Long-term auxological and pubertal outcome of patients with hereditary insulin-like growth factor-I deficiency (Laron and growth hormone-gene deletion syndrome) treated with recombinant human insulin-like growth factor-I

Author:

Messina M. F.,Arrigo T.,Valenzise M.,Ghizzoni L.,Caruso-Nicoletti M.,Zucchini S.,Chiabotto P.,Crisafulli G.,Zirilli G.,De Luca F.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Chandrashekar V, Bartke A. The role of insulin-like growth factor-I in neuroendocrine function and the consequent effect on sexual maturation: inferences from animal models. Reprod Biol 2003, 3: 7–28.

2. Vendola K, Zhon J, Wang J, Bondy CA. Androgens promote insulin-like growth factor-I and insulin-like growth factor-I receptor gene expression in the primate ovary. Hum Reprod 1999, 14: 2328–32.

3. Bondy C, Werner H, Roberts CT, Le Roith D. Cellular pattern of type-I insulin-like growth factor receptor gene expression during maturation of the rat brain: comparison with insulin-like growth factor I and II. Neuroscience 1992, 46: 909–23.

4. Daftary SS, Gore AC. IGF-1 in the brain as a regulator of reproductive neuroendocrine function. Exp Biol Med 2005, 230: 292–306.

5. Laron Z. Development and biological function of the female gonads and genitalia in IGF-I deficiency — Laron syndrome as a model. Pediatr Endocrinol Rev 2006, 3 (Suppl 1): 188–91.

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