Neurosciences
Cerebellar Malformations
SCA42ND iPSCs
Brain organoïds
DNA samples from patients with Early-onset cerebellar atrophy
>40 patient cohort
Dysphasies
> 15 patients
>15 patient cohort
Dystonia and movement disorders
Aprepitant for use in the topical treatment of facial neuralgia
Patient cohort
Malformation of cortical development
Team
Neurodegeneration
Brain organoïds (AD)
Brain organoïds (PD)
DNA from patients with Friedreich ataxia
Fibroblasts from patients with Freidreich ataxia
> 200 patients (pediatric and adult)
Treatment and prediction of therapeutic responses in patients suffering from Friedreich ataxia
Novel serotonin analogues and their uses for treating iron-associated disorders
NCT04921930 – Evaluation of the Effect of Artesunate in Friedreich Ataxia (FA)
NCT05874388 – Characterisation of the Cognitive Profile of Patients Suffering From Friedreich’s Ataxia
Neurodevelopmental Disorders
Patient cohort
Patient cohort
> 200 patient cohort
Patient cohort
>50 atient cohort
NCT04259281 – A Study of the Safety and Tolerability of GTX-102 in Children With Angelman Syndrome
NCT05127226 – HALOS: A Safety Tolerability Pharmacokinetics and Pharmacodynamics Study of Multiple Ascending Doses of ION582 in Participants With Angelman Syndrome
NCT05630066 – Study to Investigate the Pharmacokinetics and Safety and to Provide Proof of Mechanism of Alogabat in Children and Adolescents Aged 5-17 Years With Angelman Syndrome (AS) With Deletion Genotype.
Transcranial magnetic stimulation protocol
>300 patient cohort
NCT04607616 – Interactive Guidance Therapy With Video Feed-back of Parent and Child With Autism Spectrum Disorder
NCT04442061 – Autism Spectrum Disorders: Double Blind Randomized Placebo-control Active Pilot Study of Transcranial Magnetic Stimulation Applied to the Superior Temporal Sulcus
NCT05271955 – e-GOLIAH in Autistic Spectrum Disorders
Patient cohort
Team
Neurometabolic Disorders
Cerebellum specific Srd5a3 KO mice
Rare Epilepsies
>50 patient cohort
>30 patient cohort
NCT05163314 – A Study of Soticlestat as an Add-on Therapy in Children and Adults With Dravet Syndrome or Lennox-Gastaut Syndrome
NCT05772429 – Long-term Follow-up of a Multicentre Non-interventional Prospective Cohort of Participants Prescribed Epidyolex in France in a Real-life Setting (OPERA)
NCT04938427 – A Study of Soticlestat as an Add-on Therapy in Children Teenagers and Adults With Lennox-Gastaut Syndrome
>15 patient cohort
Patient cohort
>15 patient cohort
>35 patient cohort
Patient cohort
>10 patients cohort
>15 patient cohort
Patient cohort
> 120 patient cohort
NCT04940624 – A Study of Soticlestat as an Add-on Therapy in Children and Young Adults With Dravet Syndrome
NCT05163314 – A Study of Soticlestat as an Add-on Therapy in Children and Adults With Dravet Syndrome or Lennox-Gastaut Syndrome
NCT05772429 – Long-term Follow-up of a Multicentre Non-interventional Prospective Cohort of Participants Prescribed Epidyolex in France in a Real-life Setting (OPERA)
> 50 patient cohort
Spinal Cord Disorders
Patient cohort
Patient cohort
Team
Congenital and infantile glaucomas
Neuroinflammation
Cell lines from patients with AGS
EBV-B
HEK cell line
HELA cell line
Singe-cell transcriptomics – CITE-seq protocol – Network inference analysis
THP1 cell line
>100 patients (mainly pediatric)
Fibroblasts from patients
IFNa IFNb dosage in patients’ cells supernatants – IFN signature – pSTAT3 and STING intracellular staining – pTBK1 elisa test – Apoptosis evaluation – T-reg suppression analysis -Phenotyping of T-reg CD4-/CD8- – Single-cell transcriptomics – CITE-seq protocol – Network inference analysis
iPSC from patients
PBMCs from patients
STING-KI mice (V154M CRISPR/Cas9)
20 patients (mainly pediatric)
Neuronal Ciliopathies
Team
Iron homeostasis
Fibroblasts from patients with NBIA
Fibroblasts from patients with NBIA
> 10 patient cohort