Robberecht W - Search Results

1

Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2.

Van Damme P, Veldink JH, van Blitterswijk M, Corveleyn A, van Vught PW, Thijs V, Dubois B, Matthijs G, van den Berg LH, Robberecht W. Van Damme P, et al. Among authors: robberecht w. Neurology. 2011 Jun 14;76(24):2066-72. doi: 10.1212/WNL.0b013e31821f445b. Epub 2011 May 11. Neurology. 2011. PMID: 21562247

2

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

3

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

4

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

5

A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis. European ALS/IGF-I Study Group.

Borasio GD, Robberecht W, Leigh PN, Emile J, Guiloff RJ, Jerusalem F, Silani V, Vos PE, Wokke JH, Dobbins T. Borasio GD, et al. Among authors: robberecht w. Neurology. 1998 Aug;51(2):583-6. doi: 10.1212/wnl.51.2.583. Neurology. 1998. PMID: 9710040 Clinical Trial.

6

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

7

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

8

A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.

Tabaku M, Legius E, Robberecht W, Sciot R, Fryns JP, Cassiman JJ, Matthijs G. Tabaku M, et al. Among authors: robberecht w. Genet Couns. 1999;10(3):285-93. Genet Couns. 1999. PMID: 10546101

9

Oxidative stress in amyotrophic lateral sclerosis.

Robberecht W. Robberecht W. J Neurol. 2000 Mar;247 Suppl 1:I1-6. doi: 10.1007/s004150050551. J Neurol. 2000. PMID: 10795881 Review.

10

Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis population.

Thijs V, Peeters E, Theys P, Matthijs G, Robberecht W. Thijs V, et al. Among authors: robberecht w. Acta Neurol Belg. 2000 Jun;100(2):84-90. Acta Neurol Belg. 2000. PMID: 10934559

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