Robberecht, Wim
Universitair Ziekenhuis Leuven · KU Leuven
10 papers on CoChat
Most cited papers
- Verified
The changing scene of amyotrophic lateral sclerosis
Robberecht, W., & Philips, T. (2013) · Nature Reviews Neuroscience
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 957
- Verified
Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease
Philips, T., & Robberecht, W. (2011) · The Lancet Neurology
Amyotrophic Lateral Sclerosis ResearchNeuroinflammation and Neurodegeneration Mechanisms
Cited by 646
- Verified
Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS
Jovičić, A., Mertens, J., Boeynaems, S., Bogaert, E., Chai, N., Yamada, S. B., Paul, J. W., Sun, S., Herdy, J. R., Bieri, G., et al. (2015) · Nature Neuroscience
Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases
Cited by 598
- Verified
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patients
Guo, W., Naujock, M., Fumagalli, L., Vandoorne, T., Baatsen, P., Boon, R., Ordovás, L., Patel, A., Welters, M., Vanwelden, T., et al. (2017) · Nature Communications
Amyotrophic Lateral Sclerosis ResearchPluripotent Stem Cells Research
Cited by 373
- Verified
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
Boeynaems, S., Bogaert, E., Michiels, E., Gijselinck, I., Sieben, A., Jovičić, A., De Baets, G., Scheveneels, W., Steyaert, J., Cuijt, I., et al. (2016) · Scientific Reports
Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases
Cited by 262
- Verified
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
Gijselinck, I., Van Mossevelde, S., van der Zee, J., Sieben, A., Philtjens, S., Heeman, B., Engelborghs, S., Vandenbulcke, M., De Baets, G., Bäumer, V., et al. (2015) · Neurology
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 174
- Verified
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
Sleegers, K., Brouwers, N., Maurer-Stroh, S., van Es, M. A., Damme, P. V., van Vught, P. W. J., van der Zee, J., Serneels, S., Pooter, T. D., Van den Broeck, M., et al. (2008) · Neurology
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 161
- Verified
Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo
Beel, S., Moisse, M., Damme, M., De Muynck, L., Robberecht, W., Van Den Bosch, L., Saftig, P., & Van Damme, P. (2017) · Human Molecular Genetics
Amyotrophic Lateral Sclerosis ResearchNerve injury and regeneration
Cited by 146
- Verified
Inhibition of p38 mitogen activated protein kinase activation and mutant SOD1G93A-induced motor neuron death
Dewil, M., dela Cruz, V. F., Van Den Bosch, L., & Robberecht, W. (2007) · Neurobiology of Disease
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 133
- Verified
A phase II–III trial of olesoxime in subjects with amyotrophic lateral sclerosis
Lenglet, T., Lacomblez, L., Abitbol, J. L., Ludolph, A., Mora, J. S., Robberecht, W., Shaw, P. J., Pruss, R. M., Cuvier, V., Meininger, V., et al. (2014) · European Journal of Neurology
Amyotrophic Lateral Sclerosis ResearchNeurogenetic and Muscular Disorders Research
Cited by 130
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