Robberecht W - Search Results

1

Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke.

Lemmens R, Abboud S, Robberecht W, Vanhees L, Pandolfo M, Thijs V, Goris A. Lemmens R, et al. Among authors: robberecht w. Eur J Hum Genet. 2009 Oct;17(10):1287-93. doi: 10.1038/ejhg.2009.42. Epub 2009 Mar 25. Eur J Hum Genet. 2009. PMID: 19319159 Free PMC article.

2

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

3

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

4

Coexistence of CADASIL and Alzheimer's disease.

Thijs V, Robberecht W, De Vos R, Sciot R. Thijs V, et al. Among authors: robberecht w. J Neurol Neurosurg Psychiatry. 2003 Jun;74(6):790-2. doi: 10.1136/jnnp.74.6.790. J Neurol Neurosurg Psychiatry. 2003. PMID: 12754354 Free PMC article.

5

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death.

Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, Wyns S, Thijs V, Andersson J, van Marion I, Al-Chalabi A, Bornes S, Musson R, Hansen V, Beckman L, Adolfsson R, Pall HS, Prats H, Vermeire S, Rutgeerts P, Katayama S, Awata T, Leigh N, Lang-Lazdunski L, Dewerchin M, Shaw C, Moons L, Vlietinck R, Morrison KE, Robberecht W, Van Broeckhoven C, Collen D, Andersen PM, Carmeliet P. Lambrechts D, et al. Among authors: robberecht w. Nat Genet. 2003 Aug;34(4):383-94. doi: 10.1038/ng1211. Nat Genet. 2003. PMID: 12847526 Free article.

6

Influence of arterial input function on hypoperfusion volumes measured with perfusion-weighted imaging.

Thijs VN, Somford DM, Bammer R, Robberecht W, Moseley ME, Albers GW. Thijs VN, et al. Among authors: robberecht w. Stroke. 2004 Jan;35(1):94-8. doi: 10.1161/01.STR.0000106136.15163.73. Epub 2003 Dec 11. Stroke. 2004. PMID: 14671249

7

The G93C mutation in superoxide dismutase 1: clinicopathologic phenotype and prognosis.

Régal L, Vanopdenbosch L, Tilkin P, Van den Bosch L, Thijs V, Sciot R, Robberecht W. Régal L, et al. Among authors: robberecht w. Arch Neurol. 2006 Feb;63(2):262-7. doi: 10.1001/archneur.63.2.262. Arch Neurol. 2006. PMID: 16476815

8

Role of heat shock response and Hsp27 in mutant SOD1-dependent cell death.

Krishnan J, Lemmens R, Robberecht W, Van Den Bosch L. Krishnan J, et al. Among authors: robberecht w. Exp Neurol. 2006 Aug;200(2):301-10. doi: 10.1016/j.expneurol.2006.02.135. Epub 2006 Jun 27. Exp Neurol. 2006. PMID: 16806187

9

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response.

Dierick I, Irobi J, Janssens S, Theuns J, Lemmens R, Jacobs A, Corsmit E, Hersmus N, Van Den Bosch L, Robberecht W, De Jonghe P, Van Broeckhoven C, Timmerman V. Dierick I, et al. Among authors: robberecht w. Hum Mutat. 2007 Aug;28(8):830. doi: 10.1002/humu.9503. Hum Mutat. 2007. PMID: 17623484

10

Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish.

Lemmens R, Van Hoecke A, Hersmus N, Geelen V, D'Hollander I, Thijs V, Van Den Bosch L, Carmeliet P, Robberecht W. Lemmens R, et al. Among authors: robberecht w. Hum Mol Genet. 2007 Oct 1;16(19):2359-65. doi: 10.1093/hmg/ddm193. Epub 2007 Jul 17. Hum Mol Genet. 2007. PMID: 17636250

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