BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 12503653)

  • 1. Association between factor V Leiden mutation and the hemiconvulsion, hemiplegia, and epilepsy syndrome: report of two cases.
    Scantlebury MH; David M; Carmant L
    J Child Neurol; 2002 Sep; 17(9):713-7. PubMed ID: 12503653
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Factor V Leiden mutation: an unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis.
    Thorarensen O; Ryan S; Hunter J; Younkin DP
    Ann Neurol; 1997 Sep; 42(3):372-5. PubMed ID: 9307261
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cerebrovascular disorders in children with the factor V Leiden mutation.
    Lynch JK; Nelson KB; Curry CJ; Grether JK
    J Child Neurol; 2001 Oct; 16(10):735-44. PubMed ID: 11669347
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutation.
    Yamazaki S; Ikeno K; Abe T; Tohyama J; Adachi Y
    Pediatr Neurol; 2011 Sep; 45(3):193-6. PubMed ID: 21824570
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hemiconvulsion-hemiplegia-epilepsy syndrome with 1q44 microdeletion: causal or chance association.
    Gupta R; Agarwal M; Boqqula VR; Phadke RV; Phadke SR
    Am J Med Genet A; 2014 Jan; 164A(1):186-9. PubMed ID: 24214579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hemiconvulsion-hemiplegia-epilepsy syndrome with 5q33.3q34 microdeletion: Causal or chance association.
    Xue J; Song Z; Yi Z; Yang C; Li F; Liu K; Zhang Y
    Int J Dev Neurosci; 2021 Oct; 81(6):539-543. PubMed ID: 33866597
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome.
    Kim DW; Lim BC; Kim KJ; Chae JH; Lee R; Lee SK
    Epilepsy Res; 2013 Oct; 106(3):440-5. PubMed ID: 23916143
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemiconvulsion-Hemiplegia-Epilepsy Syndrome in a Girl Presented with Complex Partial Seizures.
    Joshi A; Shrestha PS; Dangol S; Shrestha NC; Poudyal P; Shrestha A
    Kathmandu Univ Med J (KUMJ); 2017 Jul-Sept.; 15(59):256-260. PubMed ID: 30353904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.
    De Stefano V; Martinelli I; Mannucci PM; Paciaroni K; Chiusolo P; Casorelli I; Rossi E; Leone G
    N Engl J Med; 1999 Sep; 341(11):801-6. PubMed ID: 10477778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis.
    Mandel H; Brenner B; Berant M; Rosenberg N; Lanir N; Jakobs C; Fowler B; Seligsohn U
    N Engl J Med; 1996 Mar; 334(12):763-8. PubMed ID: 8592550
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hemiplegic cerebral palsy and the factor V Leiden mutation.
    Halliday JL; Reddihough D; Byron K; Ekert H; Ditchfield M
    J Med Genet; 2000 Oct; 37(10):787-9. PubMed ID: 11183183
    [No Abstract]   [Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 16p13.11 microdeletion in a patient with hemiconvulsion-hemiplegia-epilepsy syndrome: a case report.
    Miteff CI; Smith RL; Bain NL; Subramanian G; Brown JE; Kamien B
    J Child Neurol; 2015 Jan; 30(1):83-6. PubMed ID: 24453159
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fatal outcome in hemiconvulsion-hemiplegia syndrome.
    Jayakody H; Joshi C
    J Child Neurol; 2014 Mar; 29(3):406-11. PubMed ID: 23271756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis.
    Weih M; Mehraein S; Valdueza JM; Einhäupl KM; Vetter B; Kulozik AE
    Stroke; 1998 Aug; 29(8):1739-40. PubMed ID: 9707222
    [No Abstract]   [Full Text] [Related]  

  • 16. The factor V Leiden mutation which predisposes to thrombosis is not common in patients with antiphospholipid syndrome.
    Dizon-Townson D; Hutchison C; Silver R; Branch DW; Ward K
    Thromb Haemost; 1995 Oct; 74(4):1029-31. PubMed ID: 8560406
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hemiconvulsion-Hemiplegia-Epilepsy in a girl with cobalamin C deficiency.
    Myers KA; Dudley RW; Srour M
    Epileptic Disord; 2018 Dec; 20(6):545-550. PubMed ID: 30530444
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy.
    Sakakibara T; Nakagawa E; Saito Y; Sakuma H; Komaki H; Sugai K; Sasaki M; Kurahashi H; Hirose S
    Epilepsia; 2009 Sep; 50(9):2158-62. PubMed ID: 19563349
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Survival following decompressive hemicraniectomy for hemiconvulsion-hemiplegia-epilepsy syndrome: case report.
    Beier AD; Jannotta GE; Sandler ED; Abram HS; Sheth RD; Aldana PR
    J Neurosurg Pediatr; 2016 Sep; 18(3):344-9. PubMed ID: 27176609
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factor V Leiden mutation in patients with Behçet's disease.
    Oner AF; Gürgey A; Gürler A; Mesci L
    J Rheumatol; 1998 Mar; 25(3):496-8. PubMed ID: 9517770
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.