A. Curie

发表

Neural correlates of non-verbal social interactions: A dual-EEG study

Y. Paulignan, T. Nazir, Anne Cheylus, 2014, Neuropsychologia.

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome

Mark F. Bear, Eva Loth, Jacqueline N. Crawley, 2017, Nature Reviews Drug Discovery.

Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiency.

M. Zilbovicius, N. Boddaert, S. Chanraud, 2009, European journal of medical genetics.

Syntax at Hand: Common Syntactic Structures for Actions and Language

Viviane Deprez, Alice C. Roy, Yves Paulignan, 2013, PloS one.

Motor resonance facilitates movement execution: an ERP and kinematic study

Y. Paulignan, T. Nazir, V. des Portes, 2013, Front. Hum. Neurosci..

Simultaneous action execution and observation optimise grasping actions

Y. Paulignan, T. Nazir, M. Ménoret, 2013, Experimental Brain Research.

Outcome of isolated agenesis of the corpus callosum: A population-based prospective study.

F. Rivier, D. Ville, V. des Portes, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Sébastien Jacquemont Associated with Differential Response to the mGluR 5 Antagonist AFQ 056 Gene in Fragile X Syndrome Is FMR 1 Epigenetic Modification of the

J. Beckmann, N. Hadjikhani, Joanne M. Meyer, 2010 .

Deciphering the natural history of SCA7 in children

A. Durr, D. Devos, C. Cazeneuve, 2020, European journal of neurology.

Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with SLC16A2 mutations

R. Touraine, D. Rodriguez, O. Boespflug-Tanguy, 2019, Developmental medicine and child neurology.

Antagonism of mGluR5 in Fragile X: A Randomized, Placebo-Controlled, Proof-of-Concept Study of AFQ056, a Novel, Sub-Type Selective mGluR5 Antagonist

J. Beckmann, N. Hadjikhani, Joanne M. Meyer, 2011 .

Stroke by carotid artery complete occlusion in Kawasaki disease: case report and review of literature.

N. Hadjikhani, R. Gollub, J. Kong, 2013, Pediatric neurology.

Simultaneous action execution and observation optimise grasping actions

Y. Paulignan, T. Nazir, M. Ménoret, 2013, Experimental Brain Research.

Placebo Responses in Genetically Determined Intellectual Disability: A Meta-Analysis

R. Gollub, I. Kirsch, T. Kaptchuk, 2015, PloS one.

Neuropsychological and neuroanatomical phenotype in 17 patients with cystinosis

D. Galanaud, J. Luauté, F. Cotton, 2020, Orphanet Journal of Rare Diseases.

Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

Janice Branson, Jacques S. Beckmann, Nouchine Hadjikhani, 2011, Science Translational Medicine.

Pathogenic TRIO variants associated with neurodevelopmental disorders perturb the molecular regulation of TRIO and axon pathfinding in vivo

D. Baralle, A. Debant, S. Schmidt, 2023, Molecular Psychiatry.

Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all cases.

V. Cottin, G. Bellon, A. Curie, 2007, The Journal of pediatrics.

A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome

N. Philip, J. Mandel, J. Thevenon, 2016, American journal of medical genetics. Part A.

The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1‐mutated males

L. Hertz-Pannier, R. Touraine, F. Giuliano, 2011, Clinical genetics.

Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant

V. des Portes, A. Curie, A. Calender, 2017, Psychiatric genetics.

The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia

Alice C. Roy, Y. Paulignan, T. Nazir, 2014, Orphanet Journal of Rare Diseases.

Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?

Alice C. Roy, Y. Paulignan, T. Nazir, 2018, NeuroImage: Clinical.

Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification

Jean-Francois Mangin, David Germanaud, Julien Lefèvre, 2014, NeuroImage.

A new mouse model of ARX dup24 recapitulates the patients’ behavioral and fine motor alterations

Y. Hérault, T. Sorg, Y. Humeau, 2018, Human molecular genetics.

Implicit procedural learning in fragile X and Down syndrome.

V. des Portes, A. Curie, G. Bussy, 2011, Journal of intellectual disability research : JIDR.

A Novel Analog Reasoning Paradigm: New Insights in Intellectually Disabled Patients

Y. Paulignan, T. Nazir, N. Hadjikhani, 2016, PloS one.

Placebo effects in children with autism spectrum disorder

T. Oberlander, A. Curie, K. Jensen, 2023, Developmental medicine and child neurology.

Epigenetic modification of the FMR1 gene in fragile X patients leads to a differential response to the mGluR5 antagonist AFQ056

F. Ramos, E. Berry-Kravis, M. Torrioli, 2011 .

Certainty of genuine treatment increases drug responses among intellectually disabled patients

R. Gollub, I. Kirsch, T. Kaptchuk, 2017, Neurology.

Implicit procedural learning in fragile X and Down syndrome.

A. Curie, V. Portes, G. Bussy, 2011, Journal of intellectual disability research : JIDR.

Clinical Characteristics, Developmental Trajectory, and Caregiver Burden of Patients With Creatine Transporter Deficiency (SLC6A8).

A. Curie, B. Kassai, V. Valayannopoulos, 2024, Neurology.