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Now smartphones can diagnose Parkinson's by recording a person's voice and movements

Posted: Published on September 8th, 2014

Experts at Aston University said the 'pocket doctor' makes it possible to use voice recordings to spot the disease with 99 per cent accuracy Telltale signs include soft, breathy speech and a tremor to the voice The idea was unveiled at the British Science Festival in Birmingham Scientists said a person only has to walk for 20 paces with the phone in their pocket to get 'very high accuracy' in diagnosis By Fiona Macrae for the Daily Mail Published: 11:10 EST, 8 September 2014 | Updated: 11:12 EST, 8 September 2014 Smartphones are being turned into pocket doctors capable of spotting Parkinsons disease. The popular devices come equipped with technology needed to record speech and movement both of which are eroded by the condition, Britains biggest science conference heard. The information can then be analysed and, it is hoped, used to diagnose the disease earlier and more accurately. More prompt treatment should improve quality of life. A patients symptoms could also be tracked over time, revolutionising treatment by allowing doctors to adjust drug dosage as needed. A new smartphone app can help diagnose Parkinson's disease - suffered by Muhammad Ali and Michael J Fox (pictured) - by recording speech and … Continue reading

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Brain injuries no match for sPIF treatment

Posted: Published on September 8th, 2014

Researchers at Yale School of Medicine and their colleagues have uncovered a new pathway to help treat perinatal brain injuries. This research could also lead to treatments for traumatic brain injuries and neurodegenerative disorders such as Alzheimers and Parkinsons. The findings are published in the Sept. 8 issue of Proceedings of the National Academy of Science. The MicroRNA molecule let-7 is known to cause the death of neurons in the central nervous system. The research team found that a synthetic molecule derived from the embryo called PreImplantation Factor (sPIF) protects against neuronal death and brain injury by targeting let-7. We would never have connected the dots between PIF and let-7 without prior knowledge and experience on let-7 and H19, a developmentally regulated gene that is highly expressed in the developing embryo, said senior author Dr. Yingqun Huang, associate professor in the Department of Obstetrics, Gynecology & Reproductive Sciences at Yale School of Medicine. Using a rat perinatal brain injury model, Huang and the team found that sPIF rescued damaged neurons and reduced inflammation. The team performed a series of in vivo and in vitro experiments and found that sPIF helped to stop the production of let-7. We showed that sPIF … Continue reading

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Brain damage caused by severe sleep apnea is reversible

Posted: Published on September 8th, 2014

PUBLIC RELEASE DATE: 8-Sep-2014 Contact: Lynn Celmer lcelmer@aasmnet.org 630-737-9700 American Academy of Sleep Medicine http://www.twitter.com/AASMOrg DARIEN, IL A neuroimaging study is the first to show that white matter damage caused by severe obstructive sleep apnea can be reversed by continuous positive airway pressure therapy. The results underscore the importance of the "Stop the Snore" campaign of the National Healthy Sleep Awareness Project, a collaboration between the Centers for Disease Control and Prevention, American Academy of Sleep Medicine, Sleep Research Society and other partners. Results show that participants with severe, untreated sleep apnea had a significant reduction in white matter fiber integrity in multiple brain areas. This brain damage was accompanied by impairments to cognition, mood and daytime alertness. Although three months of CPAP therapy produced only limited improvements to damaged brain structures, 12 months of CPAP therapy led to an almost complete reversal of white matter abnormalities. Treatment also produced significant improvements in nearly all cognitive tests, mood, alertness and quality of life. "Structural neural injury of the brain of obstructive sleep apnea patients is reversible with effective treatment," said principal investigator and lead author Vincenza Castronovo, PhD, clinical psychologist at the Sleep Disorders Center at San Raffaele Hospital and … Continue reading

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Opexa Therapeutics to Target Rare Disease Neuromyelitis Optica (NMO) as next Development Program

Posted: Published on September 8th, 2014

Opexa initiated preclinical development activities for OPX-212, its drug development candidate for NMO, earlier this year and has achieved several regulatory and early development milestones to date. These include conducting a pre-IND meeting with the FDA and performing in-house manufacturing runs with NMO patient samples. The Company is continuing with preclinical development activities with a goal of filing an IND with the FDA by mid-2015 and then moving into clinical development with a Phase 1/2 proof-of-concept study. The Company believes OPX-212 will qualify for Orphan drug designation and plans also to apply for Fast Track designation for OPX-212. We are pleased to announce our development activities in a second indication utilizing our novel T-cell technology platform, said Neil K. Warma, President and Chief Executive Officer of Opexa. NMO is a disease with a significant unmet medical need. We believe our approach to the treatment of NMO with OPX-212 is highly differentiated as we are directly targeting the T-cell component of the disease and, therefore, addressing the root cause. We believe part of the value of our Precision ImmunotherapyTM T-cell platform comes from the ability to move relatively quickly and cost effectively into new autoimmune diseases. We do not expect our … Continue reading

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Smart phones to be used as pocket doctors to spot early signs of Parkinson's disease

Posted: Published on September 8th, 2014

Now there is an experimental "app" for diagnosing the neurological condition that affects about 127,000 people in the UK. The system involves sensing almost imperceptible effects on the voice, walking behaviour and manual dexterity that may provide an early indication of Parkinson's. Scientists are testing the app in a large group of 2,500 people with diagnosed Parkinson's, symptoms or genes known to be linked to the disease, and healthy individuals. An earlier analysis of thousands of voice recordings suggested that effects such as increased breathiness, drifting pitch, and altered vowel sounds can detect Parkinson's with 99% accuracy. Similarly, checking a person's gait with a smartphone's accelerometer - the in-built motion sensor that tells the device what way up it is - identified people with Parkinson's in 98% of cases. Smartphone information could also be used to assess symptom levels and progression in those being treated for the disease, say the scientists. Mathematician Dr Max Little, from the University of Aston, who is leading the research, said: "Not only can you predict whether someone has Parkinson's disease or not, you can actually score their symptoms on clinical scales. "This new kind of remote data analysis will help patients to monitor their … Continue reading

