Skip to main content

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 74.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literatur

  • Aicardi J, Chevrie JJ (1982) Atypical benign partial epilepsy of childhood, Dev Med Child Neurol 24:281–292

    PubMed  CAS  Google Scholar 

  • Aicardi J, Levy G (1992) Clinical and electroencephalographic symptomatology of the »genuine« Lennox-Gastaut syndrome and its differentiation from other forms of epilepsy of early childhood, Epilepsy Res Suppl 6:185–193

    PubMed  CAS  Google Scholar 

  • Berkovic SF, Carpenter S, Evans A et al. (1989) Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study. Brain 112: 1231–1260

    PubMed  Google Scholar 

  • Berkovic SF, Cochius J, Andermann E, Andermann F (1993) Progressive myoclonus epilepsies: clinical and genetic aspects. Epilepsia 34[Suppl 3]:S19–S30

    PubMed  Google Scholar 

  • Bhatia KP, Brown P, Gregory R et al. (1995) Progressive myoclonic ataxia associated with coeliac disease — the myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain 118:1087–1093

    PubMed  Google Scholar 

  • Blume WT (1987) Lennox-Gastaut syndrome. In: Lüders H, Lesser RP, Swash M (eds) Epilepsy: Electroclinical syndromes. Springer, New York, pp 73–92

    Google Scholar 

  • Brown P (2002) Neurophysiology of the startle syndrome and hyperekplexia. Adv Neurol 89:153–159

    PubMed  Google Scholar 

  • Brown P, Thompson PD (2001) Electrophysiological aids to the diagnosis of psychogenic jerks, spasms, and tremor. Mov Disord 16:595–599

    Article  PubMed  CAS  Google Scholar 

  • Caviness JN (2002) Epidemiology of myoclonus. Adv Neurol 89:19–22

    PubMed  Google Scholar 

  • Caviness JN, Alving LI, Maraganore DM et al. (1999) The incidence and prevalence of myoclonus in Olmsted County, Minnesota. Mayo Clin Proc 74:565–569

    Article  PubMed  CAS  Google Scholar 

  • Celesia GG, Grigg MM, Ross E (1988) Generalized status myoclonicus in acute anoxic and toxic-metabolic encephalopathies. Arch Neurol 45:781–784

    PubMed  CAS  Google Scholar 

  • Cockerell OC, Rothwell J, Thompson PD, Marsden CD, Shorvon SD (1996) Clinical and physiological features of epilepsia partialis continua. Cases ascertained in the UK. Brain 119:393–407

    PubMed  Google Scholar 

  • Commission on Classification and Terminology of the International League Against Epilepsy (1989) A revised proposal for the classification of epilepsy and epileptic syndromes. Epilepsia 30:389–399

    Google Scholar 

  • Cooper JD (2003) Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis. Curr Opin Neurol 16:121–128

    Article  PubMed  CAS  Google Scholar 

  • Deuschl G, Wilms H (2002) Palatal tremor: the clinical spectrum and physiology of a rhythmic movement disorder. Adv Neurol 89:115–130

    PubMed  Google Scholar 

  • Doose H (1992) Myoclonic-astatic epilepsy. Epilepsy Res [Suppl 6]:163–168

    Google Scholar 

  • Doose H (1992) Myoclonic-astatic epilepsy [Review]. Epilepsy Research [Suppl 6]:163–168

    Google Scholar 

  • Frucht SJ (2002) The clinical challenge of posthypoxic myoclonus. Adv Neurol 89:85–88

    PubMed  Google Scholar 

  • Frucht SJ, Louis ED, Chuang C, Fahn S (2001) A pilot tolerability and efficacy study of levetiracetam in patients with chronic myoclonus. Neurology 57:1112–1114

    PubMed  CAS  Google Scholar 

  • Fukuhara N (1991) MERRF: a clinicopathological study. Relationships between myoclonus epilepsies and mitochondrial myopathies. Rev Neurol (Paris) 147:476–469

