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Browsing by Author Ceulemans, B.
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2012 | A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA. | Vandeweyer, G.; Aa, N. van der; Ceulemans, B., et al |
| 2009 | Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome. | Aa, N. van der; Rooms, L.; Weyer, G. van de, et al |
| 2011 | Idebenone as a novel, therapeutic approach for Duchenne muscular dystrophy: results from a 12 month, double-blind, randomized placebo-controlled trial | Buyse, G.M.; Goemans, N.; Hauwe, M. van den, et al |
| 2012 | Novel infantile-onset leukoencephalopathy with high lactate level and slow improvement. | Steenweg, M.E.; Vanderver, A.; Ceulemans, B., et al |
| 2008 | REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. | Beetz, C.; Schule, R.; Deconinck, T., et al |
Showing results 1 to 5 of 5
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