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	1.	[Radiology clinical case]. [electronic resource] by Lagrue, E Martinerie, L Adamsbaum, C Producer: 20040106 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Basal ganglia neuroprotection with anticonvulsants after energy stress: a comparative study. [electronic resource] by Arpin, S Lagrue, E Bodard, S Chalon, S Castelnau, P Producer: 20091230 In: Metabolic brain disease vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Newborn asphyxia at term during delivery]. [electronic resource] by Lodé, N Chabernaud, J-L Chouakri, O Casadevall, I Maury, I Lagrue, E Lavaud, J Producer: 20030404 In: Journal de gynecologie, obstetrique et biologie de la reproduction vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	4.	[N-methyl-D-aspartate receptor antibody encephalitis: value of immunomodulatory therapy]. [electronic resource] by Le Moigno, L Ternant, D Paintaud, G Thibault, G Cloarec, S Tardieu, M Lagrue, E Castelnau, P Producer: 20150106 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood. [electronic resource] by Lagrue, E Abert, B Nadal, L Tabone, L Bodard, S Medja, F Lombes, A Chalon, S Castelnau, P Producer: 20090914 In: Metabolic brain disease vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia. [electronic resource] by Furby, A Vicart, S Camdessanché, J P Fournier, E Chabrier, S Lagrue, E Paricio, C Blondy, P Touraine, R Sternberg, D Fontaine, B Producer: 20150720 In: Neuromuscular disorders : NMD vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters. [electronic resource] by Uettwiller, F Sarrabay, G Rodero, M P Rice, G I Lagrue, E Marot, Y Deiva, K Touitou, I Crow, Y J Quartier, P Producer: 20160602 In: RMD open vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)