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 *

152 related articles for article (PubMed ID: 4995085)

  • 1. Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.
    Girolami A; Lazzarin M; Scarpa R; Brunetti A
    Blood; 1971 May; 37(5):534-41. PubMed ID: 4995085
    [No Abstract]   [Full Text] [Related]  

  • 2. Another patient with a congenital hemorrhagic disorder intermediate between factor X and factor VII deficiency.
    Girolami A; Molaro G; Lazzarin M; Brunetti A; Scarpa R
    Haematol Lat; 1970; 13(1):89-102. PubMed ID: 5311839
    [No Abstract]   [Full Text] [Related]  

  • 3. Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family.
    Girolami A; Lazzarin M; Scarpa R; Brunetti A
    Haematol Lat; 1970; 13(2):169-83. PubMed ID: 5504043
    [No Abstract]   [Full Text] [Related]  

  • 4. A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
    Girolami A; Molaro G; Lazzarin M; Scarpa R; Brunetti A
    Br J Haematol; 1970 Aug; 19(2):179-92. PubMed ID: 4989292
    [No Abstract]   [Full Text] [Related]  

  • 5. Factor X Friuli coagulation disorder. Report of a newly recognized patient and some considerations on the frequency of the disease in the Friuli area.
    Girolami A; Falomo R; De Marco L; Patrassi G
    Acta Haematol; 1976; 56(1):27-38. PubMed ID: 822673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital coagulopathy due to the presence of an abnormal factor X (Friuli factor X). A "new" hemorrhagic disease].
    Girolami A; Molaro G; Brunetti A
    Recenti Prog Med; 1970 Oct; 49(4):360-84. PubMed ID: 5537614
    [No Abstract]   [Full Text] [Related]  

  • 7. Abnormal factor X (factor X Friuli) coagulation disorder. The heterozygote population. A study of 57 subjects.
    Girolami A; Brunetti A; Bareggi G; Cella G
    Acta Haematol; 1974; 51(1):40-50. PubMed ID: 4217072
    [No Abstract]   [Full Text] [Related]  

  • 8. A family with heterozygous factor X Friuli defect outside Friuli.
    Girolami A; Lazzarin M; Procidano M; Luzzatto G
    Blut; 1983 Mar; 46(3):149-54. PubMed ID: 6824795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor X survival and therapeutic factor X levels in the abnormal factor X (factor X FRIULI) COAGULATION DISORDER.
    Girolami A; Molaro G; De Marco L
    Acta Haematol; 1974; 52(4):223-31. PubMed ID: 4217528
    [No Abstract]   [Full Text] [Related]  

  • 10. Abnormal factor X(factor X Friuli) coagulation disorder.
    Girolami A; Nicolini F; Furlani E; Bareggi G
    Acta Haematol; 1973; 49(2):114-22. PubMed ID: 4196477
    [No Abstract]   [Full Text] [Related]  

  • 11. MODIFICATIONS OF THE COAGULATION MECHANISM DURING PREGNANCY.
    PHILLIPS LL
    Mod Trends Hum Reprod Physiol; 1963; 15():190-204. PubMed ID: 14115154
    [No Abstract]   [Full Text] [Related]  

  • 12. Therapy of hereditary disorders of blood coagulation.
    Breckenridge RT; Ratnoff OD
    Mod Treat; 1968 Jan; 5(1):39-60. PubMed ID: 4870179
    [No Abstract]   [Full Text] [Related]  

  • 13. Prothrombin level and activity in the abnormal factor X (factor X Friuli) hemorrhagic disorder.
    Girolami A; Sticchi A; Brunetti A
    Thromb Diath Haemorrh; 1971; 25(1):147-56. PubMed ID: 4996074
    [No Abstract]   [Full Text] [Related]  

  • 14. Lack of PIVKA effect in the abnormal factor X (factor X Friuli) coagulation disorder.
    Girolami A; Muller AD; Hemker HC
    Haemostasis; 1972; 1(1):23-30. PubMed ID: 4668760
    [No Abstract]   [Full Text] [Related]  

  • 15. Detection of the carrier state in hereditary coagulation disorders. I.
    Veltkamp JJ; Drion EF; Loeliger EA
    Thromb Diath Haemorrh; 1968 Mar; 19(1):279-303. PubMed ID: 5652235
    [No Abstract]   [Full Text] [Related]  

  • 16. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern.
    Girolami A; Fabris F; Dal Bo Zanon R; Ghiotto G; Burul A
    J Lab Clin Med; 1978 Mar; 91(3):387-95. PubMed ID: 627745
    [No Abstract]   [Full Text] [Related]  

  • 17. Hereditary prothrombin deficiency.
    Kattlove HE; Shapiro SS; Spivack M
    N Engl J Med; 1970 Jan; 282(2):57-61. PubMed ID: 4982446
    [No Abstract]   [Full Text] [Related]  

  • 18. The factor-X defect: recognition of abnormal forms of factor X.
    Denson KW; Lurie A; De Cataldo F; Mannucci PM
    Br J Haematol; 1970 Mar; 18(3):317-27. PubMed ID: 4992553
    [No Abstract]   [Full Text] [Related]  

  • 19. [A new case of homozygous congenital factor VII deficiency. Associated factor X deficiency in some members of the family].
    Allain JP; Maillasson F; Schaeffer P; Bach C
    Ann Pediatr (Paris); 1971 Dec; 18(12):817-23. PubMed ID: 5151286
    [No Abstract]   [Full Text] [Related]  

  • 20. [Incompatible blood transfusion in obstetrics and acute coagulation disorder].
    Almuna R; Campodonico I; Peralta O
    Rev Chil Obstet Ginecol; 1971; 36(4):202-9. PubMed ID: 5317403
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.