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Pediatrie|June 1, 1984
[Byler's disease. Ultrastructural study. Apropos of a case in an infant]J A Pincon, P Chatelain, Y Mallet-Guy, et al.
Nephron|April 5, 2001
Inheritance of a stable mutation in a family with early-onset diseaseR A Perrichot, B Mercier, L de Parscau, et al.
Metabolism: Clinical and Experimental|July 1, 1986
Antiketogenic effect of glucose per se in vivo in man and in vitro in isolated rat liver cellsJ P Riou, M Beylot, M Laville, et al.
Pediatrie|January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]L de Parscau, B Beaufrère, C Vianey-Liaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 28, 2002
[Nosocomial infections due to human coronaviruses in the newborn]A Gagneur, M C Legrand, B Picard, et al.
Early Human Development|October 20, 2001
Neonatal screening and long-term follow-up of phenylketonuria: the French databaseV Abadie, J Berthelot, F Feillet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2005
[Management of phenylketonuria and hyperphenylalaninemia: the French guidelines]V Abadie, J Berthelot, F Feillet, et al.
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