Robberecht W - Search Results

1

Hdac6 deletion delays disease progression in the SOD1G93A mouse model of ALS.

Taes I, Timmers M, Hersmus N, Bento-Abreu A, Van Den Bosch L, Van Damme P, Auwerx J, Robberecht W. Taes I, et al. Among authors: robberecht w. Hum Mol Genet. 2013 May 1;22(9):1783-90. doi: 10.1093/hmg/ddt028. Epub 2013 Jan 30. Hum Mol Genet. 2013. PMID: 23364049 Free article.

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

Glial cells potentiate kainate-induced neuronal death in a motoneuron-enriched spinal coculture system.

Vandenberghe W, Van Den Bosch L, Robberecht W. Vandenberghe W, et al. Among authors: robberecht w. Brain Res. 1998 Oct 5;807(1-2):1-10. doi: 10.1016/s0006-8993(98)00569-1. Brain Res. 1998. PMID: 9756982

6

Tissue-type plasminogen activator is not required for kainate-induced motoneuron death in vitro.

Vandenberghe W, Van Den Bosch L, Robberecht W. Vandenberghe W, et al. Among authors: robberecht w. Neuroreport. 1998 Aug 24;9(12):2791-6. doi: 10.1097/00001756-199808240-00020. Neuroreport. 1998. PMID: 9760122

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

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

9

Calcium handling proteins in isolated spinal motoneurons.

Van Den Bosch L, Verhoeven K, De Smedt H, Wuytack F, Missiaen L, Robberecht W. Van Den Bosch L, et al. Among authors: robberecht w. Life Sci. 1999;65(15):1597-606. doi: 10.1016/s0024-3205(99)00405-1. Life Sci. 1999. PMID: 10574226

10

Abnormal intracellular ca(2+)homeostasis and disease.

Missiaen L, Robberecht W, van den Bosch L, Callewaert G, Parys JB, Wuytack F, Raeymaekers L, Nilius B, Eggermont J, De Smedt H. Missiaen L, et al. Among authors: robberecht w. Cell Calcium. 2000 Jul;28(1):1-21. doi: 10.1054/ceca.2000.0131. Cell Calcium. 2000. PMID: 10942700 Review.

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