Search Results - "van den Berg, L.H"
-
1
Inhibition of HERV-K (HML-2) in amyotrophic lateral sclerosis patients on antiretroviral therapy
Published in Journal of the neurological sciences (15-04-2021)“…Reactivation of Human Endogenous Retrovirus K (HERV-K), subtype HML-2, has been associated with pathophysiology of amyotrophic lateral sclerosis (ALS). We…”
Get full text
Journal Article -
2
Cytokine profiles in multifocal motor neuropathy and progressive muscular atrophy
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…”
Get full text
Journal Article -
3
Sexual differences in onset of disease and response to exercise in a transgenic model of ALS
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…”
Get full text
Journal Article -
4
P12-18 Exercise-induced weakness in demyelinating neuropathies
Published in Clinical neurophysiology (2010)Get full text
Journal Article -
5
G.P.290
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…”
Get full text
Journal Article -
6
G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3
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…”
Get full text
Journal Article -
7
P3.6 Segmental distribution of muscle weakness in Dutch patients with SMA type 2, 3 and 4
Published in Neuromuscular disorders : NMD (01-10-2011)Get full text
Journal Article -
8
P12-19 Cold paresis in multifocal motor neuropathy
Published in Clinical neurophysiology (2010)Get full text
Journal Article -
9
Variations in ventral root axon morphology and locomotor behavior components across different inbred strains of mice
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…”
Get full text
Journal Article -
10
Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
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…”
Get full text
Journal Article -
11
Increased glutamine synthetase but normal EAAT2 expression in platelets of ALS patients
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…”
Get full text
Journal Article -
12
HP19: Preliminary evidence of neurophysiological changes in asymptomatic carriers of the C9orf72 gene mutation using EEG
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…”
Get full text
Journal Article -
13
Zinc amplifies mSOD1-mediated toxicity in a transgenic mouse model of amyotrophic lateral sclerosis
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…”
Get full text
Journal Article -
14
Pathogenicity of anti-ganglioside antibodies in the Guillain-Barré syndrome
Published in Autoimmunity reviews (01-02-2004)“…Guillain-Barré syndrome (GBS) is a postinfectious inflammatory polyradiculo-neuropathy characterized by flaccid paralysis. Antibodies directed against…”
Get full text
Journal Article -
15
HP51 : Motor unit integrity in multifocal motor neuropathy: A systematic evaluation with CMAP scans
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…”
Get full text
Journal Article -
16
OC07: Monitoring disease progression with electrophysiological markers derived from compound muscle action potential scans in amyotrophic lateral sclerosis
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…”
Get full text
Journal Article -
17
Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2
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…”
Get full text
Journal Article -
18
Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment
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…”
Get full text
Journal Article -
19
Neuro-imaging in amyotrophic lateral sclerosis: Should we shift towards the periphery?
Published in Clinical neurophysiology (01-09-2020)Get full text
Journal Article -
20
Corrigendum to ‘Associations between illness cognitions and health-related quality of life in the first year after diagnosis of amyotrophic lateral sclerosis’ [Journal of Psychosomatic Research 132 (2020) 109974]
Published in Journal of psychosomatic research (01-01-2021)Get full text
Journal Article