by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
TeleEMG Interview What is Lou Gehrig's disease or ALS amyotrophic lateral sclerosis 20151012Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment:...
by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
chinese medicine, neuron disease, amyotrophic lateral sclerosisPrognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction modelAmyotrophic lateral sclerosis is a relentlessly progressive, fatal motor neuron...
by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis (ALS)Oculomotor Dysfunction in Amyotrophic Lateral Sclerosis: A Comprehensive ReviewAlthough traditionally regarded as spared, a range of oculomotor dysfunction has been recorded in patients with amyotrophic lateral sclerosis. The...
by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is curable!Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosisIn summary, we report widespread mislocalization of the FUS protein in ALS and propose a putative underlying mechanism for this...
by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
Top 5 ALS FactsAmyotrophic lateral sclerosisWhile the peak age of onset is 58 to 63 for sporadic ALS and 47 to 52 for familial ALS, about 10% of all cases of ALS begin before age 45, and about 1% of all cases begin before age 25. Juvenile ALS is more likely to be...
by admin | Oct 22, 2019 | amyotrophic lateral sclerosis
ALS (amyotrophic lateral sclerosis) 5 month updateDisrupted neuronal trafficking in amyotrophic lateral sclerosisCorrectly folded proteins leave the ER at specialized sites called ER exit sites via coat protein complex II-coated vesicles and form tubular-like...
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