Uwe Kordes

Summary

Affiliation: University Medical Center Hamburg-Eppendorf
Country: Germany

Publications

  1. doi request reprint Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany
    Genes Chromosomes Cancer 49:176-81. 2010
  2. doi request reprint Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany
    Pediatr Blood Cancer 54:758-60. 2010
  3. pmc Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome
    Reinhard Schneppenheim
    Department of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Martinistrasse 52, Hamburg, Germany
    Am J Hum Genet 86:279-84. 2010
  4. ncbi request reprint Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS)
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany
    Pediatr Blood Cancer 61:919-21. 2014
  5. doi request reprint Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression
    Christian Hagel
    Institute of Neuropathology, University Medical Center Hamburg Eppendorf, Martinistr 52, 20246, Hamburg, Germany
    J Neurooncol 112:191-7. 2013
  6. ncbi request reprint Sox group E gene expression distinguishes different types and maturational stages of glial cells in developing chick and mouse
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Hospital Hamburg Eppendorf, Martinistr 52, 20246 Hamburg, Germany
    Brain Res Dev Brain Res 157:209-13. 2005

Collaborators

Detail Information

Publications6

  1. doi request reprint Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany
    Genes Chromosomes Cancer 49:176-81. 2010
    ..001). Patients with germline mutation of SMARCB1 manifest at an early age and have a very high risk for progression which has to be considered with respect to the outcome of further treatment studies...
  2. doi request reprint Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany
    Pediatr Blood Cancer 54:758-60. 2010
    ..A detailed work-up failed to reveal other specific factors contributing to cholestasis. Severe hemolytic disease of the newborn may cause cholestasis even in the absence of associated primary hepato-biliary disease...
  3. pmc Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome
    Reinhard Schneppenheim
    Department of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Martinistrasse 52, Hamburg, Germany
    Am J Hum Genet 86:279-84. 2010
    ..SMARCA4 is thus a second member of the SWI/SNF complex involved in cancer predisposition. Its general involvement in other tumor entities remains to be established...
  4. ncbi request reprint Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS)
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany
    Pediatr Blood Cancer 61:919-21. 2014
    ..In conclusion, intensive treatment with curative intent is justified for children with rhabdoid tumors even if an underlying rhabdoid predisposition syndrome is demonstrated...
  5. doi request reprint Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression
    Christian Hagel
    Institute of Neuropathology, University Medical Center Hamburg Eppendorf, Martinistr 52, 20246, Hamburg, Germany
    J Neurooncol 112:191-7. 2013
    ..However, because of the small sample size the results are of preliminary nature and replication in a larger cohort would be desirable...
  6. ncbi request reprint Sox group E gene expression distinguishes different types and maturational stages of glial cells in developing chick and mouse
    Uwe Kordes
    Department of Pediatric Hematology and Oncology, University Hospital Hamburg Eppendorf, Martinistr 52, 20246 Hamburg, Germany
    Brain Res Dev Brain Res 157:209-13. 2005
    ..Sox8 appeared both in oligodendrocytes and astrocytes, Sox9 was more abundant in astrocytes and Sox10 was restricted to later stages of oligodendrocyte development...