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Journal Abstract Search

159 related items for PubMed ID: 8059229

  • 1.
    ; . PubMed ID:
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  • 2.
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  • 3. Hypercoagulability and thrombosis.
    Bick RL.
    Med Clin North Am; 1994 May; 78(3):635-65. PubMed ID: 8170263
    [Abstract] [Full Text] [Related]

  • 4. Hypercoagulability and thrombosis.
    Bick RL, Ucar K.
    Hematol Oncol Clin North Am; 1992 Dec; 6(6):1421-31. PubMed ID: 1452521
    [Abstract] [Full Text] [Related]

  • 5. Syndromes of thrombosis and hypercoagulability. Congenital and acquired causes of thrombosis.
    Bick RL, Kaplan H.
    Med Clin North Am; 1998 May; 82(3):409-58. PubMed ID: 9646773
    [Abstract] [Full Text] [Related]

  • 6. [Thrombophilic states].
    Chrobák L, Dulícek P.
    Vnitr Lek; 1998 Aug; 44(8):481-6. PubMed ID: 10358455
    [Abstract] [Full Text] [Related]

  • 7. [Molecular defects of coagulation factors and of the fibrinolytic system associated with thromboembolism].
    Verstraete M, Vermylen J.
    J Mal Vasc; 1987 Aug; 12(1):3-13. PubMed ID: 3549955
    [Abstract] [Full Text] [Related]

  • 8.
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  • 9. Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects.
    Bick RL.
    Hematol Oncol Clin North Am; 2003 Feb; 17(1):9-36. PubMed ID: 12627661
    [Abstract] [Full Text] [Related]

  • 10. Haematologic disorders and cerebral venous thrombosis.
    Akhtar N, Deleu D, Kamran S.
    J Pak Med Assoc; 2006 Nov; 56(11):498-501. PubMed ID: 17183975
    [Abstract] [Full Text] [Related]

  • 11. Laboratory diagnosis of hereditary thrombophilia.
    Michiels JJ, Hamulyák K.
    Semin Thromb Hemost; 1998 Nov; 24(4):309-20. PubMed ID: 9763348
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  • 12. [Diagnosis and treatment of coagulation disorders].
    Esnaola-Rojas MM.
    Rev Neurol; 1998 Nov; 29(12):1290-300. PubMed ID: 10652759
    [Abstract] [Full Text] [Related]

  • 13. Incidence of thromboembolism in association with congenital disorders in coagulation and fibrinolysis.
    Conard J, Horellou MH, Samama M.
    Acta Chir Scand Suppl; 1988 Nov; 543():15-25. PubMed ID: 2973199
    [No Abstract] [Full Text] [Related]

  • 14. The antiphospholipid and thrombosis (APL-T) syndromes. Clinical and laboratory correlates.
    Bick RL, Ancypa D.
    Clin Lab Med; 1995 Mar; 15(1):63-84. PubMed ID: 7781279
    [Abstract] [Full Text] [Related]

  • 15. Recurrent venous thrombosis and hypercoagulable states.
    Bolan CD, Alving BM.
    Am Fam Physician; 1991 Nov; 44(5):1741-51. PubMed ID: 1835274
    [Abstract] [Full Text] [Related]

  • 16. The haemostatic balance in groups of thrombosis-prone patients. With particular reference to fibrinolysis in patients with myocardial infarction.
    Gram J.
    Dan Med Bull; 1990 Jun; 37(3):210-34. PubMed ID: 2192835
    [Abstract] [Full Text] [Related]

  • 17. A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency.
    Zöller B, García de Frutos P, Dahlbäck B.
    Thromb Haemost; 1998 Apr; 79(4):802-7. PubMed ID: 9569196
    [Abstract] [Full Text] [Related]

  • 18. [Natural anticoagulants as a cause of hereditary familial thrombosis].
    Tripodi A, Mannucci PM.
    Haematologica; 1990 Apr; 75 Suppl 2():1-5. PubMed ID: 2143743
    [No Abstract] [Full Text] [Related]

  • 19.
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  • 20. Antiphospholipid and thrombosis syndromes.
    Bick RL, Baker WF.
    Semin Thromb Hemost; 1994 Apr; 20(1):3-15. PubMed ID: 8059232
    [Abstract] [Full Text] [Related]

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