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Page 1
["New renal insufficiencies"].
Cochat P, Dubourg L, Ranchin B, Fauriel I, Guffon N, Liutkus A. Cochat P, et al. Arch Pediatr. 2001 May;8 Suppl 2:317s-318s. doi: 10.1016/s0929-693x(01)80058-0. Arch Pediatr. 2001. PMID: 11394100 French. No abstract available.
New ocular phenotype associated with a mutation in the PAX2 gene.
Beby F, Roche O, Cochat P, Ranchin B, Kohler R, Bonifas C, Cordier MP, Attie-Bitach T, Burillon C, Denis P. Beby F, et al. Among authors: cochat p. Eye (Lond). 2010 Jul;24(7):1293-4. doi: 10.1038/eye.2009.330. Epub 2010 Jan 15. Eye (Lond). 2010. PMID: 20075965 No abstract available.
Familial infantile nephrotic syndrome with ocular abnormalities.
Glastre C, Cochat P, Bouvier R, Colon S, Cottin X, Giffon D, Wright C, Dijoud F, David L. Glastre C, et al. Among authors: cochat p. Pediatr Nephrol. 1990 Jul;4(4):340-2. doi: 10.1007/BF00862514. Pediatr Nephrol. 1990. PMID: 2206901
[Paediatric nephrology in developing countries].
Cochat P, Cazet F, Liutkus A, Mourani C, Exantus J, Akatcherian C. Cochat P, et al. Arch Pediatr. 2005 Jun;12(6):723-5. doi: 10.1016/j.arcped.2005.04.061. Arch Pediatr. 2005. PMID: 15904784 French. No abstract available.
[MURCS association: a challenging diagnosis].
Vergnes C, Cordier MP, Dubois R, Bouvier R, Cochat P. Vergnes C, et al. Among authors: cochat p. Arch Pediatr. 2005 Jan;12(1):49-51. doi: 10.1016/j.arcped.2004.09.012. Arch Pediatr. 2005. PMID: 15653055 French.
484 results