Filter your results
- 3
- 3
- 3
- 2
- 1
- 3
- 3
- 3
- 2
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
|
|
sorted by
|
Reading impairment in an adolescent with temporo-occipital epilepsy. Pre- and post-surgical evaluationNeurocase, 2014, 20 (1), pp.87--99. ⟨10.1080/13554794.2012.732088⟩
Journal articles
hal-01064634v1
|
|||
|
Mosaic parental germline mutations causing recurrent forms of malformations of cortical developmentEuropean Journal of Human Genetics, 2016, 24 (4), pp.611--614. ⟨10.1038/ejhg.2015.192⟩
Journal articles
hal-01313739v1
|
||
|
Epilepsy in young Tsc1+/− mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complexEpilepsia, 2016, 57 (4), pp.648-659. ⟨10.1111/epi.13325⟩
Journal articles
hal-01274304v1
|