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Journal Abstract Search

131 related items for PubMed ID: 9890294

  • 1. Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease.
    Arruda VR, Belangero WD, Ozelo MC, Oliveira GB, Pagnano RG, Volpon JB, Annichino-Bizzacchi JM.
    J Pediatr Orthop; 1999; 19(1):84-7. PubMed ID: 9890294
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  • 3. Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis.
    Kluijtmans LA, den Heijer M, Reitsma PH, Heil SG, Blom HJ, Rosendaal FR.
    Thromb Haemost; 1998 Feb; 79(2):254-8. PubMed ID: 9493571
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  • 5. Incidence of thrombophilia in patients with Gaucher disease.
    Elstein D, Renbaum P, Levy-Lahad E, Zimran A.
    Am J Med Genet; 2000 Dec 18; 95(5):429-31. PubMed ID: 11146461
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  • 8. Meta-analysis of hypercoagulability genetic polymorphisms in Perthes disease.
    Woratanarat P, Thaveeratitharm C, Woratanarat T, Angsanuntsukh C, Attia J, Thakkinstian A.
    J Orthop Res; 2014 Jan 18; 32(1):1-7. PubMed ID: 23983171
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  • 10. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause.
    Brenner B, Sarig G, Weiner Z, Younis J, Blumenfeld Z, Lanir N.
    Thromb Haemost; 1999 Jul 18; 82(1):6-9. PubMed ID: 10456445
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  • 13. Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
    Torres JD, Cardona H, Alvarez L, Cardona-Maya W, Castañeda SA, Quintero-Rivera F, Cadavid A, Bedoya G, Tobón L.
    Am J Hematol; 2006 Dec 18; 81(12):933-7. PubMed ID: 16917913
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  • 14. Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease.
    Guédon C, Le Cam-Duchez V, Lalaude O, Ménard JF, Lerebours E, Borg JY.
    Am J Gastroenterol; 2001 May 18; 96(5):1448-54. PubMed ID: 11374681
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  • 17. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ.
    Am J Hematol; 2002 Sep 18; 71(1):11-4. PubMed ID: 12221667
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  • 19. A common haplotype for the 677T thermolabile variant of the 5,10-methylenetetrahydrofolate reductase gene in thrombophilic patients and controls.
    Linnebank M, Homberger A, Nowak-Göttl U, Koch HG.
    Hum Mutat; 2002 Dec 18; 20(6):478. PubMed ID: 12442281
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