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Literature DB >> 15592740

Homozygosity for factor V Leiden mutation and ischemic stroke: two case-reports and review of the literature.

Achim Allroggen, Ralf Dittrich, Martin Ritter, Rainer Dziewas, Ralf Junker, Darius G Nabavi.

Abstract

Entities: Disease Gene

Mesh：

Substances：
Factor V

Year: 2004 PMID： 15592740 DOI： 10.1007/s00415-004-0542-9

Source DB: PubMed Journal: J Neurol ISSN： 0340-5354 Impact factor: 4.849

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14 in total

1. Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.

Authors: U Nowak-Göttl; R Sträter; A Heinecke; R Junker; H G Koch; G Schuierer; A von Eckardstein
Journal: Blood Date: 1999-12-01 Impact factor: 22.113

2. Factor V Leiden and thrombophilia.

Authors: P Hopmeier; W Krugluger
Journal: N Engl J Med Date: 1995-05-18 Impact factor: 91.245

3. Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance.

Authors: J Emmerich; O Poirier; A Evans; P Marques-Vidal; D Arveiler; G Luc; M Aiach; F Cambien
Journal: Lancet Date: 1995-02-04 Impact factor: 79.321

4. Mutation in the factor V gene and the risk of myocardial infarction.

Authors: J Heinrich; T Budde; G Assmann
Journal: N Engl J Med Date: 1995-09-28 Impact factor: 91.245

5. Myocardial infarction associated with homozygous resistance to activated protein C.

Authors: J Holm; B Zöller; P J Svensson; E Berntorp; L Erhardt; B Dahlbäck
Journal: Lancet Date: 1994-10-01 Impact factor: 79.321

6. [Hereditary thrombophilia with ischemiC stroke and sinus thrombosis. Diagnosis, therapy and meta-analysis].

Authors: M Weih; J Junge-Hülsing; S Mehraein; S Ziemer; K M Einhäupl
Journal: Nervenarzt Date: 2000-12 Impact factor: 1.214

Review 7. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.

Authors: Robert J Kim; Richard C Becker
Journal: Am Heart J Date: 2003-12 Impact factor: 4.749

Homozygosity for factor V Leiden mutation and ischemic stroke: two case-reports and review of the literature.

1. Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.

2. Factor V Leiden and thrombophilia.

3. Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance.

4. Mutation in the factor V gene and the risk of myocardial infarction.

5. Myocardial infarction associated with homozygous resistance to activated protein C.

6. [Hereditary thrombophilia with ischemiC stroke and sinus thrombosis. Diagnosis, therapy and meta-analysis].

Review 7. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.

8. Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke.

9. C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study.

10. Inherited hypercoagulable states in children.

1. Evolving methods for single nucleotide polymorphism detection: Factor V Leiden mutation detection.