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Neuropsychological and neuroanatomical phenotype in 17 patients with cystinosis
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In: Orphanet journal of rare diseases ; https://hal.archives-ouvertes.fr/hal-02901744 ; Orphanet journal of rare diseases, 2020, 15 (1), pp.59. ⟨10.1186/s13023-019-1271-6⟩ (2020)
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New insight in ARX-mutated patients' language specific impairment and underlying FOXP1 dysregulation
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In: ISSN: 1090-3798 ; European Journal of Paediatric Neurology ; https://hal.archives-ouvertes.fr/hal-02871228 ; European Journal of Paediatric Neurology, Elsevier, 2017, 21, pp.e66. ⟨10.1016/j.ejpn.2017.04.936⟩ (2017)
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