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Page 1
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K; ESCAPE Study group; GPN study group; Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium. Burgmaier K, et al. Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30. Kidney Int. 2021. PMID: 33940108
Kidney and vascular involvement in Alagille syndrome.
Ranchin B, Meaux MN, Freppel M, Ruiz M, De Mul A. Ranchin B, et al. Among authors: de mul a. Pediatr Nephrol. 2025 Apr;40(4):891-899. doi: 10.1007/s00467-024-06562-8. Epub 2024 Oct 24. Pediatr Nephrol. 2025. PMID: 39446153 Free PMC article. Review.
Multiparametric MRI: can we assess renal function differently?
Tournebize C, Schleef M, De Mul A, Pacaud S, Derain-Dubourg L, Juillard L, Rouvière O, Lemoine S. Tournebize C, et al. Among authors: de mul a. Clin Kidney J. 2024 Nov 19;18(1):sfae365. doi: 10.1093/ckj/sfae365. eCollection 2025 Jan. Clin Kidney J. 2024. PMID: 40008350 Free PMC article. Review.
[Medullary sponge kidney: a pathology still full of unknowns].
Tournebize C, Abid N, De Mul A, Schleef M, Derain-Dubourg L, Lemoine S. Tournebize C, et al. Among authors: de mul a. Nephrol Ther. 2024 Dec 1;20(7):641-649. doi: 10.1684/ndt.2024.98. Nephrol Ther. 2024. PMID: 39917789 Review. French.
[Management of patients with kidney stones].
De-Mul A, Bacchetta J, Lemoine S. De-Mul A, et al. Nephrol Ther. 2024 Dec 1;20(7):650-657. doi: 10.1684/ndt.2024.102. Nephrol Ther. 2024. PMID: 39917790 French.
45 results