Amyotrophic Lateral Sclerosis

Translation error tracked in the brain of dementia patients

In certain dementias silent areas of the genetic code are translated into highly unusual proteins by mistake. An international team of scientists including researchers from the German Center for Neurodegenerative ...

Neuroscience created Feb 07, 2013 | popularity 5 / 5 (1) | comments 0 | with audio podcast

Study confirms no transmission of Alzheimer's proteins between humans

A new study found no evidence to support concerns that abnormal neurodegenerative disease proteins are "infectious" or transmitted from animals to humans or from one person to another.

Alzheimer's disease & dementia created Feb 04, 2013 | popularity 3.7 / 5 (3) | comments 1 | with audio podcast

Eating bright-colored fruits and vegetables may prevent or delay ALS

New research suggests that increased consumption of foods containing colorful carotenoids, particularly beta-carotene and lutein, may prevent or delay the onset of amyotrophic lateral sclerosis (ALS). The study, published ...

Neuroscience created Jan 29, 2013 | popularity not rated yet | comments 0 | with audio podcast

Researchers identify new genetic mutation for ALS

Researchers at Western University in London, Canada, have identified a new genetic mutation for amyotrophic lateral sclerosis (ALS), opening the door to future targeted therapies. Dr. Michael Strong, a scientist ...

Genetics created Jan 15, 2013 | popularity not rated yet | comments 0

Scientists uncover potential drug target to block cell death in Parkinson's disease

Oxidative stress is a primary villain in a host of diseases that range from cancer and heart failure to Alzheimer's disease, Amyotrophic Lateral Sclerosis and Parkinson's disease. Now, scientists from the Florida campus of ...

Parkinson's & Movement disorders created Jan 10, 2013 | popularity 5 / 5 (1) | comments 0 | with audio podcast

Regulating single protein prompts fibroblasts to become neurons

Repression of a single protein in ordinary fibroblasts is sufficient to directly convert the cells – abundantly found in connective tissues – into functional neurons. The findings, which could have far-reaching ...

Medical research created Jan 10, 2013 | popularity 5 / 5 (2) | comments 0 | with audio podcast

Stem cells may hold promise for Lou Gehrig's disease

Apparent stem cell transplant success in mice may hold promise for people with amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease. The results of the study were released today and will be presented at the American ...

Neuroscience created Jan 09, 2013 | popularity 5 / 5 (2) | comments 0

A treatment for ALS? Neural stem cell transplants slow progression of disease

(Medical Xpress)—Results from a meta-analysis of 11 independent amyotrophic lateral sclerosis research studies are giving hope to the ALS community by showing, for the first time, that the fatal disease ...

Neuroscience created Jan 03, 2013 | popularity 5 / 5 (2) | comments 0 | with audio podcast

Removing protein 'garbage' in nerve cells may help control two neurodegenerative diseases

Neuroscientists at Georgetown University Medical Center say they have new evidence that challenges scientific dogma involving two fatal neurodegenerative diseases—amyotrophic lateral sclerosis (ALS), and frontotemporal ...

Medical research created Dec 20, 2012 | popularity 5 / 5 (6) | comments 0 | with audio podcast

New research discovery provides therapeutic target for ALS

Research led by Dr. Udai Pandey, Assistant Professor of Genetics at LSU Health Sciences Center New Orleans, has found that the ability of a protein made by a gene called FUS to bind to RNA is essential to the development ...

Genetics created Dec 19, 2012 | popularity 5 / 5 (2) | comments 0 | with audio podcast

Transplanted neural stem cells treat ALS in mouse model

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is untreatable and fatal. Nerve cells in the spinal cord die, eventually taking away a person's ability to move or even breathe. A ...

Medical research created Dec 19, 2012 | popularity 5 / 5 (4) | comments 0 | with audio podcast

Disruption of gene used to transport proteins leads to ALS

(Medical Xpress)—A Purdue University biochemist has determined the function of a gene that when mutated leads to a genetic variation of amyotrophic lateral sclerosis, or Lou Gehrig's disease.

Neuroscience created Dec 11, 2012 | popularity 5 / 5 (3) | comments 0 | with audio podcast

Researchers uncover toxic interaction in neurons that leads to dementia and ALS

Researchers at Mayo Clinic in Florida have uncovered a toxic cellular process by which a protein that maintains the health of neurons becomes deficient and can lead to dementia. The findings shed new light on the link between ...

Medical research created Dec 10, 2012 | popularity 5 / 5 (3) | comments 1 | with audio podcast

One gene predicts rapid ALS progression 80 percent of the time

(Medical Xpress)—The debilitating symptoms of amyotrophic lateral sclerosis, or ALS, appear to be increased by a lack of inflammation-reducing T cells, report scientists from the Methodist Neurological Institute in an upcoming ...

Genetics created Dec 10, 2012 | popularity 3 / 5 (1) | comments 0 | with audio podcast

See-through 'MitoFish' opens a new window on brain diseases

German scientists have demonstrated a new way to investigate mechanisms at work in Alzheimer's and other neurodegenerative diseases, which also could prove useful in the search for effective drugs. For new ...

Neuroscience created Dec 05, 2012 | popularity 5 / 5 (2) | comments 0 | with audio podcast


Amyotrophic lateral sclerosis (ALS), also referred to as Lou Gehrig's disease in American English and Motor Neurone Disease in British English, is a form of Motor Neuron Disease caused by the degeneration of upper and lower neurons, located in the ventral horn of the spinal cord and the cortical neurons that provide their efferent input. The condition is often called Lou Gehrig's disease in North America, after the New York Yankees baseball player who was diagnosed with the disease in 1939. The disorder is characterized by rapidly progressive weakness, muscle atrophy and fasciculations, spasticity, dysarthria, dysphagia, and respiratory compromise. Sensory function generally is spared, as is autonomic and oculomotor activity. ALS is a progressive, fatal, neurodegenerative disease with most affected patients dying of respiratory compromise and pneumonia after 2 to 3 years; although some perish within a year from the onset of symptoms, and occasional individuals have a more indolent course and survive for many years.

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