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

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12 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.
[Hypocalcemia and bone deformations].
Roland-Gosselin B, Basmaison O, Ranchin B, Leclerc AL, Tourab-Bouchair N, Cochat P, Bacchetta J. Roland-Gosselin B, et al. Among authors: basmaison o. Arch Pediatr. 2013 Jul;20(7):787-8, 800-2. doi: 10.1016/j.arcped.2013.04.006. Epub 2013 May 27. Arch Pediatr. 2013. PMID: 23721993 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
[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.
12 results