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269 results
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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
Purulent meningitis due to aspergillosis in a patient with systemic lupus erythematosus.
Lammens M, Robberecht W, Waer M, Carton H, Dom R. Lammens M, et al. Among authors: robberecht w. Clin Neurol Neurosurg. 1992;94(1):39-43. doi: 10.1016/0303-8467(92)90117-l. Clin Neurol Neurosurg. 1992. PMID: 1321697
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.
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.
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
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
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
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
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
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
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