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Page 1
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope.
Groothoff JW, Metry E, Deesker L, Garrelfs S, Acquaviva C, Almardini R, Beck BB, Boyer O, Cerkauskiene R, Ferraro PM, Groen LA, Gupta A, Knebelmann B, Mandrile G, Moochhala SS, Prytula A, Putnik J, Rumsby G, Soliman NA, Somani B, Bacchetta J. Groothoff JW, et al. Among authors: acquaviva c. Nat Rev Nephrol. 2023 Mar;19(3):194-211. doi: 10.1038/s41581-022-00661-1. Epub 2023 Jan 5. Nat Rev Nephrol. 2023. PMID: 36604599 Review.
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: acquaviva c. 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.
Circulating Oxalate Levels in Short Bowel Syndrome as a Severity Marker of CKD.
Grocholski C, Chambrier C, Lauverjat M, Acquaviva C, Abid N, Bergoin C, Guebre-Egziabher F, Bacchetta J, Derain-Dubourg L, De Mul A, Lemoine S. Grocholski C, et al. Among authors: acquaviva c. Kidney Int Rep. 2023 Dec 28;9(3):686-693. doi: 10.1016/j.ekir.2023.12.023. eCollection 2024 Mar. Kidney Int Rep. 2023. PMID: 38481504 Free PMC article.
Elastin turnover in Williams-Beuren and 7q11.23 microduplication syndromes.
Guilhem A, Ruet S, Edery P, Acquaviva C, Rossi M. Guilhem A, et al. Among authors: acquaviva c. Eur Heart J Open. 2024 Jun 13;4(3):oeae045. doi: 10.1093/ehjopen/oeae045. eCollection 2024 May. Eur Heart J Open. 2024. PMID: 38948347 Free PMC article. No abstract available.
Primary hyperoxaluria in adults and children: a nationwide cohort highlights a persistent diagnostic delay.
Pszczolinski R, Acquaviva C, Berrahal I, Biebuyck N, Burtey S, Clabault K, Dossier C, Guillet M, Hemery F, Letavernier E, Rousset-Rouvière C, Bacchetta J, Moulin B. Pszczolinski R, et al. Among authors: acquaviva c. Clin Kidney J. 2024 Apr 3;17(5):sfae099. doi: 10.1093/ckj/sfae099. eCollection 2024 May. Clin Kidney J. 2024. PMID: 38737343 Free PMC article.
Genetic assessment in primary hyperoxaluria: why it matters.
Mandrile G, Beck B, Acquaviva C, Rumsby G, Deesker L, Garrelfs S, Gupta A, Bacchetta J, Groothoff J; OxalEurope Consortium/Erknet Guideline Workgroup On Hyperoxaluria. Mandrile G, et al. Among authors: acquaviva c. Pediatr Nephrol. 2023 Mar;38(3):625-634. doi: 10.1007/s00467-022-05613-2. Epub 2022 Jun 13. Pediatr Nephrol. 2023. PMID: 35695965 Free PMC article. Review.
Very long-term outcomes in 23 patients with cblA type methylmalonic acidemia.
Marelli C, Fouilhoux A, Benoist JF, De Lonlay P, Guffon-Fouilhoux N, Brassier A, Cano A, Chabrol B, Pennisi A, Schiff M, Acquaviva C, Murphy E, Servais A, Lachmann R. Marelli C, et al. Among authors: acquaviva c. J Inherit Metab Dis. 2022 Sep;45(5):937-951. doi: 10.1002/jimd.12525. Epub 2022 Jun 23. J Inherit Metab Dis. 2022. PMID: 35618652 Free PMC article.
102 results