المؤلفون: Vu-Han TL; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Frühwald MC; Children's Hospital Augsburg, Swabian Children's Cancer Center, Augsburg, Germany., Hasselblatt M; Institute of Neuropathology, University Hospital Münster, Muenster, Germany., Kerl K; Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany., Nagel I; Christian-Albrechts-University Kiel, Institute for Human Genetics, Kiel, Germany., Obser T; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Oyen F; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Siebert R; Christian-Albrechts-University Kiel, Institute for Human Genetics, Kiel, Germany., Schneppenheim R; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: schneppenheim@uke.de.

المصدر: Cancer genetics [Cancer Genet] 2014 Sep; Vol. 207 (9), pp. 390-7. Date of Electronic Publication: 2014 May 21.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101539150 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2210-7762 (Print) NLM ISO Abbreviation: Cancer Genet Subsets: MEDLINE

مواضيع طبية MeSH: Biomarkers, Tumor/*genetics , Brain Neoplasms/*pathology , Chromosomal Proteins, Non-Histone/*genetics , DNA-Binding Proteins/*genetics , Rhabdoid Tumor/*pathology , Teratoma/*pathology , Transcription Factors/*genetics, Adolescent ; Adult ; Base Sequence ; Brain Neoplasms/genetics ; Child ; Chromosome Breakpoints ; Chromosomes, Human, Pair 2/genetics ; DNA Mutational Analysis ; Humans ; Middle Aged ; Neoplasm, Residual/genetics ; Neoplasm, Residual/pathology ; Rhabdoid Tumor/genetics ; SMARCB1 Protein ; Sequence Analysis, DNA ; Sequence Deletion ; Teratoma/genetics ; Tissue Preservation ; Tumor Suppressor Proteins/genetics ; Young Adult

SCR Disease Name: Teratoid Tumor, Atypical

المؤلفون: Seeringer A; Swabian Children's Cancer Center, Children's Hospital Augsburg, Augsburg, Germany., Reinhard H; Department of Pediatric Oncology, Children's Hospital St. Augustin, Sankt Augustin, Germany., Hasselblatt M; Institute of Neuropathology, University Hospital Münster, Münster, Germany., Schneppenheim R; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Siebert R; Institute of Human Genetics, Christian-Albrechts-University Kiel and University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany., Bartelheim K; Swabian Children's Cancer Center, Children's Hospital Augsburg, Augsburg, Germany., Leuschner I; Institute of Pathology, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany., Frühwald MC; Swabian Children's Cancer Center, Children's Hospital Augsburg, Augsburg, Germany; Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany. Electronic address: michael.fruehwald@klinikum-augsburg.de.

المصدر: Cancer genetics [Cancer Genet] 2014 Sep; Vol. 207 (9), pp. 429-33. Date of Electronic Publication: 2014 Jul 03.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101539150 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2210-7762 (Print) NLM ISO Abbreviation: Cancer Genet Subsets: MEDLINE

مواضيع طبية MeSH: Brain Neoplasms/*congenital , Chromosomal Proteins, Non-Histone/*genetics , DNA-Binding Proteins/*genetics , Neoplasms, Multiple Primary/*genetics , Orbital Neoplasms/*congenital , Rhabdoid Tumor/*congenital , Teratoma/*congenital , Transcription Factors/*genetics, Antineoplastic Agents/therapeutic use ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Brain Neoplasms/pathology ; Brain Neoplasms/therapy ; Child, Preschool ; Chromosome Deletion ; Chromosomes, Human, Pair 22/genetics ; Combined Modality Therapy ; Female ; Humans ; Kidney Neoplasms/congenital ; Kidney Neoplasms/pathology ; Kidney Neoplasms/therapy ; Neoplasms, Multiple Primary/congenital ; Neoplasms, Multiple Primary/pathology ; Orbital Neoplasms/pathology ; Orbital Neoplasms/therapy ; Rhabdoid Tumor/pathology ; Rhabdoid Tumor/therapy ; SMARCB1 Protein ; Survivors ; Teratoma/pathology ; Teratoma/therapy

SCR Disease Name: Rhabdoid Tumor Predisposition Syndrome 1; Teratoid Tumor, Atypical