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Ascertaining pathogenicity of genetic variants: caution required.
Arslan Z, Watson E, Bockenhauer D. Arslan Z, et al. Among authors: bockenhauer d. Pediatr Nephrol. 2023 May;38(5):1695-1696. doi: 10.1007/s00467-023-05909-x. Epub 2023 Feb 21. Pediatr Nephrol. 2023. PMID: 36809442 No abstract available.
Genetic causes of hypomagnesemia, a clinical overview.
Viering DHHM, de Baaij JHF, Walsh SB, Kleta R, Bockenhauer D. Viering DHHM, et al. Among authors: bockenhauer d. Pediatr Nephrol. 2017 Jul;32(7):1123-1135. doi: 10.1007/s00467-016-3416-3. Epub 2016 May 27. Pediatr Nephrol. 2017. PMID: 27234911 Free PMC article. Review.
Bartter and Gitelman syndromes: Questions of class.
Besouw MTP, Kleta R, Bockenhauer D. Besouw MTP, et al. Among authors: bockenhauer d. Pediatr Nephrol. 2020 Oct;35(10):1815-1824. doi: 10.1007/s00467-019-04371-y. Epub 2019 Oct 29. Pediatr Nephrol. 2020. PMID: 31664557 Free PMC article. Review.
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.
Falcone MP, Pritchard-Jones K, Brok J, Mifsud W, Williams RD, Nakata K, Tugnait S, Al-Saadi R, Side L, Anderson J, Duncan C, Marks SD, Bockenhauer D, Chowdhury T. Falcone MP, et al. Among authors: bockenhauer d. Pediatr Nephrol. 2022 Apr;37(4):821-832. doi: 10.1007/s00467-021-05125-5. Epub 2021 Oct 4. Pediatr Nephrol. 2022. PMID: 34608521 Free PMC article.
Is my PET in my genes?
Downie M, Shroff R, Bockenhauer D. Downie M, et al. Among authors: bockenhauer d. Pediatr Nephrol. 2022 Jun;37(6):1175-1178. doi: 10.1007/s00467-022-05452-1. Epub 2022 Jan 25. Pediatr Nephrol. 2022. PMID: 35079873 No abstract available.
260 results