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Results: 17

Related Articles by Review for PubMed (Select 9683579)

1.

An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.

Hasstedt SJ, Bovill EG, Callas PW, Long GL.

Am J Hum Genet. 1998 Aug;63(2):569-76.

2.

Protein C deficiency and venous thrombosis--the search for the second genetic defect.

Bertina RM.

Thromb Haemost. 2000 Mar;83(3):360-1. Review. No abstract available.

PMID:
10744137
3.

Protein C deficiency in a family with thromboembolism and identified gene mutations.

Hoshi S, Hijikata M, Togashi Y, Aoyagi T, Kono C, Yamada Y, Amano H, Keicho N, Yamaguchi T.

Intern Med. 2007;46(13):997-1003. Epub 2007 Jul 2. Review.

4.

Genetic risk factors of venous thrombosis.

Franco RF, Reitsma PH.

Hum Genet. 2001 Oct;109(4):369-84. Review.

PMID:
11702218
5.

[Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].

Tóth O, Dávid M, Habon T, Nagy A, Keszthelyi Z, Kovács N, Losonczy H.

Orv Hetil. 2005 Oct 9;146(41):2121-5. Review. Hungarian.

PMID:
16304806
6.

[Cerebral venous thrombosis and hereditary protein C deficiency].

Massons J, Arboix A, Oliveres M, Besses C, Muñoz C, Titus F.

Neurologia. 1992 Jan;7(1):34-8. Review. Spanish.

PMID:
1596402
7.

[Protein C deficiency and vascular thromboses. Apropos of 2 cases and a review of the literature].

Debrueres-Gris S, Lekieffre J, Werquin S, Kacet S, Jude B.

Arch Mal Coeur Vaiss. 1989 Jul-Aug;82(8):1459-65. Review. French.

PMID:
2508600
8.

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
9.

Asymptomatic homozygous protein C deficiency.

Tripodi A, Franchi F, Krachmalnicoff A, Mannucci PM.

Acta Haematol. 1990;83(3):152-5. Review.

PMID:
2109456
10.

Protein C deficiency: from gene defects to disease.

Reitsma PH.

Thromb Haemost. 1997 Jul;78(1):344-50. Review.

PMID:
9198177
11.

Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.

Alhenc-Gelas M, Emmerich J, Gandrille S, Aubry ML, Benaily N, Fiessinger JN, Aiach M.

Blood Coagul Fibrinolysis. 1995 Feb;6(1):35-41. Review.

PMID:
7795152
12.

Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months.

Tuddenham EG, Takase T, Thomas AE, Awidi AS, Madanat FF, Abu Hajir MM, Kernoff PB, Hoffbrand AV.

Thromb Res. 1989 Mar 1;53(5):475-84. Review.

PMID:
2660320
13.

[Basis of molecular cell biology on thrombosis: in the cases of protein C deficiency and protein S deficiency].

Kojima T, Katsumi A, Yamazaki K.

Rinsho Ketsueki. 1998 Feb;39(2):119-20. Review. Japanese. No abstract available.

PMID:
9545817
14.

Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Reitsma PH, Poort SR, Bernardi F, Gandrille S, Long GL, Sala N, Cooper DN.

Thromb Haemost. 1993 Jan 11;69(1):77-84. Review. No abstract available.

PMID:
8446940
15.

Mutations in protein C: molecular pathology of thrombosis.

Furie B.

J Lab Clin Med. 1992 Jun;119(6):592-3. Review. No abstract available.

PMID:
1593207
16.

[Congenital deficiency and molecular abnormality of protein C].

Eguchi Y, Matsuda M.

Rinsho Byori. 1987 May;35(5):511-3. Review. Japanese. No abstract available.

PMID:
3302411
17.

[Protein C deficiency].

Negoro N, Yoshikawa J.

Ryoikibetsu Shokogun Shirizu. 1996;(15):483-6. Review. Japanese. No abstract available.

PMID:
9048075
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