Dideberg V - Search Results

1

Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients.

Uwineza A, Hitayezu J, Murorunkwere S, Ndinkabandi J, Kalala Malu CK, Caberg JH, Dideberg V, Bours V, Mutesa L. Uwineza A, et al. Among authors: dideberg v. J Trop Pediatr. 2014 Apr;60(2):112-7. doi: 10.1093/tropej/fmt090. Epub 2013 Nov 7. J Trop Pediatr. 2014. PMID: 24213305

2

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.

Uwineza A, Caberg JH, Hitayezu J, Hellin AC, Jamar M, Dideberg V, Rusingiza EK, Bours V, Mutesa L. Uwineza A, et al. Among authors: dideberg v. BMC Med Genet. 2014 Jul 12;15:79. doi: 10.1186/1471-2350-15-79. BMC Med Genet. 2014. PMID: 25016475 Free PMC article.

3

Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapy.

Beckers P, Caberg JH, Dideberg V, Dangouloff T, den Dunnen JT, Bours V, Servais L, Boemer F. Beckers P, et al. Among authors: dideberg v. Sci Rep. 2021 Feb 4;11(1):3011. doi: 10.1038/s41598-021-82725-z. Sci Rep. 2021. PMID: 33542429 Free PMC article.

4

Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX Deletion.

Petignot S, Daly AF, Castermans E, Korpershoek E, Scagnol I, Beckers P, Dideberg V, Rohmer V, Bours V, Beckers A. Petignot S, et al. Among authors: dideberg v. Horm Metab Res. 2020 Nov;52(11):784-787. doi: 10.1055/a-1186-0790. Epub 2020 Jun 10. Horm Metab Res. 2020. PMID: 32521546

5

[Integration of pharmacogenetics in the medical practice].

Dideberg V, Bours V. Dideberg V, et al. Rev Med Liege. 2005 Dec;60(12):918-22. Rev Med Liege. 2005. PMID: 16457391 Free article. Review. French.

6

Modulating effect of COMT Val(158)Met polymorphism on interference resolution during a working memory task.

Jaspar M, Dideberg V, Bours V, Maquet P, Collette F. Jaspar M, et al. Among authors: dideberg v. Brain Cogn. 2015 Apr;95:7-18. doi: 10.1016/j.bandc.2015.01.013. Epub 2015 Feb 12. Brain Cogn. 2015. PMID: 25682348 Free article.

7

Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference Resolution.

Jaspar M, Manard M, Dideberg V, Bours V, Maquet P, Collette F. Jaspar M, et al. Among authors: dideberg v. Cereb Cortex. 2016 Feb;26(2):498-509. doi: 10.1093/cercor/bhu188. Epub 2014 Sep 8. Cereb Cortex. 2016. PMID: 25205659 Free article.

8

Newborn screening for SMA in Southern Belgium.

Boemer F, Caberg JH, Dideberg V, Dardenne D, Bours V, Hiligsmann M, Dangouloff T, Servais L. Boemer F, et al. Among authors: dideberg v. Neuromuscul Disord. 2019 May;29(5):343-349. doi: 10.1016/j.nmd.2019.02.003. Epub 2019 Feb 15. Neuromuscul Disord. 2019. PMID: 31030938

9

[(S)un (M)ay (A)rise on SMA : the hope of a region without spinal muscular atrophy].

Boemer F, Caberg JH, Dideberg V, Beckers P, Marie S, Marcelis L, Bours V, Dangouloff T, Servais L. Boemer F, et al. Among authors: dideberg v. Rev Med Liege. 2019 Sep;74(9):461-464. Rev Med Liege. 2019. PMID: 31486315 Free article. French.

10

An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.

Dideberg V, Kristjansdottir G, Milani L, Libioulle C, Sigurdsson S, Louis E, Wiman AC, Vermeire S, Rutgeerts P, Belaiche J, Franchimont D, Van Gossum A, Bours V, Syvänen AC. Dideberg V, et al. Hum Mol Genet. 2007 Dec 15;16(24):3008-16. doi: 10.1093/hmg/ddm259. Epub 2007 Sep 19. Hum Mol Genet. 2007. PMID: 17881657 Free article.

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