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Page 1
Intrafamilial Disease Heterogeneity in Primary Hyperoxaluria Type 1.
Deesker LJ, Karacoban HA, Metry EL, Garrelfs SF, Bacchetta J, Boyer O, Collard L, Devresse A, Hayes W, Hulton SA, Martin-Higueras C, Moochhala SH, Neuhaus TJ, Oh J, Prikhodina L, Sikora P, Oosterveld MJS, Groothoff JW, Mandrile G, Beck BB. Deesker LJ, et al. Among authors: garrelfs sf. Kidney Int Rep. 2024 Jul 31;9(10):3006-3015. doi: 10.1016/j.ekir.2024.07.026. eCollection 2024 Oct. Kidney Int Rep. 2024. PMID: 39430166 Free PMC article.
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium.
Metry EL, Garrelfs SF, Deesker LJ, Acquaviva C, D'Ambrosio V, Bacchetta J, Beck BB, Cochat P, Collard L, Hogan J, Ferraro PM, Franssen CFM, Harambat J, Hulton SA, Lipkin GW, Mandrile G, Martin-Higueras C, Mohebbi N, Moochhala SH, Neuhaus TJ, Prikhodina L, Salido E, Topaloglu R, Oosterveld MJS, Groothoff JW, Peters-Sengers H. Metry EL, et al. Among authors: garrelfs sf. Kidney Int Rep. 2023 Aug 4;8(10):2029-2042. doi: 10.1016/j.ekir.2023.07.025. eCollection 2023 Oct. Kidney Int Rep. 2023. PMID: 37849991 Free PMC article.
The retinal phenotype in primary hyperoxaluria type 2 and 3.
Birtel J, Diederen RM, Herrmann P, Kaspar S, Beck BB, Garrelfs SF, Hoppe B, Charbel Issa P. Birtel J, et al. Among authors: garrelfs sf. Pediatr Nephrol. 2023 May;38(5):1485-1490. doi: 10.1007/s00467-022-05765-1. Epub 2022 Oct 19. Pediatr Nephrol. 2023. PMID: 36260161 Free PMC article.
25 results