10 results on '"Boddaert, Nathalie"'
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2. Further refinement of COL4A1 and COL4A2 related cortical malformations
3. Mutations in TBR1 gene leads to cortical malformations and intellectual disability
4. TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly
5. From splitting GLUT1 deficiency syndromes to overlapping phenotypes
6. Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysis
7. Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family
8. Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiency
9. Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction
10. Early epileptic encephalopathies associated with STXBP1 mutations: Could we better delineate the phenotype?
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