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In directing stem cells, study shows context matters

Posted: Published on September 8th, 2014

4 hours ago by Terry Devitt When blank slate stem cells are exposed to a soft as opposed to a hard surface on which to grow, they begin to transform themselves into neurons, the large, complex cells of the central nervous system. Absent any soluble factors to direct cell differentiation, surface matters, according to new research from the lab of University of Wisconsin-Madison chemist and biochemist Laura Kiessling. Credit: Kiessling Lab/UW-Madison Figuring out how blank slate stem cells decide which kind of cell they want to be when they grow upa muscle cell, a bone cell, a neuronhas been no small task for science. Human pluripotent stem cells, the undifferentiated cells that have the potential to become any of the 220 types of cells in the body, are influenced in the lab dish by the cocktail of chemical factors and proteins upon which they are grown and nurtured. Depending on the combination of factors used in a culture, the cells can be coaxed to become specific types of cells. Now, in a new study published today, Sept. 8, in the Proceedings of the National Academy of Sciences, a team of researchers from the University of Wisconsin-Madison has added a new … Continue reading

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American Nobel: Screen Women for Cancer-Causing Genetic Mutations

Posted: Published on September 8th, 2014

One of this year's five winners of the so-called American Nobels in medicine says every woman over the age of 30 needs to be tested for cancer-causing genetic mutations. The Albert and Mary Lasker Foundations Award for Special Achievement will go to Dr. Mary-Claire King, who correlated mutations in the BRCA1 and BRCA2 genes with breast and ovarian cancer. Current guidelines discourage testing, but King says it would cost little and identify 250,000 to 400,000 American women with the cancer-causing genetic mutations. The Lasker awards each include a $250,000 honorarium and are to be presented in New York September 19. The Journal of the American Medical Association summarized Kings proposal in an article published to coincide with the Lasker award announcements. The Lasker Award for Clinical Medical Research will be shared by Drs. Mahlon DeLong of Emory University in Atlanta and Alim Louis Benabid of Joseph Fourier University in Grenoble, France. They developed a surgical treatment for Parkinson's disease. In work that began in the late 1960s, DeLong traced Parkinson symptoms to over-activity in a specific part of the brain. Benabid, independently following up on that research, showed in 1995 that stimulating this area with a surgically implanted electrode could … Continue reading

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New knowledge of cannabis paves the way for drug development

Posted: Published on September 8th, 2014

PUBLIC RELEASE DATE: 8-Sep-2014 Contact: Rikke Byesen rb@nano.ku.dk 452-875-0413 Faculty of Science - University of Copenhagen Revolutionary nanotechnology method could help improve the development of new medicine and reduce costs. Researchers from the Nano-Science Center and the Department of Chemistry at the University of Copenhagen have developed a new screening method that makes it possible to study cell membrane proteins that bind drugs, such as cannabis and adrenaline, while reducing the consumption of precious samples by a billion times. About 40% of all medicines used today work through the so-called "G protein-coupled receptors". These receptors react to changes in the cell environment, for example, to increased amounts of chemicals like cannabis, adrenaline or the medications we take and are therefore of paramount importance to the pharmaceutical industry. "There is a lot of attention on research into "G protein-coupled receptors", because they have a key roll in recognizing and binding different substances. Our new method is of interest to the industry because it can contribute to faster and cheaper drug development", explains Professor Dimitrios Stamou, who heads the Nanomedicine research group at the Nano-Science Center, where the method has been developed. The new method is described in a publication at the … Continue reading

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Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory …

Posted: Published on September 8th, 2014

Background Duchenne muscular dystrophy is caused by dystrophin deficiency and muscle deterioration and preferentially affects boys. Antisense-oligonucleotide-induced exon skipping allows synthesis of partially functional dystrophin. We investigated the efficacy and safety of drisapersen, a 2-O-methyl-phosphorothioate antisense oligonucleotide, given for 48 weeks. We recruited 53 patients: 18 were given continuous drisapersen, 17 were given intermittent drisapersen, and 18 were given placebo (continuous and intermittent groups combined). At week 25, mean 6MWD had increased by 315 m (SE 98) from baseline for continuous drisapersen, with a mean difference in change from baseline of 3509 m (95% CI 759 to 6260; p=0014) versus placebo. We recorded no difference in 6MWD changes from baseline between intermittent drisapersen (mean change 01 [SE 103]) and placebo (mean difference 351 m [2434 to 3135]) at week 25. The most common adverse events in drisapersen-treated patients were injection-site reactions (14 patients given continuous drisapersen, 15 patients given intermittent drisapersen, and six given placebo) and renal events (13 for continuous drisapersen, 12 for intermittent drisapersen, and seven for placebo), most of which were subclinical proteinuria. None of the serious adverse events reported (one for continuous, two for intermittent, and two for placebo) resulted in withdrawal from the study. Continuous … Continue reading

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Brain injury treatment training planned – Video

Posted: Published on September 8th, 2014

Brain injury treatment training planned By: KTVF Channel 11 Fairbanks … Continue reading

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