Vanmassenhove B - Search Results

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Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.

Kühnlein P, Sperfeld AD, Vanmassenhove B, Van Deerlin V, Lee VM, Trojanowski JQ, Kretzschmar HA, Ludolph AC, Neumann M. Kühnlein P, et al. Among authors: vanmassenhove b. Arch Neurol. 2008 Sep;65(9):1185-9. doi: 10.1001/archneur.65.9.1185. Arch Neurol. 2008. PMID: 18779421 Free PMC article.

A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.

Neumann M, Mittelbronn M, Simon P, Vanmassenhove B, de Silva R, Lees A, Klapp J, Meyermann R, Kretzschmar HA. Neumann M, et al. Among authors: vanmassenhove b. Neuropathol Appl Neurobiol. 2005 Aug;31(4):362-73. doi: 10.1111/j.1365-2990.2005.00629.x. Neuropathol Appl Neurobiol. 2005. PMID: 16008820

Novel G335V mutation in the tau gene associated with early onset familial frontotemporal dementia.

Neumann M, Diekmann S, Bertsch U, Vanmassenhove B, Bogerts B, Kretzschmar HA. Neumann M, et al. Among authors: vanmassenhove b. Neurogenetics. 2005 May;6(2):91-5. doi: 10.1007/s10048-005-0210-y. Epub 2005 Mar 12. Neurogenetics. 2005. PMID: 15765246

TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions.

Neumann M, Kwong LK, Truax AC, Vanmassenhove B, Kretzschmar HA, Van Deerlin VM, Clark CM, Grossman M, Miller BL, Trojanowski JQ, Lee VM. Neumann M, et al. Among authors: vanmassenhove b. J Neuropathol Exp Neurol. 2007 Mar;66(3):177-83. doi: 10.1097/01.jnen.0000248554.45456.58. J Neuropathol Exp Neurol. 2007. PMID: 17356379

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