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Researcher Spotlights – January 2022
… School of Medicine in Durham, North Carolina. He then completed a plastic surgery training at the University of … He is currently the principal investigator for a 14-site NIH-funded study of comparative effectiveness of … work, Dr. Walsh is dedicated to research and mentoring future generations of physicians specializing in …
Condition
Hereditary Hemochromatosis What is hereditary hemochromatosis? Hereditary hemochromatosis is a genetic blood disorder that causes your body to absorb too much iron from the food you eat. Iron is a mineral found in many foods. But too much iron is toxic to your body. The excess
Condition
Facioscapulohumeral Muscular Dystrophy in Children What is FSHD in children? Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs. These muscles weaken and shrink
Doctor
Neil R. Friedman, MBChB
Director, Clinical Transformation; Diane and Bruce Halle Endowed Chair in Pediatric Neurosciences
Specialties
Condition
Tracheoesophageal Fistula and Esophageal Atresia What are tracheoesophageal fistula and esophageal atresia? Tracheoesophageal fistula Tracheoesophageal fistula is a connection between the esophagus and the trachea. The esophagus is the tube that connects the throat to the stomach
Curricula & Schedules
The Pediatric Rheumatology Fellowship Training Program at Phoenix Children's is a comprehensive 36-month ACGME-accredited program focused on providing fellows with the necessary skills and knowledge to offer optimal care for pediatric patients with rheumatic diseases. The program
Condition
Nosebleed (Epistaxis) in Children What is a nosebleed in children? A nosebleed is bleeding from tissues inside the nose (nasal mucus membranes) caused by a broken blood vessel. The medical word for nosebleed is epistaxis. Most nosebleeds in children occur in the front (anterior)
Condition
Osteogenesis Imperfecta in Children What is osteogenesis imperfecta in children? Osteogenesis imperfecta (OI) is a rare inherited (genetic) bone disorder that is present at birth. It's also known as brittle bone disease. A child born with OI may have soft bones that break
Service,
Specialty
The pediatric experts at Phoenix Children’s Primary & Complex Care provide coordinated, compassionate care for children with a wide range of medical needs. From routine checkups, preventive care and vaccines to treatment for illnesses and coordinated management for complex