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Journal Abstract Search

138 related items for PubMed ID: 16461766

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  • 23. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.
    El-Karaksy H, El-Koofy N, El-Hawary M, Mostafa A, Aziz M, El-Shabrawi M, Mohsen NA, Kotb M, El-Raziky M, El-Sonoon MA, A-Kader H.
    Ann Hematol; 2004 Nov; 83(11):712-5. PubMed ID: 15309526
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  • 24. Genotyping analysis of protein S-Tokushima (K196E) and the involvement of protein S antigen and activity in patients with recurrent pregnancy loss.
    Matsukawa Y, Asano E, Tsuda T, Kuma H, Kitaori T, Katano K, Ozaki Y, Sugiura-Ogasawara M.
    Eur J Obstet Gynecol Reprod Biol; 2017 Apr; 211():90-97. PubMed ID: 28214760
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  • 25. Protein S Tokushima: an abnormal protein S found in a Japanese family with thrombosis.
    Shigekiyo T, Uno Y, Kawauchi S, Saito S, Hondo H, Nishioka J, Hayashi T, Suzuki K.
    Thromb Haemost; 1993 Aug 02; 70(2):244-6. PubMed ID: 8236127
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  • 27. Clinical features in 36 patients homozygous for the ARG 506-->GLN factor V mutation.
    Emmerich J, Alhenc-Gelas M, Aillaud MF, Juhan-Vague I, Jude B, Garcin JM, Dreyfus M, de Moerloose P, Le Querrec A, Priollet P, Berruyer M, Vallantin X, Wolf M, Aiach M, Fiessinger JN.
    Thromb Haemost; 1997 Apr 02; 77(4):620-3. PubMed ID: 9134631
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  • 30. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA.
    Andersen BD, Lind B, Philips M, Hansen AB, Ingerslev J, Thorsen S.
    Thromb Haemost; 1996 Aug 02; 76(2):143-50. PubMed ID: 8865520
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  • 32. Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
    Unal S, Balta G, Duru F, Gumruk F, Altay C, Gurgey A.
    Blood Coagul Fibrinolysis; 2004 Jun 02; 15(4):343-6. PubMed ID: 15166921
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  • 33. Arg 304 Gln (FVII Padua) and Ala 294 Val mutations are equally present in patients with FVII deficiency and thrombosis.
    Girolami A, Candeo N, Bonamigo E, Fabris F.
    Eur J Haematol; 2011 Jul 02; 87(1):92-4. PubMed ID: 21453389
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  • 34. Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
    Balta G, Gürgey A.
    Turk J Pediatr; 1999 Jul 02; 41(2):197-9. PubMed ID: 10770658
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  • 37. Genetic risk factors for superficial vein thrombosis.
    Martinelli I, Cattaneo M, Taioli E, De Stefano V, Chiusolo P, Mannucci PM.
    Thromb Haemost; 1999 Oct 02; 82(4):1215-7. PubMed ID: 10544900
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  • 39. Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors.
    Espinosa-Parrilla Y, Navarro G, Morell M, Abella E, Estivill X, Sala N.
    Thromb Haemost; 2000 Jan 02; 83(1):102-6. PubMed ID: 10669162
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