Sfoglia per AUTORE
BECK B
Collezione AOU San Luigi di Orbassano

  

Items : 9

Intrafamilial Disease Heterogeneity in Primary Hyperoxaluria Type 1. in Kidney international reports / Kidney Int Rep. 2024 Jul 31;9(10):3006-3015. doi: 10.1016/j.ekir.2024.07.026. eCollection 2024 Oct.
2024
AOU San Luigi di Orbassano

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;

Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium. in Kidney international reports / Kidney Int Rep. 2023 Aug 4;8(10):2029-2042. doi: 10.1016/j.ekir.2023.07.025. eCollection 2023 Oct.
2023
AOU San Luigi di Orbassano

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;

Genetic assessment in primary hyperoxaluria: why it matters. in Pediatric nephrology (Berlin, Germany) / Pediatr Nephrol. 2023 Mar;38(3):625-634. doi: 10.1007/s00467-022-05613-2. Epub 2022 Jun 13.
2023
ASL Torino 4
AOU San Luigi di Orbassano

Gupta A; Bacchetta J; Groothoff J; Garrelfs S; Deesker L; Rumsby G; Acquaviva C; Beck B; Mandrile G;

Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope. in Nature reviews. Nephrology / Nat Rev Nephrol. 2023 Mar;19(3):194-211. doi: 10.1038/s41581-022-00661-1. Epub 2023 Jan 5.
2023
AOU San Luigi di Orbassano

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;

Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry. in Kidney international reports / Kidney Int Rep. 2022 Apr 20;7(7):1608-1618. doi: 10.1016/j.ekir.2022.04.012. eCollection 2022 Jul.
2022
ASL Torino 4
AOU San Luigi di Orbassano

Neuhaus T; Salido E; Prikhodina L; Topaloglu R; Collard L; Beck BB; Hoppe B; Gupta A; Hulton SA; Harambat J; Deschênes G; Cochat P; Oosterveld MJS; Mandrile G; Garrelfs SF; Deesker LJ; Groothoff JW; Bacchetta J;

Long-Term Transplantation Outcomes in Patients With Primary Hyperoxaluria Type 1 Included in the European Hyperoxaluria Consortium (OxalEurope) Registry. in Kidney international reports / Kidney Int Rep. 2021 Nov 26;7(2):210-220. doi: 10.1016/j.ekir.2021.11.006. eCollection 2022 Feb.
2022
ASL Torino 4
AOU San Luigi di Orbassano

Cochat P; Prikhodina L; Hoppe B; Oosterveld MJS; Moochhala SH; Mohebbi N; Mandrile G; Lipkin GW; Kemper MJ; Franssen C; Deschênes G; Collard L; Beck BB; Bacchetta J; Acquaviva C; Hulton SA; Peters-Sengers H; Garrelfs SF; Metry EL; Groothoff JW;

Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up. in Kidney international / Kidney Int. 2019 Dec;96(6):1389-1399. doi: 10.1016/j.kint.2019.08.018. Epub 2019 Sep 3.
2019
AOU San Luigi di Orbassano

Salido E; Cochat P; Adams B; Pelle A; Neuhaus T; Oosterveld MJS; Beck BB; Groothoff JW; Erger F; Peters-Sengers H; Rumsby G; Garrelfs SF; Lipkin GW; Hoppe B; Hulton SA;

Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type. in Kidney international / Kidney Int. 2014 Dec;86(6):1197-204. doi: 10.1038/ki.2014.222. Epub 2014 Jul 2.
2014
AOU San Luigi di Orbassano

Mandrile G; van Woerden CS; Berchialla P; Beck BB; Acquaviva Bourdain C; Hulton SA; Rumsby G;

Novel human pathological mutations. Gene symbol: AGXT. Disease: hyperoxaluria. in Human genetics / Hum Genet. 2010 Apr;127(4):468.
2010
AOU San Luigi di Orbassano

Robbiano A; Mandrile G; De Marchi M; Beck B; Baasner A; Murer L; Benetti E; Giachino D;