These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

85 related articles for article (PubMed ID: 8339996)

  • 1. 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. PubMed ID: 8339996
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 57(2):183-6. PubMed ID: 3037717
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 2467857
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary dysfunctional protein C molecules (type II): assay characterization and proposed classification.
    Marlar RA; Adcock DM; Madden RM
    Thromb Haemost; 1990 Jun; 63(3):375-9. PubMed ID: 2402741
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
    Zhou RF; Wang HL; Fu QH; Wang WB; Wu WM; Ding QL; Xie S; Hu YQ; Wang XF; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Oct; 83(19):1694-7. PubMed ID: 14642106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A sporadic case of protein C deficiency].
    Ishimaru F; Hayashi H; Ueki K; Fujita T; Tsurumi N; Tsuda T; Kimura I
    Rinsho Ketsueki; 1990 Nov; 31(11):1856-61. PubMed ID: 2287072
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 19133979
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Protein C deficiency in two Austrian families.
    Pabinger-Fasching I; Bertina RM; Lechner K; Niessner H; Korninger C
    Thromb Haemost; 1983 Dec; 50(4):810-3. PubMed ID: 6665761
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. 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. PubMed ID: 8136274
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis of protein C deficiency in patients on oral anticoagulant treatment: comparison of three different functional protein C assays.
    Pabinger I; Kyrle PA; Speiser W; Stoffels U; Jung M; Lechner K
    Thromb Haemost; 1990 Jun; 63(3):407-12. PubMed ID: 2402742
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Plasminogen deficiencies in 2 Spanish families. Response to the administration of DDAVP].
    Tabernero MD; Galende J; Tomás JF; Alberca I; Estelles A; Vicente V
    Sangre (Barc); 1990 Apr; 35(2):137-41. PubMed ID: 2363094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma: characterization of the dysfunctional protein C Padua3 (protein C(R-1L/propeptide)).
    Simioni P; Kalafatis M; Tormene D; Luni S; Zerbinati P; Barzon L; Palù G; Girolami A
    Thromb Haemost; 2001 Oct; 86(4):1017-22. PubMed ID: 11686318
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inherited antithrombin III deficiency and cerebral thrombosis in a child.
    Ambruso DR; Jacobson LJ; Hathaway WE
    Pediatrics; 1980 Jan; 65(1):125-31. PubMed ID: 7355006
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Soluble endothelial protein C receptor (sEPCR) levels and venous thromboembolism in carriers of two dysfunctional protein C variants.
    Simioni P; Morboeuf O; Tognin G; Gavasso S; Tormene D; Woodhams B; Pagnan A
    Thromb Res; 2006; 117(5):523-8. PubMed ID: 15921724
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparative effects of the human protein C activator, Protac, on the activated partial thromboplastin clotting times of plasmas, with special reference to the dog.
    Johnstone IB; Martin CA
    Can J Vet Res; 2000 Apr; 64(2):117-22. PubMed ID: 10805251
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 63(2):249-57. PubMed ID: 1771629
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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. PubMed ID: 3337902
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited heterozygous protein C deficiency and dysfunctional protein S with recurrent venous thrombotic diseases: a study of three generations of a Japanese family.
    Hashizume T; Tsushima N; Matsuo H; Ito A; Oozono K; Sakata T
    Intern Med; 1992 Oct; 31(10):1197-200. PubMed ID: 1286225
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.