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Treatment of neuroblastoma in congenital central hypoventilation syndrome with a PHOX2B polyalanine repeat expansion mutation: New twist on a neurocristopathy syndrome
Authors:Amy E. Armstrong MD  Debra E. Weese‐Mayer MD  Amir Mian MD  John M. Maris MD  Vandana Batra MD  Yasmin Gosiengfiao MD  Jennifer Reichek MD  Mary Beth Madonna MD  Jonathan W. Bush MD  Richard M. Shore MD  David O. Walterhouse MD
Affiliation:1. Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois;2. Ann & Robert H. Lurie Children's Hospital of Chicago, Center for Autonomic Medicine in Pediatrics (CAMP), Northwestern University of Feinberg School of Medicine and Stanley Manne Children's Research Institute, Chicago, Illinois;3. Department of Pediatric Hematology‐Oncology, College of Medicine, Arkansas Children's Hospital, University of Arkansas Medical Sciences, Little Rock, Arkansas;4. Division of Hematology, Oncology & Transplantation, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine and Abramson Family Center Research Institute, Philadelphia, Pennsylvania;5. Division of Hematology, Oncology & Transplantation, Robert Lurie Comprehensive Cancer Center, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois;6. Department of Pediatric Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois;7. Department of Pathology, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois;8. Department of Medical Imaging, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois
Abstract:
Keywords:chemotherapy  congenital central hypoventilation syndrome  MIBG  neuroblastoma  neurocristopathy  PHOX2B
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