Skip to main content
Top
Published in: Journal of Neurology 6/2013

01-06-2013 | Letter to the Editors

Generalized myoclonus as a prominent symptom in a patient with FTLD-TDP

Authors: Martin Pail, Radoslav Matej, Ivica Husarova, Irena Rektorova

Published in: Journal of Neurology | Issue 6/2013

Login to get access

Excerpt

Dear Sirs, …
Appendix
Available only for authorised users
Literature
1.
go back to reference Fahn S, Marsden CD, Van Woert MH (1986) Definition and classification of myoclonus. Adv Neurol 43:1–5PubMed Fahn S, Marsden CD, Van Woert MH (1986) Definition and classification of myoclonus. Adv Neurol 43:1–5PubMed
2.
go back to reference Caviness JN (2003) Myoclonus and neurodegenerative disease—what’s in a name? Parkinsonism Relat Disord 9:185–192PubMedCrossRef Caviness JN (2003) Myoclonus and neurodegenerative disease—what’s in a name? Parkinsonism Relat Disord 9:185–192PubMedCrossRef
3.
go back to reference Zerr I, Kallenberg K, Summers DM et al (2009) Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain 132:2659–2668PubMedCrossRef Zerr I, Kallenberg K, Summers DM et al (2009) Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain 132:2659–2668PubMedCrossRef
4.
go back to reference Mackenzie IR, Neumann M, Baborie A, Sampathu DM, Du Plessis D, Jaros E, Perry RH, Trojanowski JQ, Mann DM, Lee VM (2011) A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol 122:111–113PubMedCrossRef Mackenzie IR, Neumann M, Baborie A, Sampathu DM, Du Plessis D, Jaros E, Perry RH, Trojanowski JQ, Mann DM, Lee VM (2011) A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol 122:111–113PubMedCrossRef
5.
go back to reference Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD (2011) Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration. Brain 134:2565–2581PubMedCrossRef Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD (2011) Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration. Brain 134:2565–2581PubMedCrossRef
6.
go back to reference Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Trojanowski JQ, Lee VM (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133PubMedCrossRef Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Trojanowski JQ, Lee VM (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133PubMedCrossRef
7.
go back to reference Rascovsky K, Hodges JR, Knopman D et al (2011) Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 134:2456–2477PubMedCrossRef Rascovsky K, Hodges JR, Knopman D et al (2011) Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 134:2456–2477PubMedCrossRef
8.
go back to reference Sorbi S, Hort J, Erkinjuntti T et al (2012) EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia. Eur J Neurol 19:1159–1179PubMedCrossRef Sorbi S, Hort J, Erkinjuntti T et al (2012) EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia. Eur J Neurol 19:1159–1179PubMedCrossRef
9.
go back to reference Masellis M, Momeni P, Meschino W, Heffner R, Elder J, Sato C, Liang Y, George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E (2006) Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome. Brain 29:3115–3123CrossRef Masellis M, Momeni P, Meschino W, Heffner R, Elder J, Sato C, Liang Y, George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E (2006) Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome. Brain 29:3115–3123CrossRef
10.
go back to reference Civardi C, Collini A, Mazzini L, Testa L, Monaco F (2010) Isolated continuous lingual myoclonus: unusual presentation of amyotrophic lateral sclerosis. Mov Disord 25:1309–1310PubMedCrossRef Civardi C, Collini A, Mazzini L, Testa L, Monaco F (2010) Isolated continuous lingual myoclonus: unusual presentation of amyotrophic lateral sclerosis. Mov Disord 25:1309–1310PubMedCrossRef
Metadata
Title
Generalized myoclonus as a prominent symptom in a patient with FTLD-TDP
Authors
Martin Pail
Radoslav Matej
Ivica Husarova
Irena Rektorova
Publication date
01-06-2013
Publisher
Springer-Verlag
Published in
Journal of Neurology / Issue 6/2013
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-013-6942-y

Other articles of this Issue 6/2013

Journal of Neurology 6/2013 Go to the issue