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213 related items for PubMed ID: 21824561

  • 1. Inherited thrombophilia in childhood arterial stroke: data from Lebanon.
    Muwakkit SA, Majdalani M, Hourani R, Mahfouz RA, Otrock ZK, Bilalian C, Chan AK, Abboud M, Mikati MA.
    Pediatr Neurol; 2011 Sep; 45(3):155-8. PubMed ID: 21824561
    [Abstract] [Full Text] [Related]

  • 2. Inherited prothrombotic risk factors in children with stroke, transient ischemic attack, or migraine.
    Herak DC, Antolic MR, Krleza JL, Pavic M, Dodig S, Duranovic V, Brkic AB, Zadro R.
    Pediatrics; 2009 Apr; 123(4):e653-60. PubMed ID: 19336355
    [Abstract] [Full Text] [Related]

  • 3. Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?
    Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Radojkovic D.
    J Child Neurol; 2009 Jul; 24(7):823-7. PubMed ID: 19372095
    [Abstract] [Full Text] [Related]

  • 4. Stroke in children: inherited and acquired factors and age-related variations in the presentation of 48 paediatric patients.
    Del Balzo F, Spalice A, Ruggieri M, Greco F, Properzi E, Iannetti P.
    Acta Paediatr; 2009 Jul; 98(7):1130-6. PubMed ID: 19432826
    [Abstract] [Full Text] [Related]

  • 5. Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?
    Chatterjee T, Gupta N, Choudhry VP, Behari M, Saxena R, Ashraf MZ.
    Blood Coagul Fibrinolysis; 2013 Jun; 24(4):449-53. PubMed ID: 23337710
    [Abstract] [Full Text] [Related]

  • 6. Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke.
    Zenz W, Bodó Z, Plotho J, Streif W, Male C, Bernert G, Rauter L, Ebetsberger G, Kaltenbrunner K, Kurnik P, Lischka A, Paky F, Ploier R, Höfler G, Mannhalter C, Muntean W.
    Thromb Haemost; 1998 Nov; 80(5):763-6. PubMed ID: 9843168
    [Abstract] [Full Text] [Related]

  • 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.
    Kim RJ, Becker RC.
    Am Heart J; 2003 Dec; 146(6):948-57. PubMed ID: 14660985
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Dec; 17(4):200-2. PubMed ID: 15559724
    [Abstract] [Full Text] [Related]

  • 9. Atypical timing and presentation of periventricular haemorrhagic infarction in preterm infants: the role of thrombophilia.
    Harteman JC, Groenendaal F, van Haastert IC, Liem KD, Stroink H, Bierings MB, Huisman A, de Vries LS.
    Dev Med Child Neurol; 2012 Feb; 54(2):140-7. PubMed ID: 22098125
    [Abstract] [Full Text] [Related]

  • 10. Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children.
    Kenet G, Sadetzki S, Murad H, Martinowitz U, Rosenberg N, Gitel S, Rechavi G, Inbal A.
    Stroke; 2000 Jun; 31(6):1283-8. PubMed ID: 10835445
    [Abstract] [Full Text] [Related]

  • 11. Prothrombotic genetic risk factors in stroke: a possible different role in pediatric and adult patients.
    Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Damnjanovic T, Antonijevic N, Radojkovic D.
    Clin Appl Thromb Hemost; 2012 Nov; 18(6):658-61. PubMed ID: 22275392
    [Abstract] [Full Text] [Related]

  • 12. The role of classic risk factors and prothrombotic factor gene mutations in ischemic stroke risk development in young and middle-aged individuals.
    Supanc V, Sonicki Z, Vukasovic I, Solter VV, Zavoreo I, Kes VB.
    J Stroke Cerebrovasc Dis; 2014 Mar; 23(3):e171-6. PubMed ID: 24189452
    [Abstract] [Full Text] [Related]

  • 13. Methylenetetrahydrofolate reductase C677T polymorphism in Iraqi patients with ischemic stroke.
    Al-Allawi NA, Avo AS, Jubrael JM.
    Neurol India; 2009 Mar; 57(5):631-5. PubMed ID: 19934565
    [Abstract] [Full Text] [Related]

  • 14. A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.
    Kalpage HA, Sumathipala DS, Goonasekara HW, Dissanayake VH.
    J Stroke Cerebrovasc Dis; 2016 Jan; 25(1):102-9. PubMed ID: 26522268
    [Abstract] [Full Text] [Related]

  • 15. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
    [Abstract] [Full Text] [Related]

  • 16. Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.
    Celiker G, Can U, Verdi H, Yazici AC, Ozbek N, Atac FB.
    Clin Appl Thromb Hemost; 2009 Jun; 15(4):415-20. PubMed ID: 18387982
    [Abstract] [Full Text] [Related]

  • 17. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
    Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.
    Akush Ginekol (Sofiia); 2007 Jun; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 18. Thrombophilia in infancy: factor V Leiden and MTHFR or factor II double heterozygocity as a risk factor.
    Koren A, Levin C, Hujirat Y, El-Hasid R, Kutai M, Lanir N, Shalev S, Brenner B.
    Pediatr Hematol Oncol; 2003 Jun; 20(3):219-27. PubMed ID: 12637218
    [Abstract] [Full Text] [Related]

  • 19. [Mutations of genes associated with thromboses in ischemic stroke in patients with primary antiphospholipid syndrome].
    Kalashnikova LA, Dobrynina LA, Patrusheva NL, Kovalenko TF, Patrushev LI, Aleksandrova EN, Berkovskiĭ AL, Sergeeva EV, Nasonov EL.
    Ter Arkh; 2005 Jun; 77(10):49-53. PubMed ID: 16320685
    [Abstract] [Full Text] [Related]

  • 20. Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism.
    Kim SH, Hwang H, Chae JH, Kim KJ, Hwang YS, Lim BC.
    J Child Neurol; 2010 Aug; 25(8):1047-50. PubMed ID: 20110213
    [Abstract] [Full Text] [Related]

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