Pediatric Neurology
Volume 33, Issue 3 , Pages 214-216 , September 2005

Pulsatile Tinnitus in a 16-Year-Old Patient

  • Yoshimi Sogawa, MD

      Affiliations

    • Division of Pediatric Neurology, Schneider Children’s Hospital, New Hyde Park, New York
    • Corresponding Author InformationCommunications should be addressed to: Dr. Sogawa; Division of Pediatric Neurology; Schneider Children’s Hospital; 269-01 76th Avenue; New Hyde Park, NY 11040.
    • ,
  • Richard Libman, MD

      Affiliations

    • Department of Neurology, Long Island Jewish Medical Center, New Hyde Park, New York
    • ,
  • Lydia Eviatar, MD

      Affiliations

    • Division of Pediatric Neurology, Schneider Children’s Hospital, New Hyde Park, New York
    • ,
  • Li Kan, MD

      Affiliations

    • Division of Pediatric Neurology, Schneider Children’s Hospital, New Hyde Park, New York

Received 26 July 2004 ,Accepted 16 March 2005.

References 

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  2. Sismanis A . Pulsatile tinnitus (A 15-year experience) . Am J Otol . 1998;19:472–477
  3. Waldvogel D , Mattle HP , Sturzenegger M , Schroth G . Pulsatile tinnitus (A review of 84 patients) . J Neurol . 1998;245:137–142
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  9. Crowther MA , Kelton JG . Congenital thrombophilic states associated with venous thrombosis (A qualitative overview and proposed classification system) . Ann Intern Med . 2003;138:128–134
  10. Salomon O , Steinberg DM . Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism (Prevalence and risk assessment) . Arterioscler Thromb Vasc Biol . 1999;19:511–518
  11. Poort SR , Michiels JJ , Reitsma PH , Bertina RM . Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorder . Thromb Haemost . 1994;72:819–824
  12. Giordano P , De Lucia D , Coppola B , Iolascon A . Homozygous prothrombin gene mutation and ischemic cerebrovascular disease (A case report) . Acta Haematol . 1999;102:101–103
  13. Zawadzki C , Gaveriaux V , Trillot N , et al.   Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease (Two cases in a French family) . Thromb Haemost . 1998;80:1027–1028
  14. De Stefano V , Martinelli I , Mannucci PM , et al.   The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation . N Engl J Med . 1999;341:801–806

PII: S0887-8994(05)00191-8

doi: 10.1016/j.pediatrneurol.2005.03.012

Pediatric Neurology
Volume 33, Issue 3 , Pages 214-216 , September 2005

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