Search Results - "van den Berg, L.H"

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    Cytokine profiles in multifocal motor neuropathy and progressive muscular atrophy by Vlam, L, Stam, M, de Jager, W, Cats, E.A, van den Berg, L.H, van der Pol, W.L

    Published in Journal of neuroimmunology (15-09-2015)
    “…Abstract Multifocal motor neuropathy (MMN) and progressive muscular atrophy (PMA) are associated with IgM monoclonal gammopathy or the presence IgM…”
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    Journal Article
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    Sexual differences in onset of disease and response to exercise in a transgenic model of ALS by Veldink, J.H., Bär, P.R., Joosten, E.A.J., Otten, M., Wokke, J.H.J., van den Berg, L.H.

    Published in Neuromuscular disorders : NMD (01-11-2003)
    “…Transgenic mice that overexpress the mutant human SOD1 gene (hSOD1) serve as an animal model for amyotrophic lateral sclerosis (ALS). Age and sex are…”
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    G.P.290 by Raaphorst, J, van Tol, M.J, de Groot, P.F.C, Altena, E, van der Werf, Y.D, Majoie, C.B, van der Kooi, A.J, van den Berg, L.H, Schmand, B.A, de Visser, M, Veltman, D.J

    Published in Neuromuscular disorders : NMD (01-10-2014)
    “…We aimed to examine brain activation patterns during verbal fluency performance in patients with progressive muscular atrophy (PMA) and amyotrophic lateral…”
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    G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3 by Van der Pol, W.L, Wadman, R.I, Van den Berg, L.H, Vrancken, A.F.J

    Published in Neuromuscular disorders : NMD (01-10-2012)
    “…Abstract Degeneration of the alpha motor neurons in the spinal cord is the pathological hallmark of SMA. Recent pathological studies in mouse models of SMA…”
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    Variations in ventral root axon morphology and locomotor behavior components across different inbred strains of mice by de Mooij-van Malsen, J.G, Yu, K.L, Veldman, H, Oppelaar, H, van den Berg, L.H, Olivier, B, Kas, M.J.H

    Published in Neuroscience (29-12-2009)
    “…Abstract Locomotion is a complex behavior affected by many different brain- and spinal cord systems, as well as by variations in the peripheral nervous system…”
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    Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS by VELDINK, J. H, VAN DEN BERG, L. H, COBBEN, J. M, STULP, R. P, DE JONG, J. M. B. V, VOGELS, O. J, BAAS, F, WOKKE, J. H. J, SCHEFFER, H

    Published in Neurology (27-03-2001)
    “…Spinal muscular atrophy (SMA) results from mutations of the survival motor neuron (SMN) gene on chromosome 5. The SMN gene exists in two highly homologous…”
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    Increased glutamine synthetase but normal EAAT2 expression in platelets of ALS patients by Bos, I.W.M., Hoogland, G., Meine Jansen, C.F., Willigen, G. van, Spierenburg, H.A., van den Berg, L.H., de Graan, P.N.E.

    Published in Neurochemistry international (01-03-2006)
    “…Amyotrophic lateral sclerosis is a fatal neurodegenerative disease and glutamate excitotoxicity has been implicated in its pathogenesis. Platelets contain a…”
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    HP19: Preliminary evidence of neurophysiological changes in asymptomatic carriers of the C9orf72 gene mutation using EEG by Dukic, S., Sleutjes, B.T.H., Nasseroleslami, B., Hardiman, O., Van Den Berg, L.H.

    Published in Clinical neurophysiology (01-03-2022)
    “…Cognitive and behavioural changes as well as dysfunctional brain metabolism and structural degeneration have been reported in asymptomatic carriers of the…”
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    Zinc amplifies mSOD1-mediated toxicity in a transgenic mouse model of amyotrophic lateral sclerosis by Groeneveld, G.J., de Leeuw van Weenen, J., van Muiswinkel, F.L., Veldman, H., Veldink, J.H., Wokke, J.H.J., Bär, P.R., van den Berg, L.H.

    Published in Neuroscience letters (11-12-2003)
    “…Transgenic mice overexpressing the human mutated form (G93A) of Cu,Zn-superoxide dismutase (mSOD1) develop motor neuron degeneration resembling amyotrophic…”
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    Pathogenicity of anti-ganglioside antibodies in the Guillain-Barré syndrome by van Sorge, N.M, van der Pol, W.-L, Jansen, M.D, van den Berg, L.H

    Published in Autoimmunity reviews (01-02-2004)
    “…Guillain-Barré syndrome (GBS) is a postinfectious inflammatory polyradiculo-neuropathy characterized by flaccid paralysis. Antibodies directed against…”
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    HP51 : Motor unit integrity in multifocal motor neuropathy: A systematic evaluation with CMAP scans by Stikvoort Garcia, D.J.L., Kovalchuck, M.O., Goedee, H.S., Van Schelven, L.J., Van Den Berg, L.H., Franssen, H., Sleutjes, B.T.H.M.

    Published in Clinical neurophysiology (01-03-2022)
    “…To systematically study the yield of CMAP scan recordings in a large sample of MMN patients. Introduction: We identified motor unit (MU) integrity in a large…”
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    OC07: Monitoring disease progression with electrophysiological markers derived from compound muscle action potential scans in amyotrophic lateral sclerosis by Sleutjes, B.T.H.M., Jacobsen, A.B., Tankisi, H., Sirin, N.G., Oge, A.E., Henderson, R.D., Van Doorn, P.A., Van Den Berg, L.H., Van Eijk, R.P.A.

    Published in Clinical neurophysiology (01-03-2022)
    “…To determine which electrophysiological markers derived from the compound muscle action potential (CMAP) scan are most sensitive to monitor disease progression…”
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    Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2 by VAN DAMME, P, VELDINK, J. H, VAN BLITTERSWIJK, M, CORVELEYN, A, VAN VUGHT, P. W. J, THIJS, V, DUBOIS, B, MATTHIJS, G, VAN DEN BERG, L. H, ROBBERECHT, W

    Published in Neurology (14-06-2011)
    “…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder of motor neurons that results in progressive muscle weakness and limits survival to 2-5…”
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    Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment by EFTIMOV, F, VERMEULEN, M, VAN DOORN, P. A, BRUSSE, E, VAN SCHAIK, I. N

    Published in Neurology (03-04-2012)
    “…Achieving long-term remission after a limited more intense treatment period would prevent prolonged use of corticosteroids or IV immunoglobulin (IVIg) in…”
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