Robberecht W - Search Results

1

Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease.

Philips T, Robberecht W. Philips T, et al. Among authors: robberecht w. Lancet Neurol. 2011 Mar;10(3):253-63. doi: 10.1016/S1474-4422(11)70015-1. Lancet Neurol. 2011. PMID: 21349440 Review.

2

Myasthenic syndrome caused by direct effect of chloroquine on neuromuscular junction.

Robberecht W, Bednarik J, Bourgeois P, van Hees J, Carton H. Robberecht W, et al. Arch Neurol. 1989 Apr;46(4):464-8. doi: 10.1001/archneur.1989.00520400124033. Arch Neurol. 1989. PMID: 2650665 Review.

3

Painful muscle spasms complicating algodystrophy: central or peripheral disease?

Robberecht W, Van Hees J, Adriaensen H, Carton H. Robberecht W, et al. J Neurol Neurosurg Psychiatry. 1988 Apr;51(4):563-7. doi: 10.1136/jnnp.51.4.563. J Neurol Neurosurg Psychiatry. 1988. PMID: 3379430 Free PMC article.

4

Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.

Verhalle D, Löfgren A, Nelis E, Dehaene I, Theys P, Lammens M, Dom R, Van Broeckhoven C, Robberecht W. Verhalle D, et al. Among authors: robberecht w. Ann Neurol. 1994 Jun;35(6):704-8. doi: 10.1002/ana.410350611. Ann Neurol. 1994. PMID: 8210227

5

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

6

Lymphocytic infundibulohypophysitis presenting in the postpartum period: case report.

Van Havenbergh T, Robberecht W, Wilms G, Van Calenbergh F, Goffin J, Dom R, Bouillon R, Plets C. Van Havenbergh T, et al. Among authors: robberecht w. Surg Neurol. 1996 Sep;46(3):280-4. doi: 10.1016/0090-3019(96)00215-7. Surg Neurol. 1996. PMID: 8781599

7

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

8

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

9

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

10

Copper and zinc levels in familial amyotrophic lateral sclerosis patients with CuZnSOD gene mutations.

Radunović A, Delves HT, Robberecht W, Tilkin P, Enayat ZE, Shaw CE, Stević Z, Apostolski S, Powell JF, Leigh PN. Radunović A, et al. Among authors: robberecht w. Ann Neurol. 1997 Jul;42(1):130-1. doi: 10.1002/ana.410420124. Ann Neurol. 1997. PMID: 9225698 No abstract available.

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