yves CHAIX
yves CHAIX
UT3 Professor of neuropediatrics, CHU Purpan, Tonic (INSERM-UT3), TMBI (Univ. Toulouse)
Verifierad e-postadress på wibox.fr
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Developmental dyslexia
JF Démonet, MJ Taylor, Y Chaix
The Lancet 363 (9419), 1451-1460, 2004
6602004
Predictors of developmental dyslexia in European orthographies with varying complexity
K Landerl, F Ramus, K Moll, H Lyytinen, PHT Leppänen, K Lohvansuu, ...
Journal of Child Psychology and Psychiatry 54 (6), 686-694, 2013
3412013
Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis
RP de Diego, V Sancho-Shimizu, L Lorenzo, A Puel, S Plancoulaine, ...
Immunity 33 (3), 400-411, 2010
2682010
Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS)
F Pinton, B Ducot, J Motte, AS Arbuès, C Barondiot, MA Barthez, Y Chaix, ...
Epileptic Disorders 8 (1), 11-23, 2006
1712006
Reading abilities and cognitive functions of children with epilepsy: influence of epileptic syndrome
Y Chaix, V Laguitton, V Lauwers-Cances, G Daquin, C Cances, ...
Brain and Development 28 (2), 122-130, 2006
982006
Motor impairment in dyslexia: the influence of attention disorders
Y Chaix, JM Albaret, C Brassard, E Cheuret, P De Castelnau, ...
European Journal of Paediatric Neurology 11 (6), 368-374, 2007
872007
Phonological skills, visual attention span, and visual stress in developmental dyslexia.
A Saksida, S Iannuzzi, C Bogliotti, Y Chaix, JF Démonet, L Bricout, ...
Developmental psychology 52 (10), 1503, 2016
842016
Absence epilepsy with onset before age three years: a heterogeneous and often severe condition
Y Chaix, G Daquin, F Monteiro, N Villeneuve, V Laguitton, P Genton
Epilepsia 44 (7), 944-949, 2003
712003
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
J Becker, D Czamara, TS Scerri, F Ramus, V Csépe, JB Talcott, J Stein, ...
European Journal of Human Genetics 22 (5), 675-680, 2014
622014
Neural signature of DCD: a critical review of MRI neuroimaging studies
M Biotteau, Y Chaix, M Blais, J Tallet, P Péran, JM Albaret
Frontiers in neurology 7, 227, 2016
602016
Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort
G Blanchard, MP Lafforgue, L Lion-François, I Kemlin, D Rodriguez, ...
European Journal of Paediatric Neurology 20 (2), 275-281, 2016
512016
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression
C Mignot, E Apartis, A Durr, CM Lourenço, P Charles, D Devos, C Moreau, ...
Orphanet journal of rare diseases 8 (1), 173, 2013
502013
Behavioural and cognitive phenotypes in children with neurofibromatosis type 1 (NF1): the link with the neurobiological level
C Hachon, S Iannuzzi, Y Chaix
Brain and Development 33 (1), 52-61, 2011
432011
Developmental coordination disorder pertains to a deficit in perceptuo-motor synchronization independent of attentional capacities
P de Castelnau, JM Albaret, Y Chaix, PG Zanone
Human Movement Science 26 (3), 477-490, 2007
432007
Neurofibromatose 1: recommandations de prise en charge
S Pinson, A Créange, S Barbarot, JF Stalder, Y Chaix, D Rodriguez, ...
Archives de pédiatrie 9 (1), 49-60, 2002
37*2002
What do we really know about motor learning in children with Developmental Coordination Disorder?
M Biotteau, Y Chaix, JM Albaret
Current Developmental Disorders Reports 3 (2), 152-160, 2016
362016
Procedural learning and automatization process in children with developmental coordination disorder and/or developmental dyslexia
M Biotteau, Y Chaix, JM Albaret
Human movement science 43, 78-89, 2015
352015
A study of EEG coherence in DCD children during motor synchronization task
P de Castelnau, JM Albaret, Y Chaix, PG Zanone
Human Movement Science 27 (2), 230-241, 2008
342008
Neural changes associated to procedural learning and automatization process in developmental coordination disorder and/or developmental dyslexia
M Biotteau, P Péran, N Vayssière, J Tallet, JM Albaret, Y Chaix
european journal of paediatric neurology 21 (2), 286-299, 2017
292017
Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency
F Sabourdy, L Mourey, E Le Trionnaire, N Bednarek, C Caillaud, Y Chaix, ...
Orphanet journal of rare diseases 10 (1), 31, 2015
272015
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