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A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children.
Friedrich, Ulrike A; Bienias, Marc; Zinke, Claudia; Prazenicova, Maria; Lohse, Judith; Jahn, Arne; Menzel, Maria; Langanke, Jonas; Walter, Carolin; Wagener, Rabea; Brozou, Triantafyllia; Varghese, Julian; Dugas, Martin; Erlacher, Miriam; Schröck, Evelin; Suttorp, Meinolf; Borkhardt, Arndt; Hauer, Julia; Auer, Franziska.
Afiliação
  • Friedrich UA; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany; DRESDEN-concept Genome Center, Technology Platform at the Center for Molecular and Cellular Bioengineering (CMCB), Technical University of Dresden, D
  • Bienias M; Technical University of Munich, Germany, School of Medicine, Department of Pediatrics, Munich, Germany.
  • Zinke C; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Prazenicova M; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Lohse J; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Jahn A; Institute for Clinical Genetics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany; ERN GENTURIS, Hereditary Cancer Syndrome Center Dresden, Dresden, Germany; National Center for Tumor Diseases Dresden (NCT/UCC), Germany; German Cancer Research Center (DKFZ), H
  • Menzel M; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Langanke J; Pediatric Hematology and Oncology, Department of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Walter C; Institute of Medical Informatics, University of Muenster, Muenster, Germany.
  • Wagener R; Department of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine University Duesseldorf, Medical Faculty, Duesseldorf, Germany.
  • Brozou T; Department of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine University Duesseldorf, Medical Faculty, Duesseldorf, Germany.
  • Varghese J; Institute of Medical Informatics, University of Muenster, Muenster, Germany.
  • Dugas M; Institute of Medical Informatics, University of Muenster, Muenster, Germany; Institute of Medical Informatics, Heidelberg University Hospital, Heidelberg, Germany.
  • Erlacher M; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Germany.
  • Schröck E; Institute for Clinical Genetics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany; ERN GENTURIS, Hereditary Cancer Syndrome Center Dresden, Dresden, Germany; National Center for Tumor Diseases Dresden (NCT/UCC), Germany; German Cancer Research Center (DKFZ), H
  • Suttorp M; Pediatric Hematology and Oncology, Faculty of Medicine Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
  • Borkhardt A; Department of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine University Duesseldorf, Medical Faculty, Duesseldorf, Germany.
  • Hauer J; Technical University of Munich, Germany, School of Medicine, Department of Pediatrics, Munich, Germany. Electronic address: julia.hauer@mri.tum.de.
  • Auer F; Technical University of Munich, Germany, School of Medicine, Department of Pediatrics, Munich, Germany. Electronic address: f.auer@tum.de.
Genet Med ; 25(8): 100875, 2023 08.
Article em En | MEDLINE | ID: mdl-37149759
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article