@inbook{db28fc4220514719bd77a2a32327ec8e,
title = "Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias",
keywords = "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",
author = "Burgunder, {J. M.} and J. Finsterer and Z. Szolnoki and B. Fontaine and J. Baets and {Van Broeckhoven}, C. and {Di Donato}, S. and {De Jonghe}, P. and T. Lynch and C. Mariotti and L. Sch{\"o}ls and A. Spinazzola and Tabrizi, {S. J.} and C. Tallaksen and M. Zeviani and Harbo, {H. F.} and T. Gasser",
year = "2011",
month = sep,
day = "21",
doi = "10.1002/9781444346268.ch7",
language = "English",
isbn = "9781405185349",
volume = "2",
pages = "87--96",
booktitle = "European Handbook of Neurological Management",
publisher = "Wiley-Blackwell",
}