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1761-1770 of 2600 Results Found
Alumni
Our graduates have gone on to fellowships at: Children’s Hospital of Orange County Stanford University Pediatric Endocrinology University of Texas Health Science Center Cincinnati Children’s Hospital & Medical Center Children’s Hospital Colorado Children’s Hospital of
CME Session
PCH - Newborn screening and Inborn Errors in Metabolism - Dr. Shagun Kaur
Overall Activity Objectives: Implement appropriate strategies for diagnosing pediatric conditions. Evaluate and implement appropriate, current treatment options vis a vis emerging therapeutics. Implement in practice developing areas of research and evidence-based recommendations
Patient Family Experience Award
Everyone at Phoenix Children’s has an impact on the patient family experience. From clinicians to volunteers and guest services to contract staff, we want to recognize those who go the extra mile to improve a patient family’s experience. Are you a Phoenix Children’s patient
Doctor
Christina L. Garry, PNP
Specialties
  • Hematology & Oncology
Christina L. Garry, PNP
CME Session
Diagnosis and Management of Osteogenesis Imperfecta
Presenting live from Cohen Conference Center or via Live Stream Presenters: Rachel C. Lombardo, MD (left) Pediatrician, Genetics and Metabolism, Phoenix Children's Pamela Smith, MD (center) Medical Director, Metabolic Bone & Osteogenesis Imperfecta (OI) Clinic, Phoenix Children's
Doctor
Jennifer S. Ronecker, MD
Associate Program Director, Neurosurgery
4.8 / 5
Specialties
  • Neurosurgery
Jennifer S. Ronecker, MD
Service
Voiding Improvement Clinic
The Voiding Improvement Clinic is the first voiding dysfunction clinic in Arizona, directed by pediatric urologists. Our goal is to provide the highest quality pediatric urological care to our patients in an environment that feels secure and comforting to children, their families
Doctor
Mohammed Elkhwad, MD
Specialties
  • Neonatology
Mohammed  Elkhwad, MD
Curriculum
The Medical Genetics and Genomics Residency Program is a two-year residency program providing rotations in inpatient Genetics, cytogenetics, biochemical/molecular, and molecular genetics lab, prenatal, adult genetics, as well as dedicated blocks for research. MGG continuity
CME Session
PCH - Sudden Infant Death Syndrome: Research and Risk Reduction - Dr. Thomas Keens, Children's Hospital of Los Angeles
Guest Presenter: Thomas Keens, MD, Director, Cystic Fibrosis Center, Attending Physician, Professor of Pediatrics, Physiology and Biophysics, Keck School of Medicine of USC, Children's Hospital Los Angeles Clinical Interests Cystic fibrosis, Sudden infant death syndrome

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