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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.
Primary hyperparathyroidism in pregnancy.
Diaz-Soto G, Linglart A, Sénat MV, Kamenicky P, Chanson P. Diaz-Soto G, et al. Among authors: linglart a. Endocrine. 2013 Dec;44(3):591-7. doi: 10.1007/s12020-013-9980-4. Epub 2013 May 14. Endocrine. 2013. PMID: 23670708 Review.
Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism.
Lambert AS, Grybek V, Francou B, Esterle L, Bertrand G, Bouligand J, Guiochon-Mantel A, Hieronimus S, Voitel D, Soskin S, Magdelaine C, Lienhardt A, Silve C, Linglart A. Lambert AS, et al. Among authors: linglart a. J Clin Endocrinol Metab. 2014 Mar;99(3):E469-73. doi: 10.1210/jc.2013-3136. Epub 2014 Jan 1. J Clin Endocrinol Metab. 2014. PMID: 24423332
[GACI syndrome: a case report with a neonatal beginning].
Freychet C, Gay C, Lavocat MP, Teyssier G, Patural H, Bacchetta J, Cottalorda J, Meunier BB, Linglart A, Baujat G, Stephan JL. Freychet C, et al. Among authors: linglart a. Arch Pediatr. 2014 Jun;21(6):632-6. doi: 10.1016/j.arcped.2014.03.004. Epub 2014 Apr 24. Arch Pediatr. 2014. PMID: 24768072 French.
Treatment of heterotopic ossifications secondary to pseudohypoparathyroid.
Guigonis V, Bahans C, Ea K, Bourrat E, Lienhardt A, Chabre O, Jost J, Mutar H, Ratsimbazafy V, Linglart A. Guigonis V, et al. Among authors: linglart a. Ann Endocrinol (Paris). 2015 May;76(2):183-4. doi: 10.1016/j.ando.2015.03.012. Epub 2015 Apr 24. Ann Endocrinol (Paris). 2015. PMID: 25916756 Review. No abstract available.
Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing.
Taillandier A, Domingues C, De Cazanove C, Porquet-Bordes V, Monnot S, Kiffer-Moreira T, Rothenbuhler A, Guggenbuhl P, Cormier C, Baujat G, Debiais F, Capri Y, Cohen-Solal M, Parent P, Chiesa J, Dieux A, Petit F, Roume J, Isnard M, Cormier-Daire V, Linglart A, Millán JL, Salles JP, Muti C, Simon-Bouy B, Mornet E. Taillandier A, et al. Among authors: linglart a. Mol Genet Metab. 2015 Nov;116(3):215-20. doi: 10.1016/j.ymgme.2015.09.010. Epub 2015 Sep 30. Mol Genet Metab. 2015. PMID: 26432670 Free PMC article.
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