Lou Gehrig's Disease News and Research

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Lou Gehrig's Disease or Amyotrophic Lateral Sclerosis (ALS) is a neurological disorder characterized by progressive degeneration of motor neuron cells in the spinal cord and brain, which ultimately results in paralysis and death. The disease takes its less-scientific name from Lou Gehrig, a baseball player with the New York Yankees in the late 1920s and 1930s, who was forced to retire in 1939 as a result of the loss of motor control caused by the disease.

In 1991, a team of researchers linked familial ALS to chromosome 21. Two years later, the SOD1 gene was identified as being associated with many cases of familial ALS. The enzyme coded for by SOD1 carries out a very important function in cells: it removes dangerous superoxide radicals by converting them into non-harmful substances. Defects in the action of this enzyme mean that the superoxide radicals attack cells from the inside, causing their death. Several different mutations in this enzyme all result in ALS, making the exact molecular cause of the disease difficult to ascertain.

Recent research has suggested that treatment with drugs called antioxidants may benefit ALS patients. However, since the molecular genetics of the disease are still unclear, a significant amount of research is still required to design other promising treatments for ALS.
FDA grants Neuralstem orphan drug designation for treatment of ALS with spinal cord stem cells

FDA grants Neuralstem orphan drug designation for treatment of ALS with spinal cord stem cells

CMD co-founder receives Prize4Life award for discovery of new ALS biomarker

CMD co-founder receives Prize4Life award for discovery of new ALS biomarker

Research shows nestin regulates formation of neuromuscular junction

Research shows nestin regulates formation of neuromuscular junction

Neuralstem ends litigation with ReNeuron

Neuralstem ends litigation with ReNeuron

ALS Biopharma receives ADDF grant to develop therapeutics against Alzheimer's disease

ALS Biopharma receives ADDF grant to develop therapeutics against Alzheimer's disease

Salk Institute uncovers presenilin's productive side

Salk Institute uncovers presenilin's productive side

Mutated TDP-43 can cause neurons to die: Study

Mutated TDP-43 can cause neurons to die: Study

Spirulina dietary supplement may provide clinical benefits for ALS patients

Spirulina dietary supplement may provide clinical benefits for ALS patients

FDA approves Neuralstem's IND to initiate NSI-189 Phase Ia safety trial in major depression

FDA approves Neuralstem's IND to initiate NSI-189 Phase Ia safety trial in major depression

SBUMC to rename and dedicate ALS clinic as Christopher Pendergast ALS Center of Excellence

SBUMC to rename and dedicate ALS clinic as Christopher Pendergast ALS Center of Excellence

Positive results from Neuraltus NP002 Phase 1/2 study for levodopa-induced dyskinesias in Parkinson's disease

Positive results from Neuraltus NP002 Phase 1/2 study for levodopa-induced dyskinesias in Parkinson's disease

New cerebrospinal fluid biomarkers to monitor Parkinson's disease

New cerebrospinal fluid biomarkers to monitor Parkinson's disease

Neuraltus reports positive results from NP001 Phase 1 study for ALS

Neuraltus reports positive results from NP001 Phase 1 study for ALS

Breakthrough with mutant gene that causes familial ALS

Breakthrough with mutant gene that causes familial ALS

New editorial dispel doubts about Lou Gehrig's ALS diagnosis

New editorial dispel doubts about Lou Gehrig's ALS diagnosis

Researchers discover NG2+ cells may impact ALS disease progression

Researchers discover NG2+ cells may impact ALS disease progression

Neuralstem files NSI-189 IND with FDA for Phase I safety trials for major depression

Neuralstem files NSI-189 IND with FDA for Phase I safety trials for major depression

New AAC devices can help patients with neurological conditions to communicate

New AAC devices can help patients with neurological conditions to communicate

Marker for aggressive form of idiopathic pulmonary fibrosis discovered

Marker for aggressive form of idiopathic pulmonary fibrosis discovered

Aestus receives $244,000 grant from QTDP program

Aestus receives $244,000 grant from QTDP program

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