;32(1):105-15.

PMID:
4454033
7.

Platelet antithrombin deficiency: a new clinical entity.

Tullis JL, Watanabe K.

Am J Med. 1978 Sep;65(3):472-8.

PMID:
102191
8.

Hereditary antithrombin III deficiency in an English family.

Scully MF, De Haas H, Chan P, Kakkar VV.

Br J Haematol. 1981 Feb;47(2):235-40.

PMID:
7470393
9.
10.

[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
11.

Antithrombin-3 deficiency in a Dutch family.

van der Meer J, Stoepman-van Dalen EA, Jansen JM.

J Clin Pathol. 1973 Jul;26(7):532-8.

12.

Antithrombin III deficiency.

Cucuianu M, Blaga S, Pop S, Olinic D, Olinic N, Colhon D, Cristea A.

Rom J Intern Med. 1994 Apr-Jun;32(2):119-27.

PMID:
7920326
13.

Hereditary thrombophilia among 217 consecutive patients with thromboembolic disease in Jordan.

Awidi AS, Abu-Khalaf M, Herzallah U, Abu-Rajab A, Shannak MM, Abu-Obeid T, al-Taher I, Anshasi B.

Am J Hematol. 1993 Oct;44(2):95-100.

PMID:
8266926
14.

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
15.
16.

Distinction of two pathologic antithrombin III molecules: antithrombin III "Aalborg' and antithrombin III "Budapest'.

Sørensen PJ, Sas G, Petó I, Blaskó G, Kremmer T, Samu A.

Thromb Res. 1982 May 1;26(3):211-9.

PMID:
7112514
17.

AT III Barcelona: a familial quantitative-qualitative AT III deficiency.

Grau E, Fontcuberta J, Félez J, de Diego I, Soto R, Rutllant ML.

Thromb Haemost. 1988 Feb 25;59(1):13-7.

PMID:
3363529
18.

Homozygous or compound heterozygous qualitative antithrombin III deficiency.

Cucuianu M, Blaga S, Pop S, Olinic D, Olinic N, Colhon D, Cristea A.

Nouv Rev Fr Hematol. 1994 Aug;36(4):335-7.

PMID:
7971256
19.

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
20.

Antithrombin III Geneva: a hereditary abnormal AT III with defective heparin cofactor activity.

de Moerloose PA, Reber G, Vernet P, Minazio P, Bouvier CA.

Thromb Haemost. 1987 Apr 7;57(2):154-7.

PMID:
3603409

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