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The Journal of Clinical Endocrinology and Metabolism
|
October 8, 2010
Elevated insulin-like growth factor-I values in children with Prader-Willi syndrome compared with growth hormone (GH) deficiency children over two years of GH treatment
Eva Feigerlová, Gwenaëlle Diene, Isabelle Oliver, et al.
Hormone Research
|
November 2, 2005
Long-term evolution of endocrine disorders and effect of GH therapy in 35 patients with pituitary stalk interruption syndrome
Maïthé Tauber, Jean Chevrel, Gwenaelle Diene, et al.
Hormone Research in Paediatrics
|
April 18, 2012
Gender influences short-term growth hormone treatment response in children
Lars Sävendahl, Oliver Blankenstein, Isabelle Oliver, et al.
World Journal of Surgical Oncology
|
August 12, 2018
Wilms tumor, pleuropulmonary blastoma, and DICER1: case report and literature review
Olivier Abbo, Kalitha Pinnagoda, Laurent Brouchet, et al.
Clinical Endocrinology
|
August 14, 2019
Multinodular goitre is a gateway for molecular testing of DICER1 syndrome
Isabelle Oliver-Petit, Anne-Isabelle Bertozzi, Solange Grunenwald, et al.
International Journal of Pediatric Endocrinology
|
July 14, 2012
Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies
Peter A Lee, Lars Sävendahl, Isabelle Oliver, et al.
Bulletin Du Cancer
|
October 16, 2019
[DICER1 constitutional pathogenic variant syndrome: Where are we in 2019?]
Yves Réguerre, Lisa Golmard, Hervé J Brisse, et al.
Bone
|
September 7, 2021
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levels
Marine Delagrange, Vanessa Rousseau, Catie Cessans, et al.
Plos One
|
November 13, 2015
Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation
Céline Bar, Charline Zadro, Gwenaelle Diene, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 7, 2003
Adolescents with partial growth hormone (GH) deficiency develop alterations of body composition after GH discontinuation and require follow-up
Maithé Tauber, Béatrice Jouret, Audrey Cartault, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
The Journal of Clinical Endocrinology and Metabolism
|
October 8, 2010
Elevated insulin-like growth factor-I values in children with Prader-Willi syndrome compared with growth hormone (GH) deficiency children over two years of GH treatment
Eva Feigerlová, Gwenaëlle Diene, Isabelle Oliver, et al.
Hormone Research
|
November 2, 2005
Long-term evolution of endocrine disorders and effect of GH therapy in 35 patients with pituitary stalk interruption syndrome
Maïthé Tauber, Jean Chevrel, Gwenaelle Diene, et al.
Hormone Research in Paediatrics
|
April 18, 2012
Gender influences short-term growth hormone treatment response in children
Lars Sävendahl, Oliver Blankenstein, Isabelle Oliver, et al.
World Journal of Surgical Oncology
|
August 12, 2018
Wilms tumor, pleuropulmonary blastoma, and DICER1: case report and literature review
Olivier Abbo, Kalitha Pinnagoda, Laurent Brouchet, et al.
Clinical Endocrinology
|
August 14, 2019
Multinodular goitre is a gateway for molecular testing of DICER1 syndrome
Isabelle Oliver-Petit, Anne-Isabelle Bertozzi, Solange Grunenwald, et al.
International Journal of Pediatric Endocrinology
|
July 14, 2012
Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies
Peter A Lee, Lars Sävendahl, Isabelle Oliver, et al.
Bulletin Du Cancer
|
October 16, 2019
[DICER1 constitutional pathogenic variant syndrome: Where are we in 2019?]
Yves Réguerre, Lisa Golmard, Hervé J Brisse, et al.
Bone
|
September 7, 2021
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levels
Marine Delagrange, Vanessa Rousseau, Catie Cessans, et al.
Plos One
|
November 13, 2015
Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation
Céline Bar, Charline Zadro, Gwenaelle Diene, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 7, 2003
Adolescents with partial growth hormone (GH) deficiency develop alterations of body composition after GH discontinuation and require follow-up
Maithé Tauber, Béatrice Jouret, Audrey Cartault, et al.
Page
of 4