Spinal Muscular Atrophy Current Events | Spinal Muscular Atrophy News | 2
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Media Invite: Spinal Research Centre Open Day 7th July
Director of the Spinal Research Centre, Professor Michael Craggs, is hosting an open day of the Spinal Research Centre at the Royal National Orthopaedic Hospital, Stanmore. The research strategy of the SRC is based upon a number of key research programmes, which cover all aspects of the needs of patients with dysfunction of the spine or spinal... view more... (2004-07-05)
Media invitation: Groundbreaking spinal injury therapy to be showcased in new exhibition
In response to a recent study published by a team of doctors from Imperial College London and Charing Cross hospital, the Science Museum in London has created a mini exhibition exploring magnetic therapy. The recent study found early evidence that administration of magnetic stimulation to the brains of people with incomplete lesions of the spinal... view more... (2004-05-20)
New therapeutic insight into duchenne muscular dystrophy
In the April 1st issue of Genes & Development, Dr. Bruce Spiegelman (Dana Farber Cancer Institute) and colleagues identify a key genetic component of and possible therapeutic target for Duchenne muscular dystrophy. view more (2007-04-02)
Neurons grown from embryonic stem cells restore function in paralyzed rats
For the first time, researchers have enticed transplants of embryonic stem cell-derived motor neurons in the spinal cord to connect with muscles and partially restore function in paralyzed animals. view more (2006-06-21)
Long-term use of mechanical ventilation contributes to the deterioration of human diaphragm muscle
A new study by University of Pennsylvania School of Medicine shows, for the first time in humans, that ventilators combined with diaphragm disuse contributes to muscle atrophy in the diaphragm in as little as eighteen hours. view more (2008-03-27)
Researchers identify gene associated with muscular dystrophy-related vision problems
Skeletal muscle disease and vision deficits might seem unrelated, but a frog model of muscular dystrophy shows it is not such a leap. view more (2009-04-21)
Gene therapy for muscular dystrophy shows promise beyond safety
Researchers have cleared a safety hurdle in efforts to develop a gene therapy for a form of muscular dystrophy that disables patients by gradually weakening muscles near the hips and shoulders. view more (2009-04-16)
Human stem cell transplants mature into neurons and make contacts in rat spinal cord
Human nerve stem cells transplanted into rats' damaged spinal cords have survived, grown and in some cases connected with the rats' own spinal cord cells in a Johns Hopkins laboratory, overturning the long-held notion that spinal cords won't allow nerve repair. view more (2007-02-14)
Potential therapy for congenital muscular dystrophy
Current research suggests laminin, a protein that helps cells stick together, may lead to enhanced muscle repair in muscular dystrophy. view more (2008-12-30)
Electric Therapy helps Muscle Spasticity
Researchers in Austria who have been trying to overcome spasticity in people with spinal cord injury have made significant progress that might, in the future, help patients to stand. A technique called spinal cord stimulation is showing promise for people whose legs are bent and stiffened due to damaged nerves as a result of injury. Dr Michaela... view more... (2002-10-24)
Mimicking a human disease in mice: a new model for the Parkinson related illness multiple system atrophy
In this month`s issue of EMBO Reports Kahle et al. describe how they genetically engineered a mouse to show pathological symptoms similar to those of human patients suffering from the neural disease Multiple System Atrophy (MSA), also known as Shy-Drager-Syndrome. The model could help researchers to develop and test new efficient drugs against... view more... (2002-06-06)
MRI shows brain atrophy pattern that predicts Alzheimer's
Using special MRI methods, researchers have identified a pattern of regional brain atrophy in patients with mild cognitive impairment (MCI) that indicates a greater likelihood of progression to Alzheimer's disease. The findings are published in the online edition of Radiology. view more (2009-02-10)
Researchers discover treatment for spinal cord injury pain
Spinal cord injury patients with moderate to severe nerve pain experienced less pain and in some cases no pain while taking the drug pregabalin. view more (2006-11-28)
Stem cells - a cure for fatal muscular dystrophy
The diagnosis 'muscular dystrophy' is usually tantamount to a death sentence for those affected. One in three thousand male babies suffer from this incurable hereditary disease. The progress of the disease can only be slowed down through physiotherapy and medication. Scientists at Bonn University and at Pittsburgh Children's Hospital (USA) have... view more... (2002-07-04)
Researchers identify new function for protein missing in Duchenne muscular dystrophy
Researchers at the University of Minnesota and National Institutes of Health have identified a new function for the protein missing in people with the most common and ultimately lethal form of childhood muscular dystrophy. view more (2009-08-04)
Purdue researchers find 'switch' for skeletal-muscle atrophy
Researchers in Purdue University's School of Veterinary Medicine have discovered genetic and drug-treatment methods to arrest the type of muscle atrophy often caused by muscle disuse, as well as aging and diseases such as cancer. view more (2006-05-25)
Lamin A/C deficiency is 'unnerving'
Mutations in the nuclear intermediate filament lamin A/C (LMNA) gene are associated with Emery-Dreifuss muscular dystrophy, but cause the disease by unknown mechanisms. Méjat et al. show that one mechanism involves the disruption of neuromuscular junctions. view more (2009-01-05)
Muscle atrophy through thick but not thin
During desperate times, such as fasting, or muscle wasting that afflicts cancer or AIDS patients, the body cannibalizes itself, atrophying and breaking down skeletal muscle proteins to liberate amino acids. view more (2009-06-08)
MRC Research Offers Hope of Treatment for People with Duchenne Muscular Dystrophy
A new approach which effectively patches over genetic defects offers hope of treatment to people with the terminal illness, Duchenne muscular dystrophy. This is the conclusion of research led by Dr Qi Long Lu and Professor Terence Partridge at the Medical Research Council's Clinical Sciences Centre. Most cases of Duchenne muscular dystrophy are... view more... (2003-07-04)
Researchers make progress toward early identification of muscular dystrophy
The saying "Knowing is half the battle" is never more true than when discussing early treatment of disease. Muscular dystrophy is one such disease where patients can benefit from early treatment. Now, new research is moving doctors and scientists closer to disease diagnosis in advance of patient symptoms. view more (2009-06-17)
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