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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1992 1
1994 1
1996 2
1999 1
2000 1
2001 1
2002 4
2003 1
2004 3
2005 4
2006 6
2007 5
2008 7
2009 14
2010 10
2011 13
2012 9
2013 10
2014 6
2015 6
2016 5
2017 11
2018 9
2019 15
2020 13
2021 13
2022 11
2023 14

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172 results

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Page 1
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Andersen CBF, Bergmann C, Antignac C, Simons M. Bedin M, et al. Among authors: ranchin b. J Clin Invest. 2020 Jan 2;130(1):335-344. doi: 10.1172/JCI129937. J Clin Invest. 2020. PMID: 31613795 Free PMC article. Clinical Trial.
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. Among authors: ranchin b. 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
[Renal abnormalities in Down syndrome: A review].
Niamien-Attai C, Bacchetta J, Ranchin B, Sanlaville D, Cochat P. Niamien-Attai C, et al. Among authors: ranchin b. Arch Pediatr. 2017 Oct;24(10):1013-1018. doi: 10.1016/j.arcped.2017.07.014. Arch Pediatr. 2017. PMID: 28893484 Review. French.
Eplet incompatibility in pediatric renal transplantation.
Rãchişan AL, Dubois V, Ranchin B, Sellier-Leclerc AL, Bertholet Thomas A, Cochat P, Bacchetta J. Rãchişan AL, et al. Among authors: ranchin b. Pediatr Transplant. 2020 Sep;24(6):e13721. doi: 10.1111/petr.13721. Epub 2020 May 10. Pediatr Transplant. 2020. PMID: 32388894
Disease recurrence in paediatric renal transplantation.
Cochat P, Fargue S, Mestrallet G, Jungraithmayr T, Koch-Nogueira P, Ranchin B, Zimmerhackl LB. Cochat P, et al. Among authors: ranchin b. Pediatr Nephrol. 2009 Nov;24(11):2097-108. doi: 10.1007/s00467-009-1137-6. Epub 2009 Feb 27. Pediatr Nephrol. 2009. PMID: 19247694 Free PMC article. Review.
[Vitamin D revisited: a cornerstone of health?].
Bacchetta J, Ranchin B, Dubourg L, Cochat P. Bacchetta J, et al. Among authors: ranchin b. Arch Pediatr. 2010 Dec;17(12):1687-95. doi: 10.1016/j.arcped.2010.09.003. Epub 2010 Oct 14. Arch Pediatr. 2010. PMID: 20951011 Review. French.
Primary hyperoxaluria type 1: still challenging!
Cochat P, Liutkus A, Fargue S, Basmaison O, Ranchin B, Rolland MO. Cochat P, et al. Among authors: ranchin b. Pediatr Nephrol. 2006 Aug;21(8):1075-81. doi: 10.1007/s00467-006-0124-4. Epub 2006 Jun 30. Pediatr Nephrol. 2006. PMID: 16810517 Review.
172 results