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.


PUBMED FOR HANDHELDS

Journal Abstract Search


95 related items for PubMed ID: 2133211

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary heparin cofactor II deficiency and the risk of development of thrombosis.
    Bertina RM, van der Linden IK, Engesser L, Muller HP, Brommer EJ.
    Thromb Haemost; 1987 Apr 07; 57(2):196-200. PubMed ID: 3603411
    [Abstract] [Full Text] [Related]

  • 3. Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.
    Villa P, Aznar J, Vaya A, España F, Ferrando F, Mira Y, Estellés A.
    Thromb Haemost; 1999 Sep 07; 82(3):1011-4. PubMed ID: 10494755
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Heparin cofactor II deficiency in renal allograft recipients: no correlation with the development of thrombosis.
    Toulon P, Moulonguet-Doleris L, Costa JM, Aiach M.
    Thromb Haemost; 1991 Jan 23; 65(1):20-4. PubMed ID: 2024235
    [Abstract] [Full Text] [Related]

  • 8. Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima.
    Kanagawa Y, Shigekiyo T, Aihara K, Akaike M, Azuma H, Matsumoto T.
    Thromb Haemost; 2001 Jan 23; 85(1):101-7. PubMed ID: 11204559
    [Abstract] [Full Text] [Related]

  • 9. Combined inherited protein S and heparin co-factor II deficiency in a patient with upper limb thrombosis: a family study.
    Simioni P, Zanardi S, Prandoni P, Girolami A.
    Thromb Res; 1992 Jul 01; 67(1):23-30. PubMed ID: 1440513
    [Abstract] [Full Text] [Related]

  • 10. Methodology and clinical significance of heparin cofactor II. Probable heparin cofactor II deficiency in a patient with cerebrovascular thrombosis.
    Tran TH, Zbinden B, Lämmle B, Duckert F.
    Semin Thromb Hemost; 1985 Oct 01; 11(4):342-6. PubMed ID: 3840916
    [Abstract] [Full Text] [Related]

  • 11. [Right ventricular thrombosis due to familial heparin cofactor II deficiency].
    Nagae N, Watanabe T, Miura M, Minowa T, Hirooka S, Washio M.
    Kyobu Geka; 1990 Sep 01; 43(10):830-4. PubMed ID: 2214444
    [Abstract] [Full Text] [Related]

  • 12. [Juvenile cerebral infarction associated with heparin cofactor II abnormality. A case report].
    Hamasaki S, Motomura M, Nakane S, Nishiura Y, Kondo S.
    Rinsho Shinkeigaku; 2000 Apr 01; 40(4):402-4. PubMed ID: 10967662
    [Abstract] [Full Text] [Related]

  • 13. Laboratory determination of heparin cofactor II.
    Ezenagu LC, Brandt JT.
    Arch Pathol Lab Med; 1986 Dec 01; 110(12):1149-51. PubMed ID: 3778142
    [Abstract] [Full Text] [Related]

  • 14. [Antithrombin III deficiency and tendency to thrombosis (author's transl)].
    Lechner K, Thaler E, Niessner H, Nowotny C, Partsch H.
    Wien Klin Wochenschr; 1977 Apr 01; 89(7):215-22. PubMed ID: 857429
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Laboratory diagnosis of antithrombin and heparin cofactor II deficiency.
    Tollefsen DM.
    Semin Thromb Hemost; 1990 Apr 01; 16(2):162-8. PubMed ID: 2191430
    [Abstract] [Full Text] [Related]

  • 17. Homozygous variant of antithrombin III that lacks affinity for heparin, AT III Kumamoto.
    Okajima K, Ueyama H, Hashimoto Y, Sasaki Y, Matsumoto K, Okabe H, Inoue M, Araki S, Takatsuki K.
    Thromb Haemost; 1989 Feb 28; 61(1):20-4. PubMed ID: 2749590
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 5.