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296 results

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Page 1
Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.
Zenker M, Aigner T, Wendler O, Tralau T, Müntefering H, Fenski R, Pitz S, Schumacher V, Royer-Pokora B, Wühl E, Cochat P, Bouvier R, Kraus C, Mark K, Madlon H, Dötsch J, Rascher W, Maruniak-Chudek I, Lennert T, Neumann LM, Reis A. Zenker M, et al. Among authors: bouvier r. Hum Mol Genet. 2004 Nov 1;13(21):2625-32. doi: 10.1093/hmg/ddh284. Epub 2004 Sep 14. Hum Mol Genet. 2004. PMID: 15367484
Recurrence of a dysgerminoma in Frasier syndrome.
Mestrallet G, Bertholet-Thomas A, Ranchin B, Bouvier R, Frappaz D, Cochat P. Mestrallet G, et al. Among authors: bouvier r. Pediatr Transplant. 2011 May;15(3):e53-5. doi: 10.1111/j.1399-3046.2010.01273.x. Pediatr Transplant. 2011. PMID: 20408995
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: bouvier r. Pediatr Nephrol. 1990 Jul;4(4):340-2. doi: 10.1007/BF00862514. Pediatr Nephrol. 1990. PMID: 2206901
[MURCS association: a challenging diagnosis].
Vergnes C, Cordier MP, Dubois R, Bouvier R, Cochat P. Vergnes C, et al. Among authors: bouvier r. Arch Pediatr. 2005 Jan;12(1):49-51. doi: 10.1016/j.arcped.2004.09.012. Arch Pediatr. 2005. PMID: 15653055 French.
Fetal phenotype associated with the 22q11 deletion.
Noël AC, Pelluard F, Delezoide AL, Devisme L, Loeuillet L, Leroy B, Martin A, Bouvier R, Laquerriere A, Jeanne-Pasquier C, Bessieres-Grattagliano B, Mechler C, Alanio E, Leroy C, Gaillard D. Noël AC, et al. Among authors: bouvier r. Am J Med Genet A. 2014 Nov;164A(11):2724-31. doi: 10.1002/ajmg.a.36720. Epub 2014 Aug 8. Am J Med Genet A. 2014. PMID: 25111715
Nephronophthisis-like nephritis associated with fibrous dysplasia of bone.
Bacchetta J, Chapurlat R, Bouvier R, Antignac C, Dubourg L, Kohler R, Delmas PD, Cochat P. Bacchetta J, et al. Among authors: bouvier r. Pediatr Nephrol. 2008 Sep;23(9):1559-63. doi: 10.1007/s00467-008-0850-x. Epub 2008 May 30. Pediatr Nephrol. 2008. PMID: 18512082
'Renal hypersensitivity' to inulin and IgA nephropathy.
Bacchetta J, Villard F, Vial T, Dubourg L, Bouvier R, Kassaï B, Cochat P. Bacchetta J, et al. Among authors: bouvier r. Pediatr Nephrol. 2008 Oct;23(10):1883-5. doi: 10.1007/s00467-008-0819-9. Epub 2008 Jun 6. Pediatr Nephrol. 2008. PMID: 18535847
[Renal tubular dysgenesis and mutation in the renin gene].
Bacchetta J, Dijoud F, Bouvier R, Putet G, Gubler MC, Cochat P. Bacchetta J, et al. Among authors: bouvier r. Arch Pediatr. 2007 Sep;14(9):1084-7. doi: 10.1016/j.arcped.2007.04.012. Epub 2007 Jun 6. Arch Pediatr. 2007. PMID: 17555949 French.
296 results