Literature DB >> 8813095

Factor V Q 506 mutation in children with thrombosis.

A Gurgey1, L Mesci, Y Renda, L Olcay, N Kocak, G Erdem.   

Abstract

The factor V Leiden mutation in 12-children with thrombosis and in 20 controls was investigated. Five heterozygous individuals and 1 homozygous individual among the cases with thrombosis and 1 heterozygous individual among controls were found. Central nervous system thromboses were increased in children with the factor V mutation, associated with protein S deficiency.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8813095     DOI: 10.1002/(SICI)1096-8652(199609)53:1<37::AID-AJH8>3.0.CO;2-6

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  2 in total

1.  Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.

Authors:  H S Kalkanoğlu; T Coşkun; S D Aydoğdu; A Tokatli; A Gürgey
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

2.  Thrombomodulin levels in Behçet's disease with and without the factor V Leiden mutation.

Authors:  A Gürgey; A Gurler; A F Oner; L Mesci; S Kirazli
Journal:  Clin Rheumatol       Date:  1998       Impact factor: 2.980

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.