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American Journal of Human Genetics|July 27, 1999
Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assayL Forestier, G Jean, M Attard, et al.
Pediatric Nephrology (Berlin, Germany)|January 17, 2002
Long term results of liver-kidney transplantation in children with primary hyperoxaluriaM F Gagnadoux, F Lacaille, P Niaudet, et al.
American Journal of Medical Genetics|May 22, 1995
Craniosynostosis and kidney malformation in a case of Hennekam syndromeV Cormier-Daire, S Lyonnet, A Lehnert, et al.
Archives Francaises De Pediatrie|November 1, 1979
[Nephrotic syndrome, antithrombin III deficiency and recurrent thrombosis. The value of vitamin K antagonists]M Guillot, A M Fischer, D Goldszmidt, et al.
Annales De Pediatrie|February 1, 1990
[Nail-patella syndrome without extra-renal lesions. A new hereditary glomerular nephropathy]M C Gubler, J P Dommergues, J Furioli, et al.
Faraday Discussions|May 2, 2008
Optical properties and relaxation processes at femtosecond scale of bimetallic clustersM Broyer, E Cottancin, J Lermé, et al.
Archives Francaises De Pediatrie|March 1, 1985
[Circulating metabolites of vitamin D in 14 children with hypercalcemia]E Jacqz, M Garabedian, H Guillozo, et al.
Orthopaedic Review|May 1, 1992
Tarsal tunnel syndrome secondary to neurilemmomaJ L Tedder, H P Insler, R Antoine
The New England Journal of Medicine|April 11, 1985
Elevated plasma 1,25-dihydroxyvitamin D concentrations in infants with hypercalcemia and an elfin faciesM Garabédian, E Jacqz, H Guillozo, et al.
Pediatrie|January 1, 1993
[Effectiveness of and tolerance to human recombinant erythropoietin in the treatment of kidney failure anemia in children undergoing continuous peritoneal dialysis. Multicenter study]B Parchoux, M Broyer, P Cochat, et al.
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