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Year Number of Results
1952 1
1997 1
1998 2
2000 2
2001 5
2002 2
2003 6
2004 1
2005 3
2006 5
2007 1
2008 3
2009 4
2010 7
2011 7
2012 5
2013 3
2014 3
2015 4
2016 8
2017 9
2018 6
2019 5
2020 4
2021 6
2022 4
2023 5
2024 2

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99 results

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Page 1
[RT-PCR in clinical diagnosis].
Cavé H, Acquaviva C, Bièche I, Brault D, de Fraipont F, Fina F, Loric S, Maisonneuve L, Namour F, Tuffery S. Cavé H, et al. Among authors: acquaviva c. Ann Biol Clin (Paris). 2003 Nov-Dec;61(6):635-44. Ann Biol Clin (Paris). 2003. PMID: 14711604 Free article. Review. French.
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.
The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT.
Coughlin CR 2nd, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodríguez-Pombo P, Väisänen ML, Spector E, Creadon-Swindell G, Brás-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, Pérez-Cerdá C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. Coughlin CR 2nd, et al. Among authors: acquaviva c. Genet Med. 2017 Jan;19(1):104-111. doi: 10.1038/gim.2016.74. Epub 2016 Jun 30. Genet Med. 2017. PMID: 27362913 Free article.
Primary hyperoxaluria.
Harambat J, Fargue S, Bacchetta J, Acquaviva C, Cochat P. Harambat J, et al. Among authors: acquaviva c. Int J Nephrol. 2011;2011:864580. doi: 10.4061/2011/864580. Epub 2011 Jun 16. Int J Nephrol. 2011. PMID: 21748001 Free PMC article.
Complex mechanisms for c-fos and c-jun degradation.
Jariel-Encontre I, Salvat C, Steff AM, Pariat M, Acquaviva C, Furstoss O, Piechaczyk M. Jariel-Encontre I, et al. Among authors: acquaviva c. Mol Biol Rep. 1997 Mar;24(1-2):51-6. doi: 10.1023/a:1006804723722. Mol Biol Rep. 1997. PMID: 9228281 Review.
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.
Multiple degradation pathways for Fos family proteins.
Acquaviva C, Bossis G, Ferrara P, Brockly F, Jariel-Encontre I, Piechaczyk M. Acquaviva C, et al. Ann N Y Acad Sci. 2002 Nov;973:426-34. doi: 10.1111/j.1749-6632.2002.tb04677.x. Ann N Y Acad Sci. 2002. PMID: 12485905 Review.
Myelodysplastic syndromes: lost between two states?
Acquaviva C, Gelsi-Boyer V, Birnbaum D. Acquaviva C, et al. Leukemia. 2010 Jan;24(1):1-5. doi: 10.1038/leu.2009.157. Leukemia. 2010. PMID: 20068572 No abstract available.
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.
99 results