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86 results

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Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.
Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C. Del-Favero J, et al. Among authors: van regenmorter n, van den bossche d, van broeckhoven c, van zand k. Hum Mol Genet. 1998 Feb;7(2):177-86. doi: 10.1093/hmg/7.2.177. Hum Mol Genet. 1998. PMID: 9425224
No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder.
Goossens D, Villafuerte S, Tissir F, Van Gestel S, Claes S, Souery D, Massat I, Van den Bossche D, Van Zand K, Mendlewicz J, Van Broeckhoven C, Del-Favero J. Goossens D, et al. Among authors: van gestel s, van den bossche d, van broeckhoven c, van zand k. Eur J Hum Genet. 2000 May;8(5):385-8. doi: 10.1038/sj.ejhg.5200469. Eur J Hum Genet. 2000. PMID: 10854100
Expanded RED products and loci containing CAG/CTG repeats on chromosome 17 (ERDA1) and chromosome 18 (CTG18.1) in trans-generational pairs with bipolar affective disorder.
Mendlewicz J, Souery D, Del-Favero J, Massat I, Lindblad K, Engström C, Van den Bossche D, Adolfsson R, Schalling M, Van Broeckhoven C. Mendlewicz J, et al. Among authors: van den bossche d, van broeckhoven c. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):71-5. doi: 10.1002/ajmg.b.20006. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211635
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Rademakers R, Melquist S, Cruts M, Theuns J, Del-Favero J, Poorkaj P, Baker M, Sleegers K, Crook R, De Pooter T, Bel Kacem S, Adamson J, Van den Bossche D, Van den Broeck M, Gass J, Corsmit E, De Rijk P, Thomas N, Engelborghs S, Heckman M, Litvan I, Crook J, De Deyn PP, Dickson D, Schellenberg GD, Van Broeckhoven C, Hutton ML. Rademakers R, et al. Among authors: van den broeck m, van den bossche d, van broeckhoven c. Hum Mol Genet. 2005 Nov 1;14(21):3281-92. doi: 10.1093/hmg/ddi361. Epub 2005 Sep 29. Hum Mol Genet. 2005. PMID: 16195395
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.
86 results