Advertisement

Topics

PubMed Journals Articles About "Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast" RSS

20:30 EST 18th February 2019 | BioPortfolio

Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast PubMed articles on BioPortfolio. Our PubMed references draw on over 21 million records from the medical literature. Here you can see the latest Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast articles that have been published worldwide.

More Information about "Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast" on BioPortfolio

We have published hundreds of Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast news stories on BioPortfolio along with dozens of Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast Clinical Trials and PubMed Articles about Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast Companies in our database. You can also find out about relevant Amyotrophic Lateral Sclerosis Market Insights Epidemiology Market Forecast Drugs and Medications on this site too.

Showing "Amyotrophic lateral sclerosis Market Insights Epidemiology Market Forecast" PubMed Articles 1–25 of 8,700+

Amyotrophic lateral sclerosis in Nordland county, Norway, 2000-2015: prevalence, incidence, and clinical features.

There are some indications of increasing incidence of amyotrophic lateral sclerosis (ALS). Awareness of cognitive impairment in ALS has increased in recent years. We describe the epidemiology and clinical features of ALS in a county in northern Norway over a period of 15 years.


Very late-onset amyotrophic lateral sclerosis in a Portuguese cohort.

Although amyotrophic lateral sclerosis (ALS) incidence has been stable among Western countries, population-ageing effect will probably increase the proportion of very-old ALS patients. We aim to study this population.

Cortico-efferent tract involvement in primary lateral sclerosis and amyotrophic lateral sclerosis: A two-centre tract of interest-based DTI analysis.

After the demonstration of a corticoefferent propagation pattern in amyotrophic lateral sclerosis (ALS) by neuropathological studies, this concept has been used for in vivo staging of individual patients by diffusion tensor imaging (DTI) techniques, both in `classical` ALS and in restricted phenotypes such as primary lateral sclerosis (PLS).


Dysfunction of attention switching networks in amyotrophic lateral sclerosis.

To localise and characterise changes in cognitive networks in Amyotrophic Lateral Sclerosis (ALS) using source analysis of mismatch negativity (MMN) waveforms.

Evaluation of Chitotriosidase and CC-Chemokine Ligand 18 as Biomarkers of Microglia Activation in Amyotrophic Lateral Sclerosis.

The development of biomarkers for use in diagnosing, monitoring disease progression and analyzing therapeutic trials response in amyotrophic lateral sclerosis (ALS) is essential.

Stem cell transplantation for amyotrophic lateral sclerosis.

This review analyses the recent efforts to develop therapeutics using transplantation of stem cells for amyotrophic lateral sclerosis (ALS).

Decremental Responses to Repetitive Nerve Stimulation in Amyotrophic Lateral Sclerosis.

To illuminate the mechanism of neuromuscular junction involvement by analyzing the features of a slow-rate repetitive nerve simulation (RNS) and EMG in amyotrophic lateral sclerosis (ALS) patients.

Moral judgment in patients with behavioral variant of frontotemporal dementia and amyotrophic lateral sclerosis: no impairment of the moral position, but rather its execution.

To investigate moral judgment competence in patients with the behavioral variant frontotemporal dementia (bvFTD) compared to amyotrophic lateral sclerosis (ALS) and controls.

Amyotrophic lateral sclerosis diagnostic index: Toward a personalized diagnosis of ALS.

The aim of the study was to assess the utility of a novel amyotrophic lateral sclerosis (ALS) diagnostic index (ALSDI).

Amyotrophic lateral sclerosis diagnostic index: Toward a personalized diagnosis of ALS.

The aim of the study was to assess the utility of a novel amyotrophic lateral sclerosis (ALS) diagnostic index (ALSDI).

The mathematics of market timing.

Market timing is an investment technique that tries to continuously switch investment into assets forecast to have better returns. What is the likelihood of having a successful market timing strategy? With an emphasis on modeling simplicity, I calculate the feasible set of market timing portfolios using index mutual fund data for perfectly timed (by hindsight) all or nothing quarterly switching between two asset classes, US stocks and bonds over the time period 1993-2017. The historical optimal timing path ...

Comparative assessment of limb function and conduction parameters in peripheral nerves in the course of two forms of amyotrophic lateral sclerosis.

Amyotrophic lateral sclerosis (ALS) is a progressive, incurable, neurodegenerative disease affecting the upper and lower motor neuron, which inevitably leads to the impaired fitness of patients and therefore deterioration of their quality of life.

