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Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasia
Authors:Cristian D. Gonzalez MD  Jamie Mcdonald MS  David A. Stevenson MD  Kevin J. Whitehead MD  Matthew G. Petersen BS  Angela P. Presson PhD  Qian Ding MSAT  Kevin F. Wilson MD
Affiliation:1. Department of Internal Medicine, University of Utah Affiliated Hospitals, Salt Lake City, Utah, U.S.A;2. Department of Pathology, University of Utah, Salt Lake City, Utah, U.S.A;3. Department of Radiology, University of Utah, Salt Lake City, Utah, U.S.A;4. Department of Pediatrics, Division of Medical Genetics, Stanford University, Stanford, California, U.S.A;5. George E. Wahlen VA Medical Center, Salt Lake City, Utah, U.S.A;6. University of Utah School of Medicine, Salt Lake City, Utah, U.S.A;7. Division of Epidemiology, Salt Lake City, Utah, U.S.A;8. Division of Otolaryngology–Head and Neck Surgery, University of Utah, Salt Lake City, Utah, U.S.A;9. Division of Cardiovascular Medicine, Pediatric Cardiology, Molecular Medicine Program, University of Utah, Salt Lake City, Utah, U.S.A
Abstract:
Keywords:Genodermatoses  hereditary hemorrhagic telangiectasia  epistaxis  pediatrics
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