Explore Skeletal Muscle, Neurology, and more!

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Stelt de computer een betere diagnose dan de mens?

Read about a study examining skeletal muscle remodeling - degeneration and regeneration - in ALS and identifying potential disease biomarkers.

GSK has asked regulatory agencies in the U.S. and Europe to approve a new, injectable form of Benlysta to treat active, autoantibody-positive SLE.

Lupus Treatment, Benlysta, as Injection Requested for US, Europe

Biogen and Ionis Pharmaceuticals have recently issued an update on the clinical development of nusinersen, an antisense drug targeting SMA

Read about four potential serum biomarkers of disease progression and clinical outcomes in three types of muscular dystrophies.

Muscle Proteins May Serve as Serum Biomarkers for 3 Types of Muscular Dystrophy

Read about four potential serum biomarkers of disease progression and clinical outcomes in three types of muscular dystrophies.

Read of a study into imaging techniques to measure utrophin protein levels and muscle fiber regeneration in DMD patients that may advance a new therapy.

New Biomarkers for Utrophin Protein Levels Likely to Aid DMD Therapy Now in Clinical Testing

Read of a study into imaging techniques to measure utrophin protein levels and muscle fiber regeneration in DMD patients that may advance a new therapy.

Read more about the U.S. FDA granting Orphan Drug designation to the investigational drug risankizumab for pediatric patients with Crohn's disease.

FDA Grants AbbVie's Pediatric Crohn's Disease Therapy Orphan Drug Status

Santhera has just announced that its Omigapil has received U. FDA Fast Track Designation for the treatment of congenital muscular dystrophies (CMD)

Learn How to Become a Forensic Chemist, their Salary, Skills, Responsibilities, and Education #healthcare #medical #career #jobs #become #education #salary #skills #future #forensic #chemist

Learn How to Become a Forensic Chemist, their Salary, Skills, Responsibilities, and Education

Sarepta Appoints Interim CEO to Accelerate DMD Drug Process

Sarepta Appoints Interim CEO to Accelerate DMD Drug Process

Researchers Explore Effect of Prednisone For Rheumatoid Arthritis Biologics Treatments Rheumatoid Arthritis News

Systemic Inflammation Lowers With Decreased Muscle Function in Duchenne Muscular Dystrophy, According to Study

Systemic Inflammation Lowers With Decreased Muscle Function in Duchenne Muscular Dystrophy, According to Study

Psoriasis Revolution 7 Days - Inflammation in the Body: Its Causes and Effects - some unique and rare tips on how to treat psoriasis in as little as 7 days and achieve complete freedom from inflamed itchy skin, silvery scales

Researchers at the University of California San Diego recently published in the journal BMC Research Notes an approach to assess possible dysregulated mechanisms linked to Duchenne muscular dystrophy.

Researchers Reveal an Approach to Assess Deregulated Mechanisms in Duchenne Muscular Dystrophy

MS Resistance Traced to a Gene Variant in Colombia - Multiple Sclerosis News Today

Read about a proposal suggesting that Emery–Dreifuss muscular dystrophy would be an ideal candidate for the Precision Medicine Initiative.

Emery–Dreifuss Muscular Dystrophy Seen as Ideal Candidate for Precision Medicine Initiative

Pulmonary Hypertension Program at Orlando Health Heart Institute Receives National Accreditation - Lung Disease News

<span class="entry-title">Duchenne & Becker MD Patient-Centered Benefits and Risks Analysis Given to FDA</span><span class="entry-subtitle">PPMD action opens way for regulatory response to Phase III trial results of Santhera’s Raxone/Catena </span>

Duchenne & Becker MD Patient-Centered Benefits and Risks Analysis Given to FDA

Read more about Patient-Centered Benefits and Risks Analysis for Duchenne & Becker muscular dystrophy that was submitted to the FDA by PPMD.

Many Businesses could learn from the Justice Canada Scheduling & Payroll Fiasco.

Chronic Fatigue and Parkinson's Now Linked to Gut Bacteria

More than 1 million Americans live with Chronic Fatigue Syndrome (CFS), according to the Centers for Disease Control (CDC). CFS is.

Patients unable to breathe because of acute lung failure or an obstructed airway need another way to get oxygen to their blood -- and fast -- to avoid cardiac arrest and brain injury. Medical researchers have designed tiny, gas-filled microparticles that can be injected directly into the bloodstream to quickly oxygenate the blood.

Injecting life-saving oxygen into a vein

Gene-editing technique successfully stops progression of Duchenne muscular dystrophy in mouse model

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