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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 2 of 2 1 Neuropsychological and neuroanatomical phenotype in 17 patients with cystinosis Curie, A.; Touil, N.; Gaillard, S.... 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) BASE Show details 2 New insight in ARX-mutated patients' language specific impairment and underlying FOXP1 dysregulation Curie, A.; Friocourt, G.; Bertrand, S.... 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) BASE Show details

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