Sentences with phrase «muscle disease»

A man offers $ 100,000, his house, and all his possessions to save his wife from dying of a degenerative muscle disease.
A chemical found in plants could reduce the symptoms of a rare muscle disease that leaves children with little or no control of their movements.
If I raise my bail by then, I can go free and help a kid with muscle disease.
For decades, researchers have struggled to find suitable treatments for genetic muscle diseases like this one.
Some are prone to eye problems, ear infections because of their floppy ears, and a few lines have inherited muscle diseases.
The hospital told her parents she must have a rare muscle disease.
Scientists at Icahn School of Medicine at Mount Sinai, along with collaborators at institutions in India, Italy, and Japan, have identified the first gene linked to childhood - onset familial dilated cardiomyopathy (DCM), one of the most common heart muscle diseases in children.
The most common heart disease in cats, hypertrophic cardiomyopathy (HCM) is a heart muscle disease in which the walls of the heart, specifically the left ventricle, become abnormally thickened.
She completed a PhD involving the study of muscle disease in horses; with focus on polysaccharide storage myopathy in 2005.
The findings are a major step towards developing a stem cell replacement therapy for muscle diseases including Duchenne Muscular Dystrophy, which affects approximately 1 in 5,000 boys in the U.S. and is the most common fatal childhood genetic disease.
When parents of children suffering from muscle diseases contact Dr. Daniel MacArthur's lab, it's often after they've exhausted their options.
Members of the section are collaborating with investigators from the National Center for Advancing Translational Sciences (NCATS) to treat a late - onset muscle disease called GNE myopathy using sialic acid, whose production is defective in that disorder.
Researchers present the first clinical study that provides evidence that an extended - release sialic acid supplement may stabilize muscle strength in patients with GNE myopathy (GNEM), a rare hereditary, progressive, adult - onset muscle disease.
The research opens the door for new approaches to treat muscle diseases including muscular dystrophies, which affect approximately 50,000 people in the U.S., and muscle wasting associated with cancer and aging.
«Phase 2 clinical trial to treat rare hereditary muscle disease shows promise: Loss of muscle strength slowed with extended - release drug, according to report.»
HCM is a primary heart muscle disease where the muscular walls of the ventricles become abnormally thickened (hypertrophied.)
She has a particular interest and expertise in skeletal muscle disease, epigenetics and growth factor signalling.
Includes worming and boosters for vitamin E and selenium to prevent white muscle disease.
Young Americans living with a devastating muscle disease in the U.S. face an approximately $ 88,000 price hike for a year's worth of treatment that's been around for decades.
After college he worked at Massachusetts General Hospital in a laboratory studying muscle diseases.
While transplantation of such muscle stem cells can be a potent therapy for degenerative muscle diseases such as Duchenne muscular dystrophy, these cells tend to lose their transplantation efficiency when cultured in vitro.
«We report here a gene therapy dose - finding study in a large animal model of a severe muscle disease where a single treatment resulted in dramatic rescue,» said Childers.
The discovery of the gene for Native American myopathy, however, may help develop drugs to treat the myopathy, as well as other related muscle diseases.
Valve disease is prevalent in smaller breeds like the Cavalier King Charles Spaniel while muscle diseases like cardiomyopathy are prevalent in larger breeds like the Doberman Pinscher.
Two weeks later, the researchers found the brain - derived cells in the regenerating muscle tissue — suggesting that neural stem cell lines might be candidates for treating certain muscle diseases.
Dr. Jamel Chelly, Institut Cochin, Université Paris - Descartes, CNRS (UMR 8104), Paris, France, (Human muscle diseases and cell banking)
This in turn will allow developing the tools and concepts to utilize cell fusion as a mean to repair ailing muscles in heritable muscle diseases (myopathies).
Studies the genetics of degenerative muscle diseases using mouse models for SMA, ALS, muscular dystrophy and more.
Dr. Firshman's research interests focus on muscle diseases and endocrine disorders.
Dogs with substantial concomitant muscle disease (DM & DM - like) may have difficulties in prehension and swallowing.
Concurrent clinical, electromyographic, or histologic evidence of muscle disease aids in diagnosis.
This is a degenerative muscle disease first characterized in the Labrador Retriever.
Some dogs are born with cardiac muscle diseases, and are genetically prone to certain cardiac and / or whole circulatory system problems.
Introduction to Doberman Pinscher Five Gifts Prong Collar revisited Behavioral Bend Bloat Dogs & Cats Heart Muscle Disease Lumps and Bumps Multi dog households Thyroid Gland Disease Wobbler Syndrome Von Williebrand Disease
Restrictive cardiomyopathy, which accounts for approximately 10 percent of the primary heart muscle diseases diagnosed in Dr. Bonagura's practice, is caused by the excessive buildup of scar tissue on the inner lining and muscle of a ventricle.
Unfortunately, every character in the game not being actively controlled by the player suffers some sort of debilitating muscle disease, as they are completely helpless, and constantly require you to stop what you're doing and run over to help them.
Samsung notes that wearable robot suits could have various purposes, such as for helping movements of disabled persons, the elderly, and the infirm by assisting their muscle strengths when they move, for rehabilitation treatment for muscle disease patients, for soldiers who carry heavy military gears, or for industrial sites in which workers carry heavy loads have been briskly developed.
The study, published September 7 in Nature Medicine, provides promise for a new therapeutic approach to treating the millions of people suffering from muscle diseases, including those with muscular dystrophies and muscle wasting associated with cancer and aging.
An example would be muscular dystrophy, which is a devastating genetic muscle disease.
«First gene linked to heart muscle disease in children found.»
Zebrafish with very weak muscles helped scientists decode the elusive genetic mutation responsible for Native American myopathy, a rare, hereditary muscle disease that afflicts Native Americans in North Carolina.
This skeletal muscle disease is characterized by stiff muscles and a weakness that limits activity as it worsens.
Similar to «white muscle disease» in cattle, Keshan disease caused the heart muscle to degenerate.
In addition, ERA Real Solutions Realty regularly gives back to the community, most recently as a proud supporter of ERA's MDA Summer Camp Challenge, which rallied ERA companies across the country to send 1,000 children with muscle disease to barrier - free summer camp over a three - year period.
The ability to start from cellular scratch using non-muscle tissue will allow scientists to grow far more muscle cells, provide an easier path to genome editing and cellular therapies, and develop individually tailored models of rare muscle diseases for drug discovery and basic biology studies.
We're excited about the implications of our research for treating muscle diseases, and look forward to applying our conclusions toward development of therapies.»
«New advances in medication for muscle disease in children.»
This latter point will permit a more in - depth analysis of MuSC biology, genetic modification / correction of MuSCs, drug screenings, and, importantly, the development of new and improved MuSC - based therapies for a wide range of muscle diseases.
We are also studying mice with degenerative muscle diseases that are models for specific forms of muscular dystrophy in humans.
Canine Phosphofructokinase (PFK) deficiency is an autosomal recessive genetic disease which prevents the metabolism of glucose into available energy resulting in exercise intolerance and muscle disease in Cocker Spaniels.
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