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1. Full Text Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease
by Philips, Thomas, MSc and Robberecht, Wim, Prof
Lancet neurology, ISSN 1474-4422, 2011, Volume 10, Issue 3, pp. 253 - 263
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amyotrophic Lateral Sclerosis - immunology | T-Lymphocytes - physiology | Inflammation - metabolism | Motor Neuron Disease - metabolism | Animals | Humans | Amyotrophic Lateral Sclerosis - metabolism | Motor Neuron Disease - immunology | Neuroglia - immunology | Neuroglia - metabolism | Signal Transduction - physiology | Inflammation - immunology | Index Medicus | Animal models | Parkinson's disease | Neurodegenerative diseases | Astrocytes | Therapeutic applications | Medical importance | Motor neuron disease | Transgenic mice | Amyotrophic lateral sclerosis | Inflammation | Neuronal-glial interactions | Microglial cells | Alzheimer's disease | Movement disorders
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2. Full Text The changing scene of amyotrophic lateral sclerosis
by Robberecht, Wim and Philips, Thomas
Nature reviews. Neuroscience, ISSN 1471-003X, 04/2013, Volume 14, Issue 4, pp. 248 - 264
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Frontotemporal Dementia - genetics | RNA-Binding Proteins - genetics | Animals | Amyotrophic Lateral Sclerosis - genetics | Humans | Amyotrophic Lateral Sclerosis - diagnosis | Amyotrophic Lateral Sclerosis - etiology | Frontotemporal Dementia - diagnosis | Mutation - genetics | Causes of | Complications and side effects | Amyotrophic lateral sclerosis | Development and progression | Care and treatment | Research | Index Medicus
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3. Full Text The phenotypic variability of amyotrophic lateral sclerosis
by Swinnen, Bart and Robberecht, Wim
Nature reviews. Neurology, ISSN 1759-4758, 11/2014, Volume 10, Issue 11, pp. 661 - 670
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Frontotemporal Dementia - genetics | Frontotemporal Dementia - physiopathology | Frontotemporal Dementia - complications | Phenotype | Amyotrophic Lateral Sclerosis - physiopathology | Amyotrophic Lateral Sclerosis - genetics | Humans | Frontotemporal Lobar Degeneration - genetics | Frontotemporal Lobar Degeneration - physiopathology | Disease Progression | Frontotemporal Lobar Degeneration - complications | Amyotrophic Lateral Sclerosis - complications | Care and treatment | Gene mutations | Patient outcomes | Analysis | Physiological aspects | Amyotrophic lateral sclerosis | Genetic aspects | Research | Index Medicus
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4. Full Text ELP3 Controls Active Zone Morphology by Acetylating the ELKS Family Member Bruchpilot
by Miśkiewicz, Katarzyna and Jose, Liya E and Bento-Abreu, André and Fislage, Marcus and Taes, Ines and Kasprowicz, Jarosław and Swerts, Jef and Sigrist, Stephan and Versées, Wim and Robberecht, Wim and Verstreken, Patrik
Neuron (Cambridge, Mass.), ISSN 0896-6273, 2011, Volume 72, Issue 5, pp. 776 - 788
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Embryo, Mammalian | Neuromuscular Junction - metabolism | Humans | Histone Acetyltransferases - genetics | Green Fluorescent Proteins - genetics | Presynaptic Terminals - ultrastructure | Drosophila Proteins - metabolism | Tubulin - metabolism | Transfection - methods | Histone Acetyltransferases - metabolism | Acetylation | Acetyltransferases | Microscopy, Electron, Transmission | Animals, Genetically Modified | Drosophila | Zebrafish | Presynaptic Terminals - physiology | Mutation - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Patch-Clamp Techniques | Animals | Larva | Drosophila Proteins - genetics | Cell Line, Transformed | Neuromuscular Junction - physiology | Histones | Neurons | DNA binding proteins | Proteins | Mutation | Grants | Insects | Cytoplasm | Index Medicus
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5. Full Text RNA toxicity in non‐coding repeat expansion disorders
by Swinnen, Bart and Robberecht, Wim and Van Den Bosch, Ludo
The EMBO journal, ISSN 0261-4189, 01/2020, Volume 39, Issue 1, pp. e101112 - n/a
C9ORF72 ALS/FTD | non‐coding repeat expansion disorders | RNA toxicity | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Tremor | Neurodegenerative diseases | Toxicity | Intellectual disabilities | Disorders | Amyotrophic lateral sclerosis | Nucleotides | Ribonucleic acid--RNA | Gene expression | Huntington's disease | Myotonic dystrophy | Coding | Dementia disorders | Ataxia | Dystrophy | Fragile X syndrome | Frontotemporal dementia | Expansion | Index Medicus | C9ORF72 ALS | Review | FTD
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