63本のエピソード

A podcast about how doctors think. Presented by Figure 1, the knowledge-sharing and collaboration app for physicians and healthcare professionals. Learn more at Figure1.com/ddx

DDx Figure 1

    • 健康/フィットネス

A podcast about how doctors think. Presented by Figure 1, the knowledge-sharing and collaboration app for physicians and healthcare professionals. Learn more at Figure1.com/ddx

    Giving New Life Through X-linked Hypophosphatemia Research

    Giving New Life Through X-linked Hypophosphatemia Research

    After a lifetime of treating her rare bone disease, X-linked hypophosphatemia, a patient is at the end of her rope. She’s in pain, frustrated, and nothing seems to help. So when a clinical trial presents itself, her doctor isn’t sure she’ll want to participate. While the decision to participate is surprising, the results of the clinical trial are astonishing.

    • 10分
    The Bumpy Road to Hypoparathyroidism Diagnosis and Treatment

    The Bumpy Road to Hypoparathyroidism Diagnosis and Treatment

    A 45-year-old is out for a drive. As she accelerates her stick-shift car, she starts to experience familiar, and scary, symptoms: facial tingling, numbness around her mouth, and her hands cramp and lock onto the steering wheel … Her story takes many wrong turns, but eventually she is diagnosed with hypoparathyroidism, a rare bone disease, and finds an experimental treatment that changes her life.

    • 11分
    Unexpected Therapies for Fibrodysplasia Ossificans Progressiva Offer New Hope

    Unexpected Therapies for Fibrodysplasia Ossificans Progressiva Offer New Hope

    A 9-year-old cannonballs into the shallow end of the pool. There’s a stab of pain through her hip. What seems like just a bump takes a complicated turn. After discovering a bone growth, the child is diagnosed with fibrodysplasia ossificans progressiva. This extremely rare bone disorder has a devastating impact, but thanks to unexpected areas of research, patients have new reasons to hope.

    • 10分
    Overcoming the Odds of Prenatal Hypophosphatasia

    Overcoming the Odds of Prenatal Hypophosphatasia

    During a 20-week ultrasound appointment, there’s devastating news: the baby’s bones are broken and bowed. Despite this, the baby is born and does well. After testing, all signs point to hypophosphatasia. And thanks to the life-changing treatment of enzyme replacement therapy, today, this child and many others with this rare bone disease are living happy, healthy lives.

    • 10分
    The Power and Potential of GACI Clinical Trials

    The Power and Potential of GACI Clinical Trials

    What’s thought to be a case of newborn hiccups unravels to a grim diagnosis: generalized arterial calcification of infancy, or GACI, a rare genetic condition with a challenging prognosis. Nearly half of infants don't survive beyond six months. But a revolutionary clinical trial could potentially transform this child's life and the lives of others with this disease.

    • 9分
    Biosimilars and the Quiet Revolution in Medicine

    Biosimilars and the Quiet Revolution in Medicine

    A 62-year-old falls and fractures her wrist. This simple fracture reveals underlying osteoporosis, requiring lifelong (and expensive) medication. But this is where biosimilars come in. Biosimilars are extremely similar to the original drug they're designed to imitate, but much cheaper. This makes them more accessible to more people, meaning fewer fractures … better health … a better economy … and ultimately, a better quality of life.

    • 10分

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