Friederike Körber

Summary

Affiliation: University of Cologne
Country: Germany

Publications

  1. ncbi request reprint [Sonography of the optical nerve -- experience in 483 children]
    F Korber
    Kinderradiologie, Justus Liebig Universitat Giessen
    Rofo 177:229-35. 2005
  2. pmc The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
    Ghada Abdel-Salam
    Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany
    Orphanet J Rare Dis 9:12. 2014
  3. ncbi request reprint Introduction of a new standardized assessment score of spine morphology in osteogenesis imperfecta
    F Koerber
    Department of Radiology, University of Cologne
    Rofo 184:719-25. 2012
  4. ncbi request reprint Isolated femoral hypoplasia: an intrauterine differential diagnosis to campomelia
    Friederike Körber
    Department of Paediatric Radiology, University of Cologne, Joseph Stelzmann Strasse 9, Cologne, Germany
    Pediatr Radiol 35:641-6. 2005
  5. ncbi request reprint [Occlusion of the left portal vein in newborns]
    F Korber
    Institut und Poliklinik für Radiologische Diagnostik, Kinderradiologie, Uniklinik Köln
    Ultraschall Med 32:472-8. 2011
  6. ncbi request reprint [Standardized x-ray reports of the spine in osteogenesis imperfecta]
    F Koerber
    Institut und Poliklinik für Radiologische Diagnostik, Kinderradiologie, Uniklinik Köln
    Rofo 183:462-9. 2011
  7. ncbi request reprint A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
    Guntram Borck
    Institute of Human Genetics, University of Cologne, Kerpener Str 34, 50931, Cologne, Germany
    Hum Genet 129:45-50. 2011

Collaborators

  • O Semler
  • F Koerber
  • Ghada Abdel-Salam
  • S Koerber
  • E Schönau
  • Guntram Borck
  • Daniel Swan
  • Hanan H Afifi
  • Hanno Jörn Bolz
  • Michaela Thoenes
  • U Schulze Uphoff
  • D Maintz
  • Christian Kubisch
  • Bernd Wollnik
  • Deborah J Morris-Rosendahl
  • Angela Steiert
  • K J Lackner
  • Alexander E Volk
  • Peter Herkenrath
  • A W Demant
  • Heidrun Wunram
  • Sigrid Roters

Detail Information

Publications7

  1. ncbi request reprint [Sonography of the optical nerve -- experience in 483 children]
    F Korber
    Kinderradiologie, Justus Liebig Universitat Giessen
    Rofo 177:229-35. 2005
    ..The purpose of the study was to gain clinical experience in children and to determine (a) the mean values for patients without proven IICP and (b) pathologic values of those with proven IICP...
  2. pmc The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
    Ghada Abdel-Salam
    Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany
    Orphanet J Rare Dis 9:12. 2014
    ..It is therefore considered a tumor suppressor gene, but its direct implication in cancerogenesis remains controversial...
  3. ncbi request reprint Introduction of a new standardized assessment score of spine morphology in osteogenesis imperfecta
    F Koerber
    Department of Radiology, University of Cologne
    Rofo 184:719-25. 2012
    ..In this paper, radiological changes of the spine are quantified according to their clinical relevance to define a scoring system that transfers the morphological changes into a single value representing the severity of the disease...
  4. ncbi request reprint Isolated femoral hypoplasia: an intrauterine differential diagnosis to campomelia
    Friederike Körber
    Department of Paediatric Radiology, University of Cologne, Joseph Stelzmann Strasse 9, Cologne, Germany
    Pediatr Radiol 35:641-6. 2005
    ..Postpartum radiological examination should be reduced to a single exposure of the affected limb and follow-up should be done by clinical examination...
  5. ncbi request reprint [Occlusion of the left portal vein in newborns]
    F Korber
    Institut und Poliklinik für Radiologische Diagnostik, Kinderradiologie, Uniklinik Köln
    Ultraschall Med 32:472-8. 2011
    ..The occlusion of the left portal vein in newborn infants is shown and discussed in 14 cases...
  6. ncbi request reprint [Standardized x-ray reports of the spine in osteogenesis imperfecta]
    F Koerber
    Institut und Poliklinik für Radiologische Diagnostik, Kinderradiologie, Uniklinik Köln
    Rofo 183:462-9. 2011
    ..The parameters can be used to describe X-rays of the lateral spine and give an impartial description of anatomical structures during a treatment with bisphosphonates...
  7. ncbi request reprint A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
    Guntram Borck
    Institute of Human Genetics, University of Cologne, Kerpener Str 34, 50931, Cologne, Germany
    Hum Genet 129:45-50. 2011
    ..Thus, a phenotypic severity gradient may exist in the RAB3GAP-associated disease continuum (the "Warburg-Martsolf syndrome") which is presumably determined by the mutant gene and the nature of the mutation...