News tagged with muscular atrophy
Researchers identify drug candidate for treating spinal muscular atrophy
Nov 04, 2009 |
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A chemical cousin of the common antibiotic tetracycline might be useful in treating spinal muscular atrophy (SMA), a currently incurable disease that is the leading genetic cause of death in infants. This is the finding of ...
Mighty mice: Treatment targeted to muscle improves motor neuron disease
Medicine & Health / Neuroscience
Aug 12, 2009 |
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New research with transgenic mice reveals that a therapy directed at the muscle significantly improves disease symptoms of a genetic disorder characterized by destruction of the neurons that control movement. The study, published ...
Researchers find possible treatment for spinal muscular atrophy
Jul 27, 2009 |
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Spinal Muscular Atrophy is the second-leading cause of infant mortality in the world.
Researchers discover target that could ease spinal muscular atrophy symptoms
Jan 07, 2009 |
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is no cure for spinal muscular atrophy (SMA), a genetic disorder that causes the weakening of muscles and is the leading genetic cause of infant death, but University of Missouri researchers have discovered a new therapeutic ...
A natural hormone may protect muscle from atrophy
Jun 11, 2009 |
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Researchers have found a potential new treatment for the common problem of muscle atrophy.
Rare window on spinal muscular atrophy genetics
Apr 07, 2009 |
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Caused by a mutation of the SMN gene, spinal muscular atrophy (SMA) is an infantile and juvenile neurodegenerative disorder where motor neuron loss causes progressive paralysis. A new study published in the open access journal ...
Molecular Therapy for Spinal Muscular Atrophy Closer to Clinical Use
Dec 15, 2008 |
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(PhysOrg.com) -- Spinal muscular atrophy, a neurodegenerative disorder that causes the weakening of muscles, is the leading cause of infant death and occurs in 1 in 6,000 live births. While trans-splicing (a form of molecular ...
Genetic test for spinal muscular atrophy should be offered to all couples, says the ACMG
Dec 09, 2008 |
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Carrier screening for spinal muscular atrophy (SMA)—a serious genetic disease affecting approximately 1 in 10,000 infants that causes progressive muscle weakness and death—should be made available to all families, according ...
