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	Profile	Recent Articles on Subject
1	Emily Cooke Live Science Health reporter. London, United Kingdom healthscience	People with this rare genetic condition can't repair damage to their DNA - 25 days ago Stone man disease: A rare condition that causes a person to grow a second skeleton - 3 months ago
2	Tara Haelle MedPage Today Sci/health journalist. Feminist. Educator. Photographer. Author. DFW science journalismhealthphotographyteaching	Children With IBD Showed Impaired Growth Before Diagnosis - about 1 month ago
3	Kristen Monaco MedPage Today	Denosumab May Offer Better Fracture Protection for Dialysis Patients - about 2 months ago Imcivree Label Expanded; Weight Loss With Weekly Injection; Kidney Donation Chain - 2 months ago Consider All Prior Fractures During Osteoporosis Assessment, Study Suggests - 3 months ago FDA Slaps Boxed Warning on Osteoporosis Drug - about 1 year ago
4	David Nield Science Alert Freelance tech, science writer. Marple, Manchester, UK Technologysciencewriting	Gene Inherited From Neanderthals Influenced The Shape of Our Teeth - about 2 months ago
5	Elise Reuter MedTech Dive Reporter @MedTechDive. Covers medical devices. medical technologydigital therapeutics	Zimmer receives FDA nod for stemless shoulder implant - 3 months ago
6	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 - 3 months ago FDA Grants Orphan Drug Designation to AISA-021 for Systemic Sclerosis - 6 months ago Study Finds Similarities Between SB16 and Denosumab for Osteoporosis Treatment Up to 18 Months - 9 months ago FDA Approves Vosoritide for Children With Achondroplasia - over 1 year ago
7	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 - 4 months ago
8	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: Perplexing results from Duchenne muscular dystrophy trial raise questions about gene therapies - 4 months ago STAT+: FDA rejects Rocket Pharmaceuticals’ gene therapy for ultra-rare condition, another setback for field - 8 months ago
9	The Conversation Science Alert Science news. Official account. Australia science news	These Tiny, Overlooked Bones Could Tell Us Why Our Knees Hurt - 6 months ago
10	Kennedy Ferruggia, Assistant Editor Pharmacy Times #pharmacy news, insights. CE provider. Cranbury, New Jersey pharmacyhealthcarejournalism	FDA Grants Rare Pediatric Disease Designation to NS-050/NCNP-03 to Treat Muscle Wasting Disease - 6 months ago FDA Grants Regenerative Medicine Advanced Therapy Designation for OBX-115 - 6 months ago Study Finds Higher Rates of Complications Following Scoliosis Surgery in Teens Due to Disparities - over 1 year ago

Journalists covering osteogenesis imperfecta