Robberecht W - Search Results

1

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

Fogh I, Lin K, Tiloca C, Rooney J, Gellera C, Diekstra FP, Ratti A, Shatunov A, van Es MA, Proitsi P, Jones A, Sproviero W, Chiò A, McLaughlin RL, Sorarù G, Corrado L, Stahl D, Del Bo R, Cereda C, Castellotti B, Glass JD, Newhouse S, Dobson R, Smith BN, Topp S, van Rheenen W, Meininger V, Melki J, Morrison KE, Shaw PJ, Leigh PN, Andersen PM, Comi GP, Ticozzi N, Mazzini L, D'Alfonso S, Traynor BJ, Van Damme P, Robberecht W, Brown RH, Landers JE, Hardiman O, Lewis CM, van den Berg LH, Shaw CE, Veldink JH, Silani V, Al-Chalabi A, Powell J. Fogh I, et al. Among authors: robberecht w. JAMA Neurol. 2016 Jul 1;73(7):812-20. doi: 10.1001/jamaneurol.2016.1114. JAMA Neurol. 2016. PMID: 27244217 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

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

4

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.

5

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

6

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.

7

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.

Al-Chalabi A, Andersen PM, Chioza B, Shaw C, Sham PC, Robberecht W, Matthijs G, Camu W, Marklund SL, Forsgren L, Rouleau G, Laing NG, Hurse PV, Siddique T, Leigh PN, Powell JF. Al-Chalabi A, et al. Among authors: robberecht w. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

8

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

9

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

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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