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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 diabetes
A 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 application
M 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 approach
J 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 status
F 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 hypoglycemia
L 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 review
J Chavany, A Cano, B Roquelaure, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 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 diabetes
A 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 application
M 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 approach
J 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 status
F 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 hypoglycemia
L 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 review
J Chavany, A Cano, B Roquelaure, et al.
Page
of 5