132 related articles for article (PubMed ID: 7740502)
1. Prevalence of protein C deficiency in the healthy population.
Tait RC; Walker ID; Reitsma PH; Islam SI; McCall F; Poort SR; Conkie JA; Bertina RM
Thromb Haemost; 1995 Jan; 73(1):87-93. PubMed ID: 7740502
[TBL] [Abstract][Full Text] [Related]
2. [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; 127(1-2):21-7. PubMed ID: 10377836
[TBL] [Abstract][Full Text] [Related]
3. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
Piver MS
Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
[TBL] [Abstract][Full Text] [Related]
4. Protein C deficiency: identification of a novel two-base pair insertion and two point mutations in exon 7 of the protein C gene in Spanish families.
Soria JM; Fontcuberta J; Borrell M; Estivill X; Sala N
Hum Mutat; 1992; 1(5):428-31. PubMed ID: 1301954
[TBL] [Abstract][Full Text] [Related]
5. Genetic background of type I protein C deficiency in Finland.
Kuismanen K; Levo A; Vahtera E; Rasi V; Labrouche S; Freyburger G; Krusius T; Partanen J
Thromb Res; 2006; 118(5):603-9. PubMed ID: 16360797
[TBL] [Abstract][Full Text] [Related]
6. Six different point mutations in seven Danish families with symptomatic protein C deficiency.
Lind B; Schwartz M; Thorsen S
Thromb Haemost; 1995 Feb; 73(2):186-93. PubMed ID: 7792728
[TBL] [Abstract][Full Text] [Related]
7. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
Ireland H; Thompson E; Lane DA
Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
[TBL] [Abstract][Full Text] [Related]
8. Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.
Gandrille S; Vidaud M; Aiach M; Alhenc-Gelas M; Fischer AM; Gouault-Heilman M; Toulon P; Fiessinger JN; Goossens M
Hum Mutat; 1992; 1(6):491-500. PubMed ID: 1301959
[TBL] [Abstract][Full Text] [Related]
9. High incidence of thrombophilia detected in Chinese patients with venous thrombosis.
Liu HW; Kwong YL; Bourke C; Lam CK; Lie AK; Wei D; Chan LC
Thromb Haemost; 1994 Apr; 71(4):416-9. PubMed ID: 8052955
[TBL] [Abstract][Full Text] [Related]
10. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening.
Pabinger I; Brücker S; Kyrle PA; Schneider B; Korninger HC; Niessner H; Lechner K
Blood Coagul Fibrinolysis; 1992 Oct; 3(5):547-53. PubMed ID: 1450321
[TBL] [Abstract][Full Text] [Related]
11. Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing?
Labrouche S; Reboul MP; Guérin V; Vergnes C; Freyburger G
Blood Coagul Fibrinolysis; 2003 Sep; 14(6):531-8. PubMed ID: 12960605
[TBL] [Abstract][Full Text] [Related]
12. Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanism.
Gandrille S; Jude B; Alhenc-Gelas M; Millaire A; Aiach M
Thromb Haemost; 1993 Nov; 70(5):747-52. PubMed ID: 8128429
[TBL] [Abstract][Full Text] [Related]
13. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
[TBL] [Abstract][Full Text] [Related]
14. Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.
Mahmoodi BK; Brouwer JL; Veeger NJ; van der Meer J
Circulation; 2008 Oct; 118(16):1659-67. PubMed ID: 18824642
[TBL] [Abstract][Full Text] [Related]
15. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
Miyata T; Zheng YZ; Sakata T; Tsushima N; Kato H
Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
[TBL] [Abstract][Full Text] [Related]
16. Identification of one novel and three other point mutations in the protein C gene of five unrelated brazilian patients with hereditary protein C deficiency.
Singh YS; Arruda VR; Ozello MC; Machado TF; Annichino-Bizzacchi MM
Haematologica; 2000 Aug; 85(8):891-3. PubMed ID: 10942953
[No Abstract] [Full Text] [Related]
17. Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.
Doig RG; Begley CG; McGrath KM
Thromb Haemost; 1994 Aug; 72(2):203-8. PubMed ID: 7831652
[TBL] [Abstract][Full Text] [Related]
18. [Significance of hereditary thrombophilia for risk of thrombosis with oral contraceptives].
Bauersachs R; Lindhoff-Last E; Ehrly AM; Kuhl H
Zentralbl Gynakol; 1996; 118(5):262-70. PubMed ID: 8701622
[TBL] [Abstract][Full Text] [Related]
19. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
Liu L; Guo WR; He LS; Mu H; Jiang Y; Huang FQ; Li JZ
Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):115-8. PubMed ID: 12697119
[TBL] [Abstract][Full Text] [Related]
20. Beta 2-glycoprotein I deficiency and the risk of thrombosis.
Bancsi LF; van der Linden IK; Bertina RM
Thromb Haemost; 1992 Jun; 67(6):649-53. PubMed ID: 1509404
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]