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A Lienhardt

Showing results (21-30 of 27) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Relative contributions of inferior petrosal sinus sampling and pituitary imaging in the investigation of children and adolescents with ACTH-dependent Cushing's syndromeA Lienhardt, A B Grossman, J E Dacie, et al.
Hormone Research|June 16, 2001
Cushing's disease in childhood: presentation, investigation, treatment and long-term outcomeM O Savage, A Lienhardt, M C Lebrethon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 12, 2023
Evaluation of catch-up growth in severe pediatric Hashimoto's hypothyroidismA Vincent, C Bouvattier, C Teinturier, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 2014
A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism. D Kahvecioglu, B Atasay, M Berberoglu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 22, 2009
[Reflections on academic appointments in pediatrics]J Sarles, Y Aujard, A Bensman, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 21, 2021
Do children and adolescents with type 1 diabetes suffer from a lack of resources in France? Results from a benchmark study in the New Aquitaine regionM-N Campas-Lebecque, S Pochelu, V Vautier, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Relative contributions of inferior petrosal sinus sampling and pituitary imaging in the investigation of children and adolescents with ACTH-dependent Cushing's syndromeA Lienhardt, A B Grossman, J E Dacie, et al.
Hormone Research|June 16, 2001
Cushing's disease in childhood: presentation, investigation, treatment and long-term outcomeM O Savage, A Lienhardt, M C Lebrethon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 12, 2023
Evaluation of catch-up growth in severe pediatric Hashimoto's hypothyroidismA Vincent, C Bouvattier, C Teinturier, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 2014
A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism. D Kahvecioglu, B Atasay, M Berberoglu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 22, 2009
[Reflections on academic appointments in pediatrics]J Sarles, Y Aujard, A Bensman, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 21, 2021
Do children and adolescents with type 1 diabetes suffer from a lack of resources in France? Results from a benchmark study in the New Aquitaine regionM-N Campas-Lebecque, S Pochelu, V Vautier, et al.
Pageof 3