Robberecht W - Search Results

1

Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis.

Philips T, Bento-Abreu A, Nonneman A, Haeck W, Staats K, Geelen V, Hersmus N, Küsters B, Van Den Bosch L, Van Damme P, Richardson WD, Robberecht W. Philips T, et al. Among authors: robberecht w. Brain. 2013 Feb;136(Pt 2):471-82. doi: 10.1093/brain/aws339. Epub 2013 Jan 31. Brain. 2013. PMID: 23378219 Free PMC article.

2

Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.

Robberecht W, Sapp P, Viaene MK, Rosen D, McKenna-Yasek D, Haines J, Horvitz R, Theys P, Brown R Jr. Robberecht W, et al. J Neurochem. 1994 Jan;62(1):384-7. doi: 10.1046/j.1471-4159.1994.62010384.x. J Neurochem. 1994. PMID: 8263541

3

Pathological findings in a patient with amyotrophic lateral sclerosis and multifocal motor neuropathy with conduction block.

Veugelers B, Theys P, Lammens M, Van Hees J, Robberecht W. Veugelers B, et al. Among authors: robberecht w. J Neurol Sci. 1996 Mar;136(1-2):64-70. doi: 10.1016/0022-510x(95)00295-d. J Neurol Sci. 1996. PMID: 8815180

4

D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis.

Robberecht W, Aguirre T, Van den Bosch L, Tilkin P, Cassiman JJ, Matthijs G. Robberecht W, et al. Neurology. 1996 Nov;47(5):1336-9. doi: 10.1212/wnl.47.5.1336. Neurology. 1996. PMID: 8909456

5

Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activity.

Robberecht W, Aguirre T, Van den Bosch L, Theys P, Nees H, Cassiman JJ, Matthijs G. Robberecht W, et al. Arch Neurol. 1997 Jan;54(1):46-50. doi: 10.1001/archneur.1997.00550130032012. Arch Neurol. 1997. PMID: 9006413

6

Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stress.

Aguirre T, Van Den Bosch L, Goetschalckx K, Tilkin P, Mathijs G, Cassiman JJ, Robberecht W. Aguirre T, et al. Among authors: robberecht w. Ann Neurol. 1998 Apr;43(4):452-7. doi: 10.1002/ana.410430407. Ann Neurol. 1998. PMID: 9546325

7

Glial cells potentiate kainate-induced neuronal death in a motoneuron-enriched spinal coculture system.

Vandenberghe W, Van Den Bosch L, Robberecht W. Vandenberghe W, et al. Among authors: robberecht w. Brain Res. 1998 Oct 5;807(1-2):1-10. doi: 10.1016/s0006-8993(98)00569-1. Brain Res. 1998. PMID: 9756982

8

Tissue-type plasminogen activator is not required for kainate-induced motoneuron death in vitro.

Vandenberghe W, Van Den Bosch L, Robberecht W. Vandenberghe W, et al. Among authors: robberecht w. Neuroreport. 1998 Aug 24;9(12):2791-6. doi: 10.1097/00001756-199808240-00020. Neuroreport. 1998. PMID: 9760122

9

Evolution of motor and sensory deficits in amyotrophic lateral sclerosis estimated by neurophysiological techniques.

Theys PA, Peeters E, Robberecht W. Theys PA, et al. Among authors: robberecht w. J Neurol. 1999 Jun;246(6):438-42. doi: 10.1007/s004150050379. J Neurol. 1999. PMID: 10431767

10

Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.

Aguirre T, Matthijs G, Robberecht W, Tilkin P, Cassiman JJ. Aguirre T, et al. Among authors: robberecht w. Eur J Hum Genet. 1999 Jul;7(5):599-602. doi: 10.1038/sj.ejhg.5200337. Eur J Hum Genet. 1999. PMID: 10439968

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