Robberecht W - Search Results

1

Progranulin genetic variability contributes to amyotrophic lateral sclerosis.

Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P, van Vught PW, van der Zee J, Serneels S, De Pooter T, Van den Broeck M, Cruts M, Schymkowitz J, De Jonghe P, Rousseau F, van den Berg LH, Robberecht W, Van Broeckhoven C. Sleegers K, et al. Among authors: robberecht w. Neurology. 2008 Jul 22;71(4):253-9. doi: 10.1212/01.wnl.0000289191.54852.75. Epub 2008 Jan 9. Neurology. 2008. PMID: 18184915

2

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

3

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

4

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

5

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.

6

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

7

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.

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

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.

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