Léger J - Search Results

1

Prevalence and course of thyroid dysfunction in neonates at high risk of Graves' disease or with non-autoimmune hyperthyroidism.

Benlarbi H, Simon D, Rosenblatt J, Dumaine C, de Roux N, Chevenne D, Storey C, Poidvin A, Martinerie L, Carel JC, Léger J. Benlarbi H, et al. Among authors: leger j. Eur J Endocrinol. 2021 Mar;184(3):427-436. doi: 10.1530/EJE-20-1320. Eur J Endocrinol. 2021. PMID: 33465046

2

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

3

Adult height after long term treatment with recombinant growth hormone for idiopathic isolated growth hormone deficiency: observational follow up study of the French population based registry.

Carel JC, Ecosse E, Nicolino M, Tauber M, Leger J, Cabrol S, Bastié-Sigeac I, Chaussain JL, Coste J. Carel JC, et al. Among authors: leger j. BMJ. 2002 Jul 13;325(7355):70. doi: 10.1136/bmj.325.7355.70. BMJ. 2002. PMID: 12114235 Free PMC article.

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

Thyroid abnormalities by ultrasonography in neonates with congenital hypothyroidism.

Bubuteishvili L, Garel C, Czernichow P, Léger J. Bubuteishvili L, et al. Among authors: leger j. J Pediatr. 2003 Dec;143(6):759-64. doi: 10.1067/S0022-3476(03)00537-7. J Pediatr. 2003. PMID: 14657824

6

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

7

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

8

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

9

Proportion of various types of thyroid disorders among newborns with congenital hypothyroidism and normally located gland: a regional cohort study.

Gaudino R, Garel C, Czernichow P, Léger J. Gaudino R, et al. Among authors: leger j. Clin Endocrinol (Oxf). 2005 Apr;62(4):444-8. doi: 10.1111/j.1365-2265.2005.02239.x. Clin Endocrinol (Oxf). 2005. PMID: 15807875

10

Adult height and pubertal growth in Turner syndrome after treatment with recombinant growth hormone.

Soriano-Guillen L, Coste J, Ecosse E, Léger J, Tauber M, Cabrol S, Nicolino M, Brauner R, Chaussain JL, Carel JC. Soriano-Guillen L, et al. Among authors: leger j. J Clin Endocrinol Metab. 2005 Sep;90(9):5197-204. doi: 10.1210/jc.2005-0470. Epub 2005 Jul 5. J Clin Endocrinol Metab. 2005. PMID: 15998771

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