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R Reynaud

Showing results (31-40 of 47) with videos related to

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Annales D'Endocrinologie|February 23, 2008
[Clinical and genetic aspects of combined pituitary hormone deficiencies]F Castinetti, R Reynaud, A Saveanu, et al.
Diabetes & Metabolism|April 4, 2009
Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetesA Hartemann-Heurtier, A Simon, C Bellanné-Chantelot, et al.
International Journal of Cosmetic Science|April 5, 2019
Conformation changes in human hair keratin observed using confocal Raman spectroscopy after active ingredient applicationM Essendoubi, M Meunier, A Scandolera, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 16, 2017
Rapid differential diagnosis of diabetes insipidus in a 7-month-old infant: The copeptin approachJ Vergier, J Fromonot, A Alvares De Azevedo Macedo, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]O Delmas, C Marrec, E Caietta, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 25, 2011
[Association of type 1 diabetes mellitus and epilepsy in children. A cohort of 10 cases]E Caietta, C Halbert, A Lépine, et al.
Journal of Endocrinological Investigation|September 10, 2014
Combined pituitary hormone deficiency: current and future statusF Castinetti, R Reynaud, M-H Quentien, et al.
The Journal of Clinical Endocrinology and Metabolism|November 17, 2009
Limited value of 18F-F-DOPA PET to localize pancreatic insulin-secreting tumors in adults with hyperinsulinemic hypoglycemiaL Tessonnier, F Sebag, C Ghander, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 19, 2011
[Genetic aspects of growth hormone deficiency]R Reynaud, F Castinetti, N Galon-Faure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature reviewJ Chavany, A Cano, B Roquelaure, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Annales D'Endocrinologie|February 23, 2008
[Clinical and genetic aspects of combined pituitary hormone deficiencies]F Castinetti, R Reynaud, A Saveanu, et al.
Diabetes & Metabolism|April 4, 2009
Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetesA Hartemann-Heurtier, A Simon, C Bellanné-Chantelot, et al.
International Journal of Cosmetic Science|April 5, 2019
Conformation changes in human hair keratin observed using confocal Raman spectroscopy after active ingredient applicationM Essendoubi, M Meunier, A Scandolera, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 16, 2017
Rapid differential diagnosis of diabetes insipidus in a 7-month-old infant: The copeptin approachJ Vergier, J Fromonot, A Alvares De Azevedo Macedo, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]O Delmas, C Marrec, E Caietta, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 25, 2011
[Association of type 1 diabetes mellitus and epilepsy in children. A cohort of 10 cases]E Caietta, C Halbert, A Lépine, et al.
Journal of Endocrinological Investigation|September 10, 2014
Combined pituitary hormone deficiency: current and future statusF Castinetti, R Reynaud, M-H Quentien, et al.
The Journal of Clinical Endocrinology and Metabolism|November 17, 2009
Limited value of 18F-F-DOPA PET to localize pancreatic insulin-secreting tumors in adults with hyperinsulinemic hypoglycemiaL Tessonnier, F Sebag, C Ghander, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 19, 2011
[Genetic aspects of growth hormone deficiency]R Reynaud, F Castinetti, N Galon-Faure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature reviewJ Chavany, A Cano, B Roquelaure, et al.
Pageof 5