Maite Tauber
Toulouse, France
Last Updated: 09/26/2026
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Found 8 publications
Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study.
Journal: Therapeutic advances in endocrinology and metabolism
Published: June 02, 2023
Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.
Journal: European journal of medical genetics
Published: June 13, 2019
Growth hormone in combination with leuprorelin in pubertal children with idiopathic short stature.
Journal: Endocrine connections
Published: April 11, 2018
Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated Patients.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 01, 2016
Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature.
Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature.
Journal: American journal of medical genetics. Part A
Published: July 06, 2016
Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 29, 2012
Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children.
Journal: Journal of physiology and biochemistry
Published: January 04, 2012
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Last Updated: 09/26/2026