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

Year Number of Results
2000 2
2006 2
2010 1
2011 2
2012 1
2013 2
2014 1
2019 2
2020 2
2021 1
2024 0

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13 results

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Page 1
Primary hyperoxaluria type 1: still challenging!
Cochat P, Liutkus A, Fargue S, Basmaison O, Ranchin B, Rolland MO. Cochat P, et al. Among authors: basmaison o. 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.
Current approaches to the management of primary hyperoxaluria.
Cochat P, Basmaison O. Cochat P, et al. Among authors: basmaison o. Arch Dis Child. 2000 Jun;82(6):470-3. doi: 10.1136/adc.82.6.470. Arch Dis Child. 2000. PMID: 10833178 Free PMC article. Review. No abstract available.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Klein J, Buffin-Meyer B, Boizard F, Moussaoui N, Lescat O, Breuil B, Fedou C, Feuillet G, Casemayou A, Neau E, Hindryckx A, Decatte L, Levtchenko E, Raaijmakers A, Vayssière C, Goua V, Lucas C, Perrotin F, Cloarec S, Benachi A, Manca-Pellissier MC, Delmas HL, Bessenay L, Le Vaillant C, Allain-Launay E, Gondry J, Boudailliez B, Simon E, Prieur F, Lavocat MP, Saliou AH, De Parscau L, Bidat L, Noel C, Floch C, Bourdat-Michel G, Favre R, Weingertner AS, Oury JF, Baudouin V, Bory JP, Pietrement C, Fiorenza M, Massardier J, Kessler S, Lounis N, Auriol FC, Marcorelles P, Collardeau-Frachon S, Zürbig P, Mischak H, Magalhães P, Batut J, Blader P, Saulnier Blache JS, Bascands JL, Schaefer F, Decramer S, Schanstra JP; BIOMAN consortium. Klein J, et al. Kidney Int. 2021 Mar;99(3):737-749. doi: 10.1016/j.kint.2020.06.043. Epub 2020 Aug 1. Kidney Int. 2021. PMID: 32750455
[Inherited renal diseases and prenatal diagnosis].
Basmaison O, Liutkus A, Michel L, Cordier MP, Cochat P. Basmaison O, et al. Arch Pediatr. 2006 Jun;13(6):727-9. doi: 10.1016/j.arcped.2006.03.064. Epub 2006 May 11. Arch Pediatr. 2006. PMID: 16697565 French. No abstract available.
Identification of 5 novel mutations in the AGXT gene.
Basmaison O, Rolland MO, Cochat P, Bozon D. Basmaison O, et al. Hum Mutat. 2000 Jun;15(6):577. doi: 10.1002/1098-1004(200006)15:6<577::AID-HUMU9>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10862087
13 results