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[Neonatal detection of central hypothyroidism].
Giroux B, Metz C, Giroux JD, de Parscau L. Giroux B, et al. Among authors: de parscau l. Arch Pediatr. 1997 Jun;4(6):542-6. doi: 10.1016/s0929-693x(97)87576-8. Arch Pediatr. 1997. PMID: 9239270 French.
Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.
Teissier R, Nowak E, Assoun M, Mention K, Cano A, Fouilhoux A, Feillet F, Ogier H, Oger E, de Parscau L; AFDPHE (Association Française pour le Dépistage et la Prévention des Handicaps de l’Enfant). Teissier R, et al. Among authors: de parscau l. J Inherit Metab Dis. 2012 Nov;35(6):993-9. doi: 10.1007/s10545-012-9491-0. Epub 2012 Jun 5. J Inherit Metab Dis. 2012. PMID: 22669364
[Neonatal diabetes mellitus associated with an autoimmune disease].
Finel E, Giroux JD, Metz C, Robert JJ, Robert O, Sadoun E, Alix D, de Parscau L. Finel E, et al. Among authors: de parscau l. Arch Pediatr. 1996 Aug;3(8):782-4. doi: 10.1016/0929-693x(96)82160-9. Arch Pediatr. 1996. PMID: 8998531 French.
[Management of phenylketonuria and hyperphenylalaninemia: the French guidelines].
Abadie V, Berthelot J, Feillet F, Maurin N, Mercier A, Ogier de Baulny H, de Parscau L; Association française pour le dépistage et la prévention des handicaps de l'enfant (AFDPHE). Abadie V, et al. Among authors: de parscau l. Arch Pediatr. 2005 May;12(5):594-601. doi: 10.1016/j.arcped.2005.02.004. Arch Pediatr. 2005. PMID: 15885553 Review. French.
109 results