Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update-Reference-Cited by-同舟云学术

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Published:2009-11-19 Issue:1 Volume:119 Page:1-4
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Mackenzie Ian R. A.,Neumann Manuela,Bigio Eileen H.,Cairns Nigel J.,Alafuzoff Irina,Kril Jillian,Kovacs Gabor G.,Ghetti Bernardino,Halliday Glenda,Holm Ida E.,Ince Paul G.,Kamphorst Wouter,Revesz Tamas,Rozemuller Annemieke J. M.,Kumar-Singh Samir,Akiyama Haruhiko,Baborie Atik,Spina Salvatore,Dickson Dennis W.,Trojanowski John Q.,Mann David M. A.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-009-0612-2.pdf

Reference14 articles.

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2. Holm IE, Englund E, Mackenzie IRA, Johannsen P, Isaacs A (2007) A reassessment of the neuropathology of frontotemporal dementia linked to chromosome 3 (FTD-3). J Neuropathol Exp Neurol 66:884–891. doi: 10.1097/nen.0b013e3181567f02

3. Holm IE, Isaacs A, Mackenzie IRA (2009) Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene. Acta Neuropathol 118:719–720. doi: 10.1007/s00401-009-0593-1

4. Kovacs GG, Murrell JR, Horvath S et al (2009) TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy and chorea. Mov Disord 24:1843–1847. doi: 10.1002/mds.22697

5. Kwiatkowski TJ, Bosco DA, LeClerc AL et al (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323:1205–1208. doi: 10.1126/science.1166066

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