Biomarkers in motor neuron disease: a state of the art review
NS Verber, SR Shepheard, M Sassani… - Frontiers in …, 2019 - frontiersin.org
Motor neuron disease can be viewed as an umbrella term describing a heterogeneous
group of conditions, all of which are relentlessly progressive and ultimately fatal. The …
group of conditions, all of which are relentlessly progressive and ultimately fatal. The …
[HTML][HTML] Prevalence, causes, and complications of cesarean delivery in Iran: A systematic review and meta-analysis
M Rafiei, MS Ghare, M Akbari, F Kiani… - International journal …, 2018 - ncbi.nlm.nih.gov
Background: Uncontrolled increase of C-section is one of the major problems in Iranian
health system, such that C-section is the most common surgical procedure in the entire …
health system, such that C-section is the most common surgical procedure in the entire …
[HTML][HTML] Fluid-based biomarkers for amyotrophic lateral sclerosis
LT Vu, R Bowser - Neurotherapeutics, 2017 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a highly heterogeneous disease with no effective
treatment. Drug development has been hampered by the lack of biomarkers that aid in early …
treatment. Drug development has been hampered by the lack of biomarkers that aid in early …
From multi-omics approaches to precision medicine in amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disorder,
caused by the degeneration of upper and lower motor neurons for which there is no truly …
caused by the degeneration of upper and lower motor neurons for which there is no truly …
Discovery of biomarkers for amyotrophic lateral sclerosis from human cerebrospinal fluid using mass-spectrometry-based proteomics
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease
characterized by the loss of upper and lower motor neurons, which eventually may lead to …
characterized by the loss of upper and lower motor neurons, which eventually may lead to …
Blood biomarkers for amyotrophic lateral sclerosis: myth or reality?
L Robelin… - BioMed research …, 2014 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a fatal condition primarily characterized by the
selective loss of upper and lower motor neurons. At present, the diagnosis and monitoring of …
selective loss of upper and lower motor neurons. At present, the diagnosis and monitoring of …
Plasma metabolomic biomarker panel to distinguish patients with amyotrophic lateral sclerosis from disease mimics
KA Lawton, MV Brown, D Alexander, Z Li… - … Lateral Sclerosis and …, 2014 - Taylor & Francis
Our objective was to identify plasma biomarkers of ALS that can aid in distinguishing
patients with ALS from those with disease mimics. In this multi-center study, plasma samples …
patients with ALS from those with disease mimics. In this multi-center study, plasma samples …
The extracellular domain of neurotrophin receptor p75 as a candidate biomarker for amyotrophic lateral sclerosis
Objective biomarkers for amyotrophic lateral sclerosis would facilitate the discovery of new
treatments. The common neurotrophin receptor p75 is up regulated and the extracellular …
treatments. The common neurotrophin receptor p75 is up regulated and the extracellular …
Discovery of Apo-A1 as a potential bladder cancer biomarker by urine proteomics and analysis
C Li, H Li, T Zhang, J Li, L Liu, J Chang - Biochemical and biophysical …, 2014 - Elsevier
Bladder cancer is clinically characterized by high recurrent rate and poor prognosis and
thereby patients need regular re-examinations which are invasive, unpleasant, and …
thereby patients need regular re-examinations which are invasive, unpleasant, and …
Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis
A Häggmark, M Mikus, A Mohsenchian… - Annals of clinical …, 2014 - Wiley Online Library
Objective Amyotrophic lateral sclerosis (ALS) is the most common adult motor neuron
disease leading to muscular paralysis and death within 3–5 years from onset. Currently …
disease leading to muscular paralysis and death within 3–5 years from onset. Currently …