Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up

  1. Garrelfs, S.F. 1
  2. Rumsby, G. 2
  3. Peters-Sengers, H. 1
  4. Erger, F. 3
  5. Groothoff, J.W. 1
  6. Beck, B.B. 3
  7. Oosterveld, M.J.S. 1
  8. Pelle, A. 4
  9. Neuhaus, T. 5
  10. Adams, B. 6
  11. Cochat, P. 7
  12. Salido, E. 8
  13. Lipkin, G.W. 9
  14. Hoppe, B. 10
  15. Hulton, S.-A. 11
  1. 1 University of Amsterdam
    info

    University of Amsterdam

    Ámsterdam, Holanda

    GRID grid.7177.6

  2. 2 University College London
    info

    University College London

    Londres, Reino Unido

    GRID grid.83440.3b

  3. 3 Institute of Human Genetics, Center for Molecular Medicine Cologne, and Center for Rare and hereditary Kidney Disease, Cologne, University Hospital of Cologne
  4. 4 Medical Genetics Unit, San Luigi University Hospital, Orbassano
  5. 5 Department of Pediatrics, Children's Hospital Lucerne
  6. 6 Department of Pediatric Nephrology, Hôpital Universitaire des Enfants-Reine Fabiola, Université Libre de Bruxelles
  7. 7 Department of Pediatric Nephrology, Hospices Civils de Lyon and University de Lyon
  8. 8 Hospital Universitario de Canarias
    info

    Hospital Universitario de Canarias

    San Cristóbal de La Laguna, España

    GRID grid.411220.4

  9. 9 Department of Nephrology, University Hospitals Birmingham NHS Foundation Trust
  10. 10 University of Bonn
    info

    University of Bonn

    Bonn, Alemania

    GRID grid.10388.32

  11. 11 Department of Nephrology, Birmingham Children's Hospital NHS Foundation Trust
Journal:
Kidney International

ISSN: 1523-1755

Year of publication: 2019

Volume: 96

Issue: 6

Pages: 1389-1399

Type: Article

Export: RIS
DOI: 10.1016/j.kint.2019.08.018 PMID: 31685312 SCOPUS: 2-s2.0-85074520141 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus