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

doi:10.1002/9781444346268.ch7

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

Fondazione IRCCS Istituto Neurologico "C. Besta"

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Original language	English
Title of host publication	European Handbook of Neurological Management
Publisher	Wiley-Blackwell
Pages	87-96
Number of pages	10
Volume	2
ISBN (Print)	9781405185349
DOIs	https://doi.org/10.1002/9781444346268.ch7
Publication status	Published - Sep 21 2011

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

ASJC Scopus subject areas

Neuroscience(all)

Cite this

Burgunder, J. M., Finsterer, J., Szolnoki, Z., Fontaine, B., Baets, J., Van Broeckhoven, C., ... Gasser, T. (2011). Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias. In European Handbook of Neurological Management (Vol. 2, pp. 87-96). Wiley-Blackwell. https://doi.org/10.1002/9781444346268.ch7

Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias. / Burgunder, J. M.; Finsterer, J.; Szolnoki, Z.; Fontaine, B.; Baets, J.; Van Broeckhoven, C.; Di Donato, S.; De Jonghe, P.; Lynch, T.; Mariotti, C.; Schöls, L.; Spinazzola, A.; Tabrizi, S. J.; Tallaksen, C.; Zeviani, M.; Harbo, H. F.; Gasser, T.

European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. p. 87-96.

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Burgunder, JM, Finsterer, J, Szolnoki, Z, Fontaine, B, Baets, J, Van Broeckhoven, C, Di Donato, S, De Jonghe, P, Lynch, T, Mariotti, C, Schöls, L, Spinazzola, A, Tabrizi, SJ, Tallaksen, C, Zeviani, M, Harbo, HF & Gasser, T 2011, Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias. in European Handbook of Neurological Management. vol. 2, Wiley-Blackwell, pp. 87-96. https://doi.org/10.1002/9781444346268.ch7

Burgunder, J. M. ; Finsterer, J. ; Szolnoki, Z. ; Fontaine, B. ; Baets, J. ; Van Broeckhoven, C. ; Di Donato, S. ; De Jonghe, P. ; Lynch, T. ; Mariotti, C. ; Schöls, L. ; Spinazzola, A. ; Tabrizi, S. J. ; Tallaksen, C. ; Zeviani, M. ; Harbo, H. F. ; Gasser, T. / Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias. European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. pp. 87-96

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AU - Baets, J.

AU - Van Broeckhoven, C.

AU - Di Donato, S.

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Access to Document

10.1002/9781444346268.ch7