Find and Pitch Jounalists, Get Your Story Covered

Tags: muscular dystrophy duchenne muscular dystrophy PTC fat weight gain

	Profile	Recent Articles on Subject
1	Kennedy Ferruggia, Assistant Editor Pharmacy Times #pharmacy news, insights. CE provider. Cranbury, New Jersey pharmacyhealthcarejournalism	FDA Grants Priory Review for Human Monoclonal Antibody Drug to Treat Muscle-Invasive Bladder Cancer - 20 days ago FDA Grants Rare Pediatric Disease Designation to NS-050/NCNP-03 to Treat Muscle Wasting Disease - 4 months ago FDA Grants Rare Pediatric Disease Designation to SAT-3247 to Treat Duchenne Muscular Dystrophy - 5 months ago
2	Emily Cooke Live Science Health reporter. London, United Kingdom healthscience	Stone man disease: A rare condition that causes a person to grow a second skeleton - 28 days ago New mRNA therapy shows promise in treating 'ultrarare' inherited disease - 9 months ago
3	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: Novartis buys gene therapy startup Kate Therapeutics, joining pursuit of muscular dystrophy treatment - about 1 month ago STAT+: Perplexing results from Duchenne muscular dystrophy trial raise questions about gene therapies - 2 months ago STAT+: Pfizer’s gene therapy for Duchenne muscular dystrophy fails in Phase 3 trial - 7 months ago STAT+: Avidity Biosciences says its experimental drug showed potential against form of muscular dystrophy - 7 months ago STAT+: Duchenne muscular dystrophy drug from Nippon Shinyaku fails in rare confirmatory trial - 7 months ago STAT+: FDA approves first gene therapy for fatal neuron disease in children - 9 months ago STAT+: Sarepta’s Duchenne gene therapy fails to meet primary endpoint in pivotal trial - about 1 year ago STAT+: What to know about Sarepta’s upcoming data on its Duchenne gene therapy - about 1 year ago
4	Greg Laub MedPage Today Director of Video at MedPage Today. Screenwriter, previous managing editor. videographyscreenwritingediting	Myasthenia Gravis: Balancing Traditional Immunotherapies vs Newer Medications - about 1 month ago Inebilizumab for Myasthenia Gravis Reduces Steroid Burden - about 2 months ago Multiple Sclerosis: Treat Early With High-Efficacy Therapy - about 1 year ago Multiple Sclerosis: Paving the Way to a Cure - about 1 year ago MS Treatment-Discontinuation Study Terminated After Disease Activity Returns - about 1 year ago
5	Ashley Gallagher, Associate Editor Pharmacy Times One of Cabra girls on GoggleboxIRL. Dublin City, Ireland televisionentertainment	FDA Grants Rare Pediatric Disease Designation for Treatment of Neonatal SP-B Deficiency - about 1 month ago FDA Grants Orphan Drug Designation to RAG-18 for Duchenne, Becker Muscular Dystrophy - 4 months ago FDA Approves Givinostat as First Nonsteroidal Drug for Duchenne Muscular Dystrophy - 9 months ago
6	Kristen Monaco MedPage Today	Year in Review: Tardive Dyskinesia - about 2 months ago Assessing Tardive Dyskinesia Risk - 4 months ago ADHD and Dementia; Alleged Sex Assault in MDMA Trial; iPhones Screen for Depression - about 1 year ago
7	STAT Staff STAT News Frontiers of health & medicine reporting. healthmedicinejournalism	The biotech updates you need to read this morning - 2 months ago
8	Adam Feuerstein STAT News Reporter at STATnews. Dog lover. Polk Award winner. Boston, Massachusetts biotech reporting	STAT+: Perplexing results from Duchenne muscular dystrophy trial raise questions about gene therapies - 2 months ago STAT+: Sarepta’s Duchenne gene therapy fails to meet primary endpoint in pivotal trial - about 1 year ago
9	John Gever MedPage Today MedPage Today factotum. Pittsburgh, Pa. Healthcare journalism	Study Offers Clues for Avoiding RMD Flares After COVID Vaccination - 2 months ago
10	Sophie Putka MedPage Today Enterprise, investigative writer. New York, USA enterprise journalisminvestigative journalism	A Miss for Steroid-Toting Red Blood Cells in Ataxia Telangiectasia - 4 months ago Givinostat Slows Duchenne Muscular Dystrophy Decline - 9 months ago Obesity Associated With Faster MS Disease Progression - 10 months ago No Change in Huntington's Motor Symptoms With Investigational Drug - 11 months ago

Journalists covering muscular dystrophy