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des Portes, V
147
results:
Search for persons
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Format
Online (146)
Print (1)
Mediatypes
Articles (Online) (96)
Articles (Print) (1)
OpenAccess-fulltext (50)
Languages
english (108)
french (30)
Sorted by: Relevance
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?
1
STAG2 microduplication in a patient with eyelid myoclonia a..:
Gokce-Samar, Z.
;
de Bellescize, J.
;
Arzimanoglou, A.
...
European Journal of Medical Genetics. 65 (2022) 12 - p. 104636 , 2022
Link:
https://doi.org/10.1016/..
?
2
A french adaptation of the vineland adaptive behavior scale..:
Touil, N.
;
Riche, B.
;
Portes, V. Des
...
European Psychiatry. 64 (2021) S1 - p. S155-S156 , 2021
Link:
https://doi.org/10.1192/..
?
3
Spatial distribution of Brazilian bovine taurine breeds ass..:
Alfonzo, E.P.M.
;
McManus, C.M.
;
Campos, G.S.
...
Arquivo Brasileiro de Medicina Veterinária e Zootecnia. 73 (2021) 3 - p. 693-702 , 2021
Link:
https://doi.org/10.1590/..
?
4
Role of multidimensional evaluations in the support of scho..:
Touil, N.
;
Curie, A.
;
Reymond, M.-P.
...
European Psychiatry. 64 (2021) S1 - p. S125-S126 , 2021
Link:
https://doi.org/10.1192/..
?
5
Corpus callosum agenesis with clinically normal people caus..:
Billette de Villemeur, T.
;
Valence, S.
;
Heron, D.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e43 , 2017
Link:
https://doi.org/10.1016/..
?
6
New insight in ARX-mutated patients' language specific impa..:
Curie, A.
;
Friocourt, G.
;
Bertrand, S.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e66 , 2017
Link:
https://doi.org/10.1016/..
?
7
West syndrome due to compound heterozygous QARS mutations:
Poulat, A.L.
;
Lesca, G.
;
Chatron, N.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e99 , 2017
Link:
https://doi.org/10.1016/..
?
8
Christianson syndrome: An underestimated cause of electrica..:
Mathieu, M.-L.
;
de Bellescize, J.
;
Till, M.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e98 , 2017
Link:
https://doi.org/10.1016/..
?
9
Developmental trajectories of 31 French Creatine Transporte..:
Lion-François, L.
;
Valayannopoulos, V.
;
Perreton, N.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e64-e65 , 2017
Link:
https://doi.org/10.1016/..
?
10
Next-generation sequencing allows a diagnostic yield of 23...:
Lesca, G.
;
Labalme, A.
;
Mignot, C.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e168-e169 , 2017
Link:
https://doi.org/10.1016/..
?
11
Anti-tumor necrosis factor alpha therapy, Adalimumab, in Ra..:
Villeneuve, N.
;
Lagarde, S.
;
Lepine, A.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e8 , 2017
Link:
https://doi.org/10.1016/..
?
12
6q22.1 deletion is associated with epilepsy and abnormal mo..:
Schluth-Bolard, C.
;
Flamand-Roze, E.
;
Masurel, A.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e52-e53 , 2017
Link:
https://doi.org/10.1016/..
?
13
Severe cognitive impairment and early-onset epilepsy in six..:
Chatron, N.
;
Møller, R.S.
;
Champaigne, N.L.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e194 , 2017
Link:
https://doi.org/10.1016/..
?
14
Basal ganglia involvement in ARX gene mutated patients: The..:
Curie, A.
;
Friocourt, G.
;
des Portes, V.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e62 , 2017
Link:
https://doi.org/10.1016/..
?
15
Next-generation sequencing (NGS) is a powerful tool to impr..:
Labalme, A.
;
Chatron, N.
;
Till, M.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e52 , 2017
Link:
https://doi.org/10.1016/..
1-15