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Page 1
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts.
Van Langenhove T, van der Zee J, Engelborghs S, Vandenberghe R, Santens P, Van den Broeck M, Mattheijssens M, Peeters K, Nuytten D, Cras P, De Deyn PP, De Jonghe P, Cruts M, Van Broeckhoven C. Van Langenhove T, et al. Among authors: van den broeck m, van der zee j, van broeckhoven c. Neurobiol Aging. 2012 May;33(5):1004.e17-20. doi: 10.1016/j.neurobiolaging.2011.09.025. Epub 2011 Oct 27. Neurobiol Aging. 2012. PMID: 22035589
A chromosome 18 genetic linkage study in three large Belgian pedigrees with bipolar disorder.
Claes S, Raeymaekers P, Van den Broeck M, Diependaele S, De bruyn A, Verheyen G, Wils V, Boogaerts A, Tanghe A, Godderis J, Van Broeckhoven C, Cassiman JJ. Claes S, et al. Among authors: van den broeck m, van broeckhoven c. J Affect Disord. 1997 May;43(3):195-205. doi: 10.1016/s0165-0327(97)01429-8. J Affect Disord. 1997. PMID: 9186790
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease.
Cruts M, van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Hofman A, Van Broeckhoven C. Cruts M, et al. Among authors: van duijn cm, van den broeck m, van broeckhoven c. Hum Mol Genet. 1998 Jan;7(1):43-51. doi: 10.1093/hmg/7.1.43. Hum Mol Genet. 1998. PMID: 9384602
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 TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.
Theuns J, Feuk L, Dermaut B, Del-Favero J, Roks G, Van den Bossche D, Corsmit E, Van den Broeck M, van Duijn CM, Cruts M, Brookes AJ, Van Broeckhoven C. Theuns J, et al. Among authors: van duijn cm, van den broeck m, van den bossche d, van broeckhoven c. Hum Genet. 2001 Jun;108(6):552-3. doi: 10.1007/s004390100508. Hum Genet. 2001. PMID: 11499683 No abstract available.
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.
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
Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects.
Engelborghs S, Dermaut B, Goeman J, Saerens J, Mariën P, Pickut BA, Van den Broeck M, Serneels S, Cruts M, Van Broeckhoven C, De Deyn PP. Engelborghs S, et al. Among authors: van den broeck m, van broeckhoven c. J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1148-51. doi: 10.1136/jnnp.74.8.1148. J Neurol Neurosurg Psychiatry. 2003. PMID: 12876259 Free PMC article.
70 results