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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 15, 2004
[Bone mineral metabolism: recent data and perspectives related to osteogenesis]I Gennero, P Moulin, T Edouard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 7, 2018
Laboratory diagnosis of hypophosphatasiaI Gennero, F Conte-Auriol, J-P Salles
European Journal of Endocrinology|May 7, 2009
Prevalence of IGF1 deficiency in prepubertal children with isolated short statureT Edouard, S Grünenwald, I Gennero, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 22, 2008
[New molecular mechanisms of growth hormone insensitivity]T Edouard, P Raynal, A Yart, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 22, 2008
[Growth follow-up of SGA children after 3 years of GH treatment]T Edouard, I Oliver, B Jouret, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 3, 2017
[Severe nutritional rickets in young children: Resurgence of an old disease]S Estrade, C Majorel, N Tahhan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 7, 2009
[Delayed puberty]T Edouard, M Tauber
Cellular and Molecular Life Sciences : CMLS|April 25, 2007
How do Shp2 mutations that oppositely influence its biochemical activity result in syndromes with overlapping symptoms?T Edouard, A Montagner, M Dance, et al.
International Journal of Obesity (2005)|January 11, 2014
Impairment of adipose tissue in Prader-Willi syndrome rescued by growth hormone treatmentT Cadoudal, M Buléon, C Sengenès, et al.
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