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Page 1
[Pigmented villonodular synovitis in children: review of six cases].
Pannier S, Odent T, Milet A, Lambot-Juhan K, Glorion C. Pannier S, et al. Rev Chir Orthop Reparatrice Appar Mot. 2008 Feb;94(1):64-72. doi: 10.1016/j.rco.2007.07.007. Epub 2008 Feb 20. Rev Chir Orthop Reparatrice Appar Mot. 2008. PMID: 18342032 French.
Characterization and prevalence of severe primary IGF1 deficiency in a large cohort of French children with short stature.
Teissier R, Flechtner I, Colmenares A, Lambot-Juhan K, Baujat G, Pauwels C, Samara-Boustani D, Beltrand J, Simon A, Thalassinos C, Crosnier H, Latrech H, Pinto G, Le Merrer M, Cormier-Daire V, Souberbielle JC, Polak M. Teissier R, et al. Among authors: lambot juhan k. Eur J Endocrinol. 2014 Jun;170(6):847-54. doi: 10.1530/EJE-14-0071. Epub 2014 Mar 24. Eur J Endocrinol. 2014. PMID: 24662318
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients.
Flechtner I, Lambot-Juhan K, Teissier R, Colmenares A, Baujat G, Beltrand J, Ajaltouni Z, Pauwels C, Pinto G, Samara-Boustani D, Simon A, Thalassinos C, Le Merrer M, Cormier-Daire V, Polak M. Flechtner I, et al. Among authors: lambot juhan k. Eur J Endocrinol. 2014 Apr 10;170(5):677-84. doi: 10.1530/EJE-13-0864. Print 2014 May. Eur J Endocrinol. 2014. PMID: 24536087
Expanding the skeletal phenotype of Loeys-Dietz syndrome.
Sousa SB, Lambot-Juhan K, Rio M, Baujat G, Topouchian V, Hanna N, Le Merrer M, Brunelle F, Munnich A, Boileau C, Cormier-Daire V. Sousa SB, et al. Am J Med Genet A. 2011 May;155A(5):1178-83. doi: 10.1002/ajmg.a.33813. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484991 No abstract available.
14 results