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1دورية أكاديمية
المؤلفون: Martinez-Rios C; Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, Department of Radiology, University of Toronto, 555 University Avenue, Toronto, ON, M5G1X8, Canada. claudia.martinezrios@sickkids.ca., De Leon Benedetti LS; Department of Radiology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, 19104, USA., Tierradentro-Garcia LO; Department of Radiology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, 19104, USA., Kilicarslan OA; Medical Imaging Department, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, K1H8L1, Canada., Caro-Dominguez P; Unidad de Radiologia Pediatrica, Servicio de Radiodiagnostico, Hospital Universitario Virgen del Rocio Sevilla, Sevilla, 41013, Spain., Otero HJ; Department of Radiology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, 19104, USA.
المصدر: Pediatric radiology [Pediatr Radiol] 2024 Jun; Vol. 54 (7), pp. 1116-1127. Date of Electronic Publication: 2024 Apr 22.
نوع المنشور: Journal Article; Multicenter Study
بيانات الدورية: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0365332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1998 (Electronic) Linking ISSN: 03010449 NLM ISO Abbreviation: Pediatr Radiol Subsets: MEDLINE
مواضيع طبية MeSH: Hamartoma Syndrome, Multiple*/diagnostic imaging , Hamartoma Syndrome, Multiple*/genetics , PTEN Phosphohydrolase*/genetics, Humans ; Female ; Male ; Child ; Retrospective Studies ; Adolescent ; Cross-Sectional Studies ; Child, Preschool ; Infant ; Mutation