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Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.
Harambat J, Fargue S, Acquaviva C, Gagnadoux MF, Janssen F, Liutkus A, Mourani C, Macher MA, Abramowicz D, Legendre C, Durrbach A, Tsimaratos M, Nivet H, Girardin E, Schott AM, Rolland MO, Cochat P. Harambat J, et al. Among authors: girardin e. Kidney Int. 2010 Mar;77(5):443-9. doi: 10.1038/ki.2009.435. Epub 2009 Dec 16. Kidney Int. 2010. PMID: 20016466 Free article.
Long-term outcome of idiopathic steroid-resistant nephrotic syndrome: a multicenter study.
Mekahli D, Liutkus A, Ranchin B, Yu A, Bessenay L, Girardin E, Van Damme-Lombaerts R, Palcoux JB, Cachat F, Lavocat MP, Bourdat-Michel G, Nobili F, Cochat P. Mekahli D, et al. Among authors: girardin e. Pediatr Nephrol. 2009 Aug;24(8):1525-32. doi: 10.1007/s00467-009-1138-5. Epub 2009 Mar 12. Pediatr Nephrol. 2009. PMID: 19280229
Two new families with hereditary minimal change disease.
Chehade H, Cachat F, Girardin E, Rotman S, Correia AJ, Fellmann F, Bonny O. Chehade H, et al. Among authors: girardin e. BMC Nephrol. 2013 Mar 22;14:65. doi: 10.1186/1471-2369-14-65. BMC Nephrol. 2013. PMID: 23517548 Free PMC article.
110 results