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  1. Cirugía - Ensayos clínicos - Mayo Clinic

    The purpose of this study is to assess the differences in microvascular anastomosis outcomes between the experiment aneurysmal subarachnoid hemorrhage (aSAH)- ...

  2. Cirugía - Ensayos clínicos - Mayo Clinic

    This randomized phase II/III trial studies how well radiation therapy works when given together with cisplatin compared to docetaxel or cetuximab and ...

  3. Diagnósticos y tratamientos - Mayo Clinic

    Hepatic encephalopathy is diagnosed by looking at the medical history, signs and symptoms, medicine use, and the results of blood tests and other tests. Tests ...

  4. Bardet-Biedl syndrome (BBS)

    Bardet-Biedl (BAR-day, BEE-dul) syndrome, also called BBS, is a rare condition caused by changes in genes. BBS can affect almost any part of the body. Starting ...

  5. Diagnósticos y tratamientos - Mayo Clinic

    To diagnose adnexal tumors and masses, a healthcare professional may start with a pelvic exam. Other tests and procedures might include imaging tests and blood ...

  6. Deficiencia de alfa-1 antitripsina - Síntomas y causas - Mayo Clinic

    Alpha-1-antitrypsin deficiency (AATD) is a condition that's passed through families, called inherited. It can cause damage to the lungs, liver, skin and blood ...

  7. Oncología (médica) - Ensayos clínicos - Mayo Clinic

    This trial studies how well two surgical procedures (bilateral salpingectomy and bilateral salpingo-oophorectomy) work in reducing the risk of ovarian cancer ...

  8. Síntomas y causas - Mayo Clinic

    Descripción general. Diffuse midline glioma (DMG) is a rare type of cancerous brain tumor. It's most common in children between the ages of 5 and 10 years ...

  9. Obstetricia y Ginecología - Ensayos clínicos - Mayo Clinic

    The postnatal diagnosis of Long QT Syndrome (LQTS) is suggested by a prolonged QT interval on 12 lead electrocardiogram (ECG),a positive family history ...

  10. Plexiform neurofibroma - Diagnósticos y tratamientos - Mayo Clinic

    Explore how plexiform neurofibromas are diagnosed and treated using advanced imaging, genetic testing, and a range of medical and surgical options.