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The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients.
Orphanet J Rare Dis. 2012 Oct 9;7:77. doi: 10.1186/1750-1172-7-77.
Orphanet J Rare Dis. 2012.
PMID: 23046562
Free PMC article.
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management].
Feillet F, Ogier H, Cheillan D, Aquaviva C, Labarthe F, Baruteau J, Chabrol B, de Lonlay P, Valayanopoulos V, Garnotel R, Dobbelaere D, Briand G, Jeannesson E, Vassault A, Vianey-Saban C; SFEIM (Société française pour l’étude des erreurs innées du métabolisme).
Feillet F, et al. Among authors: valayanopoulos v.
Arch Pediatr. 2012 Feb;19(2):184-93. doi: 10.1016/j.arcped.2011.10.025. Epub 2012 Jan 12.
Arch Pediatr. 2012.
PMID: 22244319
French.
Item in Clipboard
[Neonatal epilepsy and inborn errors of metabolism].
Bahi-Buisson N, Mention K, Léger PL, Valayanopoulos V, Nabbout R, Kaminska A, Plouin P, Dulac O, de Lonlay P, Desguerre I.
Bahi-Buisson N, et al. Among authors: valayanopoulos v.
Arch Pediatr. 2006 Mar;13(3):284-92. doi: 10.1016/j.arcped.2005.10.024. Epub 2005 Dec 15.
Arch Pediatr. 2006.
PMID: 16343871
Review.
French.
Item in Clipboard
[Radiological innovations in the screening and diagnosis of the inborn errors of metabolism].
Boddaert N, Ribeiro M, Touati G, Mention K, Valayanopoulos V, Nihoul-Fékété C, Brunelle F, de Lonlay P.
Boddaert N, et al. Among authors: valayanopoulos v.
Med Sci (Paris). 2005 Nov;21(11):981-6. doi: 10.1051/medsci/20052111981.
Med Sci (Paris). 2005.
PMID: 16274650
Free article.
Review.
French.
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