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期刊名:Amyotrophic lateral sclerosis

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ISSN:1748-2968

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共收录本刊相关文章索引99
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
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Maud Maessen,Marcel W Post,Rianne Maillé et al. Maud Maessen et al.
The objective was to validate the Dutch translation of the 40-item and 5-item Amyotrophic Lateral Sclerosis Assessment Questionnaire (ALSAQ-40, ALSAQ-5). Eighty-one ALS patients participated in this cross-sectional study. The measures used ...
Crispin Jenkinson,Robert Harris,Ray Fitzpatrick Crispin Jenkinson
The Amyotrophic Lateral Sclerosis Assessment Questionnaire (ALSAQ-40) is the most widely validated measure of health status for use with patients diagnosed with motor neuron disease/amyotrophic lateral sclerosis (MND/ALS). The questionnaire...
Eric J Sorenson,Brian Crum,J Clarke Stevens Eric J Sorenson
Aspiration pneumonia is believed to be an uncommon complication of amyotrophic lateral sclerosis (ALS). However, the incidence of aspiration pneumonia and its contribution to morbidity and mortality are unknown in ALS. All cases of ALS from...
Nathan Oates,Roger Pamphlett Nathan Oates
Epigenetic silencing of a gene vital for motor neuron function could underlie sporadic ALS. We therefore examined the methylation status of two genes, SOD1 and VEGF, which are implicated in ALS. Methylation in the promoters of these genes w...
Priti Y Ramamohan,M Gourie-Devi,A Nalini et al. Priti Y Ramamohan et al.
We have previously shown in our laboratory that cerebrospinal fluid from ALS patients (ALS-CSF) contains putative toxic factor(s). In the present study we determined the effect of ALS-CSF on the integrity of the Golgi apparatus of spinal mo...
Hyun Young Kim,Chang-Seok Ki,Seong-Ho Koh et al. Hyun Young Kim et al.
Familial ALS (FALS) is mostly inherited as an age-dependent autosomal dominant trait. Since the discovery of mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1), testing for SOD1 gene mutations has become a routine part of the ...
Steven O A Oluwole,Yuanrong Yao,Sebastian Conradi et al. Steven O A Oluwole et al.
Retroviral components of both exogenous and endogenous origins have been associated with nervous system diseases in both animals and humans. In the present study, the levels of transcripts from elements in the human endogenous retrovirus (H...
Eric J Sorenson,Christopher J Klein Eric J Sorenson
X-linked spinal and bulbar muscular atrophy (SBMA or Kennedy's disease) has a variable prognosis. Most male carriers are affected by their fourth or fifth decade of life, while some remain asymptomatic lifelong. Elevations of serum creatine...
Alison B Grossman,Susan Woolley-Levine,Walter G Bradley et al. Alison B Grossman et al.
Cognitive impairment in patients with amyotrophic lateral sclerosis (ALS) is well documented, but behavioral abnormalities are not well defined. The Frontal Systems Behavior Scale (FrSBe) was used to assess changes in apathy, disinhibition,...
Dara Meldrum,Eibhlis Cahalane,Ronan Conroy et al. Dara Meldrum et al.
Maximum voluntary isometric contraction (MVIC) is a standardized method for measurement of muscle strength in patients with neuromuscular disease. Values obtained from MVIC testing are difficult to interpret at present as normative data are...