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Clinical Endocrinology|April 18, 2003
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 deficiencyDelphine Zenaty, Catherine Garel, Costanzo Limoni, et al.
Pflugers Archiv : European Journal of Physiology|February 9, 2017
TGF-β activates genes identified by differential mRNA display in pancreatic rudimentsTadej Battelino, Francisco Miralles, Ciril Kržišnik, et al.
The Journal of Rheumatology|December 17, 2003
Effects on growth and body composition of growth hormone treatment in children with juvenile idiopathic arthritis requiring steroid therapyDominique Simon, Nadine Lucidarme, Anne-Marie Prieur, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2007
Early recombinant human growth hormone treatment in glucocorticoid-treated children with juvenile idiopathic arthritis: a 3-year randomized studyDominique Simon, Anne-Marie Prieur, Pierre Quartier, et al.
Hormone Research|October 10, 2002
Treatment of growth failure in juvenile chronic arthritisDominique Simon, Nadine Lucidarme, Anne-Marie Prieur, et al.
Diabetes|January 29, 2002
Endocrine pancreas development in growth-retarded human fetusesFrédérique Béringue, Bertrand Blondeau, Marie Claire Castellotti, et al.
The Journal of Clinical Endocrinology and Metabolism|July 17, 2008
Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatmentFlorentia Kaguelidou, Corinne Alberti, Mireille Castanet, et al.
Pediatrics|June 5, 2003
International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24-October 1, 2001Peter A Lee, Steven D Chernausek, Anita C S Hokken-Koelega, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2002
Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidismJuliane Léger, Daniella Marinovic, Catherine Garel, et al.
The Journal of Clinical Endocrinology and Metabolism|January 19, 2006
Extending the clinical heterogeneity of iodide transport defect (ITD): a novel mutation R124H of the sodium/iodide symporter gene and review of genotype-phenotype correlations in ITDGabor Szinnai, Shinji Kosugi, Christèle Derrien, et al.
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