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The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Biochimica Et Biophysica Acta|September 15, 2009
Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1)J Poulton, M Hirano, A Spinazzola, et al.
Clinical Chemistry|November 1, 1996
Development of human renal function: reference intervals for 10 biochemical markers in fetal urineF Muller, M Dommergues, L Bussières, et al.
Nephrologie|January 1, 1996
[Value of cyclosporine in the treatment of the recurrence of nephrosis after renal transplantation]B Ranchin, M F Gagnadoux, M Broyer, et al.
The New England Journal of Medicine|January 6, 1994
Effect of plasma protein adsorption on protein excretion in kidney-transplant recipients with recurrent nephrotic syndromeJ Dantal, E Bigot, W Bogers, et al.
Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.
The New England Journal of Medicine|May 23, 1991
Anti-B-cell monoclonal antibodies in the treatment of severe B-cell lymphoproliferative syndrome following bone marrow and organ transplantationA Fischer, S Blanche, J Le Bidois, et al.
The Journal of Urology|August 8, 2001
Urological complications after renal transplantation using ureteroureteral anastomosis in childrenS P Lapointe, M Charbit, D Jan, et al.
Kidney International|May 3, 2000
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosisE Denamur, N Bocquet, V Baudouin, et al.
Nature Genetics|December 17, 1997
Donor splice-site mutations in WT1 are responsible for Frasier syndromeS Barbaux, P Niaudet, M C Gubler, et al.
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