Léger J - Search Results

1

Pituitary-thyroid feedback in a patient with a sporadic activating thyrotropin (TSH) receptor mutation: implication that thyroid-secreted factors other than thyroid hormones contribute to serum TSH levels.

Gelwane G, de Roux N, Chevenne D, Carel JC, Léger J. Gelwane G, et al. Among authors: leger j. J Clin Endocrinol Metab. 2009 Aug;94(8):2787-91. doi: 10.1210/jc.2008-2524. Epub 2009 May 19. J Clin Endocrinol Metab. 2009. PMID: 19454581

2

Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidism.

Léger J, Marinovic D, Garel C, Bonaïti-Pellié C, Polak M, Czernichow P. Léger J, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):575-80. doi: 10.1210/jcem.87.2.8268. J Clin Endocrinol Metab. 2002. PMID: 11836288

3

Endocrine consequences of premature pubarche in post-pubertal Caucasian girls.

Meas T, Chevenne D, Thibaud E, Léger J, Cabrol S, Czernichow P, Lévy-Marchal C. Meas T, et al. Among authors: leger j. Clin Endocrinol (Oxf). 2002 Jul;57(1):101-6. doi: 10.1046/j.1365-2265.2002.01579.x. Clin Endocrinol (Oxf). 2002. PMID: 12100077

4

Additional phenotypic abnormalities with presence of cysts within the empty thyroid area in patients with congenital hypothyroidism with thyroid dysgenesis.

Marinovic D, Garel C, Czernichow P, Léger J. Marinovic D, et al. Among authors: leger j. J Clin Endocrinol Metab. 2003 Mar;88(3):1212-6. doi: 10.1210/jc.2002-021485. J Clin Endocrinol Metab. 2003. PMID: 12629108

5

Presence of magnetic resonance imaging abnormalities of the hypothalamic-pituitary axis is a significant determinant of the first 3 years growth response to human growth hormone treatment in prepubertal children with nonacquired growth hormone deficiency.

Zenaty D, Garel C, Limoni C, Czernichow P, Léger J. Zenaty D, et al. Among authors: leger j. Clin Endocrinol (Oxf). 2003 May;58(5):647-52. Clin Endocrinol (Oxf). 2003. PMID: 12699449

6

Sex-specific impact of congenital hypothyroidism due to thyroid dysgenesis on skeletal maturation in term newborns.

Van Vliet G, Larroque B, Bubuteishvili L, Supernant K, Léger J; Association of Française pour le Dépistage et la Prévention des Handicaps de l'Enfant. Van Vliet G, et al. Among authors: leger j. J Clin Endocrinol Metab. 2003 May;88(5):2009-13. doi: 10.1210/jc.2002-021735. J Clin Endocrinol Metab. 2003. PMID: 12727946

7

Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.

Köhler B, Lumbroso S, Leger J, Audran F, Grau ES, Kurtz F, Pinto G, Salerno M, Semitcheva T, Czernichow P, Sultan C. Köhler B, et al. Among authors: leger j. J Clin Endocrinol Metab. 2005 Jan;90(1):106-11. doi: 10.1210/jc.2004-0462. Epub 2004 Nov 2. J Clin Endocrinol Metab. 2005. PMID: 15522944

8

Do all patients with childhood-onset growth hormone deficiency (GHD) and ectopic neurohypophysis have persistent GHD in adulthood?

Léger J, Danner S, Simon D, Garel C, Czernichow P. Léger J, et al. J Clin Endocrinol Metab. 2005 Feb;90(2):650-6. doi: 10.1210/jc.2004-1274. Epub 2004 Nov 16. J Clin Endocrinol Metab. 2005. PMID: 15546901

9

Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes.

Castanet M, Sura-Trueba S, Chauty A, Carré A, de Roux N, Heath S, Léger J, Lyonnet S, Czernichow P, Polak M. Castanet M, et al. Among authors: leger j. Eur J Hum Genet. 2005 Feb;13(2):232-9. doi: 10.1038/sj.ejhg.5201321. Eur J Hum Genet. 2005. PMID: 15547625

10

Quality of life determinants in young women with turner's syndrome after growth hormone treatment: results of the StaTur population-based cohort study.

Carel JC, Ecosse E, Bastie-Sigeac I, Cabrol S, Tauber M, Léger J, Nicolino M, Brauner R, Chaussain JL, Coste J. Carel JC, et al. Among authors: leger j. J Clin Endocrinol Metab. 2005 Apr;90(4):1992-7. doi: 10.1210/jc.2004-1395. Epub 2005 Jan 11. J Clin Endocrinol Metab. 2005. PMID: 15644402

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