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Results:
1-8
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Results: 8
Authors:
Lyon, G
Citation: G. Lyon, Comparison of two code scalability tests, INF PROCESS, 81(3), 2002, pp. 169-174
Authors:
Huryn, AD
Riley, RH
Young, RG
Arbuckle, CJ
Peacock, K
Lyon, G
Citation: Ad. Huryn et al., Temporal shift in contribution of terrestrial organic matter to consumer production in a grassland river, FRESHW BIOL, 46(2), 2001, pp. 213-226
Authors:
Imessaoudene, B
Bonnefont, JP
Royer, G
Cormier-Daire, V
Lyonnet, S
Lyon, G
Munnich, A
Amiel, J
Citation: B. Imessaoudene et al., MECP2 mutation in non-fatal, non-progressive encephalopathy in a male, J MED GENET, 38(3), 2001, pp. 171-174
Authors:
Amouyel, P
Farnier, M
Lyon, G
Siest, G
Mortier, N
Amiot, N
Duprat-Lomon, I
Citation: P. Amouyel et al., Management of dyslipidaemia diagnosed in general practice in France - The PRAGMA study, ARCH MAL C, 94(10), 2001, pp. 1045-1053
Authors:
Lyon, G
Stephan, G
Citation: G. Lyon et G. Stephan, Forms of discontent (An interview with Gary Stephan), PAJ, (66), 2000, pp. 19-37
Authors:
Papadopoulou, LC
Sue, CM
Davidson, MM
Tanji, K
Nishino, I
Sadlock, JE
Krishna, S
Walker, W
Selby, J
Glerum, DM
Van Coster, R
Lyon, G
Scalais, E
Lebel, R
Kaplan, P
Shanske, S
De Vivo, DC
Bonilla, E
Hirano, M
DiMauro, S
Schon, EA
Citation: Lc. Papadopoulou et al., Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene, NAT GENET, 23(3), 1999, pp. 333-337
Authors:
Lyon, G
Citation: G. Lyon, Language and perceptual experience, PHILOSOPHY, 74(290), 1999, pp. 515-534
Authors:
Leuzzi, V
Lyon, G
Cilio, MR
Pedespan, JM
Fontan, D
Chateil, JF
Vital, A
Citation: V. Leuzzi et al., Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases, J NE NE PSY, 66(3), 1999, pp. 407-408
Risultati:
1-8
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