Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias

J. M. Burgunder, J. Finsterer, Z. Szolnoki, B. Fontaine, J. Baets, C. Van Broeckhoven, S. Di Donato, P. De Jonghe, T. Lynch, C. Mariotti, L. Schöls, A. Spinazzola, S. J. Tabrizi, C. Tallaksen, M. Zeviani, H. F. Harbo, T. Gasser

Research output: Chapter in Book/Report/Conference proceedingChapter

Original languageEnglish
Title of host publicationEuropean Handbook of Neurological Management
Number of pages10
ISBN (Print)9781405185349
Publication statusPublished - Sep 21 2011


  • Alzheimer's disease-common type of primary degenerative dementia
  • Amyloid angiopathies, cerebral amyloid angiopathy (CAA)-Dutch type, point mutation within amyloid precursor protein (APP) gene
  • Cerebral autosomal dominant arteriopathy-with subcortical infarcts, and leukencephalopathy
  • Channelopathies, ion channels-fluxes between intra-and extracellular spaces
  • Fronto-temporal lobar degeneration-heterogeneous group of ftld disorders
  • Genetics of hereditary dementias
  • Migraine, familial hemiplegic migraine (FHM)-inherited in autosomal dominant way
  • Molecular diagnosis of channelopathies-epilepsies, migraine, stroke and dementias
  • Muscular channelopathies-hypokalaemic periodic paralysis, an autosomal dominantly hereditary disease and episodic muscle paralysis
  • Neurological channelopathies

ASJC Scopus subject areas

  • Neuroscience(all)

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