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[Osteoporosis in children with cerebral palsy].
Linglart A, Marchand I, Djavidi A, Senez C, Benigni I, Rothenbuhler A, Forin V. Linglart A, et al. Arch Pediatr. 2009 Jun;16(6):614-5. doi: 10.1016/S0929-693X(09)74087-4. Arch Pediatr. 2009. PMID: 19541105 French. No abstract available.
Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib.
Maupetit-Méhouas S, Mariot V, Reynès C, Bertrand G, Feillet F, Carel JC, Simon D, Bihan H, Gajdos V, Devouge E, Shenoy S, Agbo-Kpati P, Ronan A, Naud-Saudreau C, Lienhardt A, Silve C, Linglart A. Maupetit-Méhouas S, et al. Among authors: linglart a. J Med Genet. 2011 Jan;48(1):55-63. doi: 10.1136/jmg.2010.081356. Epub 2010 Oct 23. J Med Genet. 2011. PMID: 20972248 Free article.
Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance.
Linglart A, Menguy C, Couvineau A, Auzan C, Gunes Y, Cancel M, Motte E, Pinto G, Chanson P, Bougnères P, Clauser E, Silve C. Linglart A, et al. N Engl J Med. 2011 Jun 9;364(23):2218-26. doi: 10.1056/NEJMoa1012717. N Engl J Med. 2011. PMID: 21651393 Free article.
Acrodysostosis.
Silve C, Clauser E, Linglart A. Silve C, et al. Among authors: linglart a. Horm Metab Res. 2012 Sep;44(10):749-58. doi: 10.1055/s-0032-1316330. Epub 2012 Jul 19. Horm Metab Res. 2012. PMID: 22815067 Review.
245 results