Search Results - "Berg, L. H."
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Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4
Published in European journal of neurology (01-03-2018)“…Background and purpose Natural history studies in spinal muscular atrophy (SMA) have primarily focused on infants and children. Natural history studies…”
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2
A comparative study of brachial plexus sonography and magnetic resonance imaging in chronic inflammatory demyelinating neuropathy and multifocal motor neuropathy
Published in European journal of neurology (01-10-2017)“…Background and purpose To compare the performance of neuroimaging techniques, i.e. high‐resolution ultrasound (HRUS) and magnetic resonance imaging (MRI), when…”
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3
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…”
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4
Cardiac pathology in spinal muscular atrophy: a systematic review
Published in Orphanet journal of rare diseases (11-04-2017)“…Hereditary proximal spinal muscular atrophy (SMA) is a severe neuromuscular disease of childhood caused by homozygous loss of function of the survival motor…”
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Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy
Published in Neurology (31-08-2010)“…Identification and examination of all patients with multifocal motor neuropathy (MMN) in the Netherlands to document the clinical spectrum and response to IV…”
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Instrumented assessment of lower and upper motor neuron signs in amyotrophic lateral sclerosis using robotic manipulation: an explorative study
Published in Journal of neuroengineering and rehabilitation (29-10-2024)“…Amyotrophic lateral sclerosis (ALS) is a lethal progressive neurodegenerative disease characterized by upper motor neuron (UMN) and lower motor neuron (LMN)…”
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7
Prose memory impairment in amyotrophic lateral sclerosis patients is related to hippocampus volume
Published in European journal of neurology (01-03-2015)“…Background and purpose Thirty per cent of amyotrophic lateral sclerosis (ALS) patients have non‐motor symptoms, including executive and memory deficits. The in…”
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A natural history study of late onset spinal muscular atrophy types 3b and 4
Published in Journal of neurology (01-09-2008)“…Background Spinal muscular atrophy (SMA) is caused by a homozygous deletion of the survival motor neuron (SMN)1 gene. The nearly identical SMN2 gene plays a…”
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9
Multidisciplinary ALS care improves quality of life in patients with ALS
Published in Neurology (25-10-2005)“…To examine the effect of multidisciplinary ALS care on the quality-of-life (QoL) in patients with ALS and their caregivers. In a cross-sectional study, 208…”
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10
Ultrasonography shows extensive nerve enlargements in multifocal motor neuropathy
Published in Neurology (26-07-2005)“…Using ultrasonography we found multiple sites with nerve enlargement along the course of the brachial plexus, median, ulnar, and radial nerves in the majority…”
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11
No association between Borrelia burgdorferi antibodies and amyotrophic lateral sclerosis in a case–control study
Published in European journal of neurology (01-01-2017)“…Background and purpose Previous studies, mostly case reports and uncontrolled studies, provide a low level of evidence for the hypothesized link between Lyme…”
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12
Correlation of the patient's reported outcome Inflammatory-RODS with an objective metric in immune-mediated neuropathies
Published in European journal of neurology (01-07-2016)“…Background and purpose There is increasing interest in using patient‐reported outcome measures (PROMs) in clinical studies to capture individual changes over…”
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13
Composite endpoint for ALS clinical trials based on patient preference: Patient-Ranked Order of Function (PROOF)
Published in Journal of neurology, neurosurgery and psychiatry (01-05-2022)“…BackgroundPatients with amyotrophic lateral sclerosis (ALS) show considerable variation in symptoms. Treatments targeting an overall improvement in…”
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14
SMN1 gene duplications are associated with sporadic ALS
Published in Neurology (13-03-2012)“…To investigate the role of SMN1 and SMN2 copy number variation and point mutations in amyotrophic lateral sclerosis (ALS) pathogenesis in a large population…”
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15
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
Published in Neurology (04-11-2008)“…To investigate the frequency of autosomal recessive paraplegin mutations in patients with sporadic adult-onset upper motor neuron (UMN) syndromes. We analyzed…”
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16
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
Published in Neurology (22-07-2008)“…Null mutations in progranulin (PGRN) cause ubiquitin-positive frontotemporal dementia (FTD) linked to chromosome 17q21 (FTDU-17). Here we examined PGRN genetic…”
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17
Diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow
Published in Neurology (09-03-2004)“…To determine the diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow (UNE). Sonographic ulnar nerve diameter measurement was…”
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18
Diagnostic accuracy of nerve excitability and compound muscle action potential scan derived biomarkers in amyotrophic lateral sclerosis
Published in European journal of neurology (01-10-2023)“…The lack of reliable early biomarkers still causes substantial diagnostic delays in amyotrophic lateral sclerosis (ALS). The aim was to assess the diagnostic…”
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19
Trends and determinants of end-of-life practices in ALS in the Netherlands
Published in Neurology (22-09-2009)“…In the Netherlands, the proportion of patients with amyotrophic lateral sclerosis (ALS) who choose the option of euthanasia or physician-assisted suicide (PAS)…”
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20
Lifetime occupation, education, smoking, and risk of ALS
Published in Neurology (09-10-2007)“…To investigate the association between cigarette smoking, level of education, occupation, and the occurrence of sporadic amyotrophic lateral sclerosis (ALS). A…”
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