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779 results

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Page 1
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.
Pirici D, Vandenberghe R, Rademakers R, Dermaut B, Cruts M, Vennekens K, Cuijt I, Lübke U, Ceuterick C, Martin JJ, Van Broeckhoven C, Kumar-Singh S. Pirici D, et al. Among authors: van broeckhoven c. J Neuropathol Exp Neurol. 2006 Mar;65(3):289-301. doi: 10.1097/01.jnen.0000205147.39210.c7. J Neuropathol Exp Neurol. 2006. PMID: 16651890
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression.
Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M. Theuns J, et al. Among authors: van duijn cm, van broeckhoven cv, van den broeck mv. Hum Mol Genet. 2000 Feb 12;9(3):325-31. doi: 10.1093/hmg/9.3.325. Hum Mol Genet. 2000. PMID: 10655540 Free article.
The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample.
Dermaut B, Theuns J, Sleegers K, Hasegawa H, Van den Broeck M, Vennekens K, Corsmit E, St George-Hyslop P, Cruts M, van Duijn CM, Van Broeckhoven C. Dermaut B, et al. Among authors: van duijn cm, van den broeck m, van broeckhoven c. Am J Hum Genet. 2002 Jun;70(6):1568-74. doi: 10.1086/340732. Epub 2002 Apr 24. Am J Hum Genet. 2002. PMID: 11992262 Free PMC article.
Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric.
Kumar-Singh S, Cras P, Wang R, Kros JM, van Swieten J, Lübke U, Ceuterick C, Serneels S, Vennekens K, Timmermans JP, Van Marck E, Martin JJ, van Duijn CM, Van Broeckhoven C. Kumar-Singh S, et al. Among authors: van swieten j, van duijn cm, van marck e, van broeckhoven c. Am J Pathol. 2002 Aug;161(2):507-20. doi: 10.1016/S0002-9440(10)64207-1. Am J Pathol. 2002. PMID: 12163376 Free PMC article.
A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths.
Nelis E, Erdem S, Tan E, Löfgren A, Ceuterick C, De Jonghe P, Van Broeckhoven C, Timmerman V, Topaloglu H. Nelis E, et al. Among authors: van broeckhoven c. Neuromuscul Disord. 2002 Nov;12(9):869-73. doi: 10.1016/s0960-8966(02)00046-9. Neuromuscul Disord. 2002. PMID: 12398840 Clinical Trial.
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.
Dermaut B, Croes EA, Rademakers R, Van den Broeck M, Cruts M, Hofman A, van Duijn CM, Van Broeckhoven C. Dermaut B, et al. Among authors: van duijn cm, van den broeck m, van broeckhoven c. Ann Neurol. 2003 Mar;53(3):409-12. doi: 10.1002/ana.10507. Ann Neurol. 2003. PMID: 12601712
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