Literaturverzeichnis Hyperekplexie

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  • Andermann F, et al.:
    Startle disease, or hyperekplexia
    Ann.Neurol. 1984 Sept; 16 (3): 367-8
  • Andermann F, et al.:
    Startle disorders of man: hyperekplexia, jumping and startle epilepsy.
    Brain Dev. 1988; 10 (4): 213-22
  • Dietz B. et al.:
    Hyperekplexie bei einem drei Tage alten Neugeborenen
    23. Jahrestagung der Gesellschaft für Neuropädiatrie in München ( 1997)
  • Dooley JM, et al:
    Startle disorders or hyperekplexia: adolescent onset and response to valproate.
    Pediatr Neurol. 1989 Mar-Apr; 5 (2): 126-7
  • Gastaut H.; Villeneuve A.:
    The startle disease or hyperekplexia: pathological surprise reaction.
    J. Neurol. Sci. 1967; 5: 523-542.
  • Kirstein L.; Silfverskiold B.P.:
    A family with emotionally precipitated "drop seizures."
    Acta Psychiatr Neur Scand 1958; 33: 471-476
  • Kok O.; Bruyn G.W.:
    An unidentified herditary disease. (Letter)
    Lancet I: 1359, 1962
  • Lingam S.; Wilson J.; Hart EW.:
    Hereditary stiff-baby syndrome.
    Am J Dis Child 1981; 135: 909-911.
  • Morley DJ.; Weaver DD.; Garg BP.; Markand ON.:
    Hyperexplexia: an inherited disorder of the startle response.
    Clin. Genet. 21:388- 396.
  • Ryan S.G.; Sherman S, et al.:
    Startle disease, or hyperekplexia: response clonazepam and assignement
    of the gene (STHE) to chromosome 5q by linkage analysis.
    Ann. Neurol. 31:663-668, 1992
  • Saenz-Lope E,; Herranz-Tanarro F.J.; Masden J.C.; ChaconPena J.R.:
    Hyperekplexia: a syndrome of pathological startle responses..
    Ann. Neurol. 15: 36-41. 1984
  • Sander J E.; Layzer RB.; Goldsobel AB.:
    Congenital stiff- man- syndrome.
    Ann. Neurol. 1980; 8: 195-197.
  • Shiang R.; Ryan SG.;Zhu Y.et. al.:
    Mutations in the a1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia.
    Nat. Genet. 1993; 5: 351-357.
  • Stevens H.:
    "Jumping Frenchmen of Maine"
    Arch. Neurol. 12: 311-314,1965
  • Suhren O.; Bruyn G.W.; Tuynman J.A.:
    Hyperexplexia, a hereditary startle syndrome.
    J.Neurol. Sci. 3 (1966) 577-605
  • Tijssen M.A., et al.:
    The effects of clonazepam and vigabatrin in hyperekplexia..
    J.Neurol. Sci. 149 (1997) 63-67
  • Tijssen M.A., et al.:
    Startle responses in hereditary hyperekplexia...
    Arch. Neurol.. 1997 Apr; 54 (4): 388-93