    PubMed  CAS  Google Scholar 

  • Hallett M (2002) Neurophysiology of brainstem myoclonus. Adv Neurol 89:99–102

    PubMed  Google Scholar 

  • Krumholz A, Stern BJ, Weiss HD (1988) Outcome from coma after cardiopulmonary resuscitation: Relation to seizures and myoclonus. Neurology 38:401–405

    PubMed  CAS  Google Scholar 

  • Lance JW (1986) Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes. Adv Neurol 43:33–55

    PubMed  CAS  Google Scholar 

  • Lehesjoki AE (2002) Clinical features and genetics of Unverricht-Lundborg disease. Adv Neurol 89:193–197

    PubMed  Google Scholar 

  • Lempert T, Bauer M, Schmidt D (1994) Syncope: a videometric analysis of 56 episodes of transient cerebral hypoxia. Ann Neurol 36:233–237

    Article  PubMed  CAS  Google Scholar 

  • Marsden CD, Hallett M, Fahn S (1981) The nosology and pathophysiology of myoclonus. In: Marsden CD, Fahn S (eds) Neurology 2 — Movement disorders. Butterworth Scientific, London, pp 196–248

    Google Scholar 

  • Marsden CD, Harding AE, Obeso JA, Lu CS (1990) Progressive myoclonic ataxia (The Ramsay Hunt syndrome). Arch Neurol 47:1121–1125

    PubMed  CAS  Google Scholar 

  • Minassian BA (2002) Progressive myoclonus epilepsy with polyglucosan bodies: Lafora disease. Adv Neurol 89:199–210

    PubMed  Google Scholar 

  • Pranzatelli MR, Nadi NS (1995) Mechanism of action of antiepileptic and antimyoclonic drugs. Adv Neurol 67:329–360

    PubMed  CAS  Google Scholar 

  • Rothwell JC (2002) Pathophysiology of spinal myoclonus. Adv Neurol 89:137–144

    PubMed  Google Scholar 

  • Shiang R, Ryan SG, Zhu YZ (1993) Mutations in the alpha1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia. Nat Genet 5: 351–357

    Article  PubMed  CAS  Google Scholar 

  • Shibasaki H (2002) Physiology of negative myoclonus. Adv Neurol 89:103–113

    PubMed  Google Scholar 

  • Tassinari CA, Lyagoubi S, Santos V, Gambarelli F, Roger J, Dravet C, Gastaut H (1970) Studies on spike and wave discharges in man. II. Clinical and EEG aspects of myoclonic absences. Electroencephalogr Clin Neurophysiol 29:103

    PubMed  CAS  Google Scholar 

  • Thomas JE, Reagan TJ, Klass DW (1977) Epilepsia partialis continua. A review of 32 cases. Arch Neurol 34:266–275

    PubMed  CAS  Google Scholar 

  • Thomas PK, Abrams JD, Swallow D, Stewart G (1979) Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobilities of some enzymes known to be glycoproteins. 1. Clinical findings. J Neurol Neurosurg Psychiatry 42:873–880

    PubMed  CAS  Google Scholar 

  • Thompson PD (2002) Neurodegenerative causes of myoclonus. Adv Neurol 89:31–34

    PubMed  Google Scholar 

  • Ugawa Y, Hanajima R, Okabe S, Yuasa K (2002) Neurophysiology of cortical positive myoclonus. Adv Neurol 89:89–97

    PubMed  Google Scholar 

  • Van Cott AC, Blatt I, Brenner RP (1996) Stimulus-sensitive seizures in postanoxic coma. Epilepsia 37:868–874

    Article  PubMed  Google Scholar 

  • Werhahn KJ, Brown P, Thompson PD, Marsden CD (1997) The clinical features and prognosis of chronic post hypoxic myoclonus. Mov Disord 12:216–220

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2005 Springer Medizin Verlag Heidelberg

About this chapter

Cite this chapter

Werhahn, K.J. (2005). Myoklonien. In: Schmitz, B., Tettenborn, B. (eds) Paroxysmale Störungen in der Neurologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-26665-8_11

Download citation

  • DOI: https://doi.org/10.1007/3-540-26665-8_11

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-40789-8

  • Online ISBN: 978-3-540-26665-5

  • eBook Packages: Medicine (German Language)

Publish with us

Policies and ethics