Amyotrophic Lateral Sclerosis Mortality in the United States, 2011-2014.

The International Classification of Disease, 10th Revision (ICD-10) did not include a code specific for Amyotrophic lateral sclerosis (ALS) until 2017. Instead, code G12.2 included both ALS and other motor neuron diseases (MND). Our objective was to determine US mortality rates for ALS exclusively by excluding other MND and progressive supranuclear palsy.

Motor neuron-derived microRNAs cause astrocyte dysfunction in amyotrophic lateral sclerosis.

We recently demonstrated that microRNA-218 (miR-218) is greatly enriched in motor neurons and is released extracellularly in amyotrophic lateral sclerosis model rats. To determine if the released, motor neuron-derived miR-218 may have a functional role in amyotrophic lateral sclerosis, we examined the effect of miR-218 on neighbouring astrocytes. Surprisingly, we found that extracellular, motor neuron-derived miR-218 can be taken up by astrocytes and is sufficient to downregulate an important glutamate tran...

Response to Letter to the Editor: "Amyotrophic lateral sclerosis and exposure to diesel exhaust in a Danish cohort".

Longitudinal assessment of clinical and inflammatory markers in patients with amyotrophic lateral sclerosis.

To evaluate potential associations between clinical features and inflammatory markers in patients with amyotrophic lateral sclerosis (ALS).

Amyotrophic lateral sclerosis in Beijing: Epidemiologic features and prognosis from 2010 to 2015.

To determine the incidence of amyotrophic lateral sclerosis (ALS) in Beijing from 2010 to 2015 and to address the issue of prognosis.

Critical Review of Complementary and Alternative Medicine Use in Amyotrophic Lateral Sclerosis: Prevalence and Users' Profile, Decision-Making, Information Seeking, and Disclosure in the Face of a Lack of Efficacy.

Despite a lack of evidence of clinical efficacy for complementary and alternative medicine (CAM) use in amyotrophic lateral sclerosis (ALS), these medicines remain popular around the world.

Dyspnea in amyotrophic lateral sclerosis (ALS): Rasch-based development and validation of a patient-reported outcome (DALS-15).

Dyspnea is a cardinal but often underestimated symptom in amyotrophic lateral sclerosis (ALS). The lack of a satisfying assessment tool leads to diagnostic uncertainty and bears the risk that established life-prolonging and symptom relieving therapeutic options will not be adequately applied.

Effects of market type and time of purchase on oxidative status and descriptive off-odors and off-flavors of beef in Vietnam.

The objective of the current study was to determine the effects of market type (super market - SM, indoor market - IM, open market - OM) and sampling time (at the opening - T0 and 4 h after the opening - T4) on antioxidant capacity, lipid oxidation, and descriptive sensory attributes of beef in Vietnam. Values of FC and TEAC were greater in OM beef than IM and SM (P 

Impact of expiratory strength training in amyotrophic lateral sclerosis: Results of a randomized sham controlled trial.

The purpose of this study was to determine the impact of an in home expiratory muscle strength training (EMST) program on pulmonary, swallow and cough function in individuals with amyotrophic lateral sclerosis (ALS).

Repeated intrathecal mesenchymal stem cells for amyotrophic lateral sclerosis.

To assess the safety and efficacy of two repeated intrathecal injections of autologous bone marrow-derived mesenchymal stem cells (BM-MSCs) in amyotrophic lateral sclerosis (ALS).

50-Hz Magnetic Field Impairs the Expression of Iron-related Genes in the in vitro SOD1 Model of Amyotrophic Lateral Sclerosis.

we characterized the response to the extremely low frequency magnetic field (ELF-MF) in an in vitro model of familial Amyotrophic Lateral Sclerosis (fALS), carrying two mutant variants of the superoxide dismutase 1 (SOD1) gene.

Fasciculation intensity and disease progression in amyotrophic lateral sclerosis.

To investigate the association between the frequency and intensity of fasciculations with clinical measures of disease progression in amyotrophic lateral sclerosis (ALS).

Vestibular dysfunction as cortical damage with amyotrophic lateral sclerosis.

Cortical damage in areas such as the frontal lobe is reported in amyotrophic lateral sclerosis (ALS). However, aside from executive dysfunction, the pathological significance of this cortical damage has yet to be clarified. The present study investigated the effects of cortical damage on vestibular function in ALS.


Advertisement
Quick Search
Advertisement
Advertisement