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Items: 1 to 20 of 90

1.

A new hereditary abnormal protein C (protein C Yonago) with a dysfunctional Gla-domain.

Iijima K, Fukuda C, Nakamura K, Kanaoka Y, Ohgi S, Mori T.

Thromb Res. 1991 Jul 15;63(2):249-57.

PMID:
1771629
2.

Dysfunctional activated protein C (PC Cádiz) in a patient with thrombotic disease.

Sala N, Borrell M, Bauer KA, Viganò-D'Angelo S, Fontcuberta J, Félez J, Rutllant ML.

Thromb Haemost. 1987 Apr 7;57(2):183-6.

PMID:
3037717
3.

A family with an abnormal protein C and a thrombotic tendency.

Girolami A, Simioni P, Lazzaro AR, Girolami B, Prandoni P.

Haematologia (Budap). 1993;25(1):25-33.

PMID:
8339996
4.

A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++.

Girolami A, Simioni P, Girolami B, Marchiori A, Millar DS, Bignell P, Kakkar VV, Cooper DN.

Br J Haematol. 1993 Nov;85(3):521-7.

PMID:
8136274
5.
7.

Protein C Sapporo (protein C Glu 25 --> Lys): a heterozygous missense mutation in the Gla domain provides new insight into the interaction between protein C and endothelial protein C receptor.

Nakabayashi T, Mizukami K, Naitoh S, Takeda M, Shikamoto Y, Nakagawa T, Kaneko H, Tarumi T, Mizoguchi I, Mizuno H, Ieko M, Koike T.

Thromb Haemost. 2005 Nov;94(5):942-50.

PMID:
16363234
8.

The protein C omega-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity.

Preston RJ, Morse C, Murden SL, Brady SK, O'Donnell JS, Mumford AD.

Br J Haematol. 2009 Mar;144(6):946-53. doi: 10.1111/j.1365-2141.2008.07550.x. Epub 2008 Dec 26.

PMID:
19133979
9.

Familial dysfunction of protein S.

Mannucci PM, Valsecchi C, Krachmalnicoff A, Faioni EM, Tripodi A.

Thromb Haemost. 1989 Sep 29;62(2):763-6.

PMID:
2530648
10.

The report of an Italian family with heterozygous protein C deficiency.

Girolami A, Cappellato MG, Lazzaro AR, Simioni P, Boscaro M.

Folia Haematol Int Mag Klin Morphol Blutforsch. 1988;115(6):859-68.

PMID:
2467857
12.

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
13.

Dysfunctional protein C deficiency (type II). A report of 11 cases in 3 American families and review of the literature.

Berdeaux DH, Abshire TC, Marlar RA.

Am J Clin Pathol. 1993 Jun;99(6):677-86. Review.

PMID:
8322701
14.
15.

[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
16.

Protein C deficiency resulting from possible double heterozygosity and its response to danazol.

Gruppo RA, Leimer P, Francis RB, Marlar RA, Silberstein E.

Blood. 1988 Feb;71(2):370-4.

17.

Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity.

Gaussem P, Gandrille S, Duchemin J, Emmerich J, Alhenc-Gelas M, Aillaud MF, Aiach M.

Thromb Haemost. 1994 Jun;71(6):748-54.

PMID:
7974343
18.

Inherited deficiency of protein S in a Japanese family with recurrent venous thrombosis: a study of three generations.

Kamiya T, Sugihara T, Ogata K, Saito H, Suzuki K, Nishioka J, Hashimoto S, Yamagata K.

Blood. 1986 Feb;67(2):406-10.

19.
20.

Hereditary dysfunctional protein C molecules (type II): assay characterization and proposed classification.

Marlar RA, Adcock DM, Madden RM.

Thromb Haemost. 1990 Jun 28;63(3):375-9.

PMID:
2402741

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