Robberecht W - Search Results

1

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

2

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

3

Distal myopathy as the presenting manifestation of sarcoidosis.

Robberecht W, Theys P, Lammens M, Leenders J. Robberecht W, et al. J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):642-3. doi: 10.1136/jnnp.59.6.642. J Neurol Neurosurg Psychiatry. 1995. PMID: 7500110 Free PMC article. No abstract available.

4

Neurocysticercosis: a poorly understood disease.

Vantomme M, Swartenbroekx R, Dhaen B, Peetermans W, Plets C, Demaerel P, Dom R, Robberecht W. Vantomme M, et al. Among authors: robberecht w. Acta Neurol Belg. 1995;95(1):23-8. Acta Neurol Belg. 1995. PMID: 7725893 Review.

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

Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP).

Timmerman V, Löfgren A, Le Guern E, Liang P, De Jonghe P, Martin JJ, Verhalle D, Robberecht W, Gouider R, Brice A, Van Broeckhoven C. Timmerman V, et al. Among authors: robberecht w. Hum Genet. 1996 Jan;97(1):26-34. doi: 10.1007/BF00218828. Hum Genet. 1996. PMID: 8557256

7

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

8

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

9

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

10

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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