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Research, science & health

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Discovery of a new gene involved in an early and very severe form of Parkinson's disease
Pr. Alexis Brice's team at the Brain and Spine Institute – Inserm / CNRS / UPMC, in collaboration with two international consortia has identified a new gene, VPS13C, involved in an early form of Parkinson's disease. Mutations in VPS13C lead to a loss...
03.04.2016 Research, science & health
Echange lors d'une conférence
BRAIN BOOSTER AWARDS: our young people are talented
The emergence of multidisciplinary, bold and innovative original research projects carried out by the Institut du Cerveau - ICM’s young talents, thanks to the Bolloré Group support, is the Institut du Cerveau - ICM's Brain Booster Challenge bet.
02.29.2016 Research, science & health
Grégoire Courtine
Invited researcher: Grégoire COURTINE, "motor recovery after spinal cord injury"
Grégoire Courtine is Associate Professor at the Swiss Federal Institute of Technology. He came to the Institut du Cerveau - ICM on February 1, 2016, and presented his research work on the use of new technologies to improve motor recovery after a...
02.15.2016 Research, science & health
Logo Nature Review Neurology
Light cognitive deficit: stem progression toward dementia
In Nature Review Neurology, Professor Harald Hampel and Doctor Simone Lista highlight the need to refine the diagnostic criteria for mild cognitive impairment (MCI) in order to set preventive measures and stem the progression toward dementia in...
05.11.2016 Research, science & health
bassem hassan
Bassem Hassan joins Paris Brain Institute
Paris Brain Institute brings together in one place patients, doctors and researchers in order to rapidly develop treatments for nerve damage and apply these to patients as soon as possible. Coming from all backgrounds and countries, the best...
01.29.2016 Research, science & health
Bassem Hassan
Brain development: Discovery of a new regulatory mechanism
Bassem Hassan’s team at VIB/KU Leuven has discovered a previously unknown mechanism that is highly conserved between species and which regulates neurogenesis through precise temporal control of the activity of a family of proteins essential for brain...
02.11.2016 Research, science & health
image
Dementia or Alzheimer's : a simple test could differentiate them
Patients with fronto-temporal dementia need specific and appropriate medical care. However, this disease is still too often confused with Alzheimer's disease. Clinicians and researchers from Paris Brain Institute and from the Memory and Alzheimer's...
01.22.2016 Research, science & health
Fiona Doetsch
Invited researcher: Fiona DOETSCH, "stem cells and neurodegenerative diseases"
Fiona Doetsch is a research group leader at the Biozentrum of the University of Basel. Upon her visit at the Institut du Cerveau - ICM, she presented her work on stem cells, and more specifically, on what triggers their activation. Stem cells could...
01.04.2016 Research, science & health
Maladie de Parkinson : un mécanisme qui protège les neurones
Parkinson's disease: a neuronal protective mechanism
The Institut du Cerveau - ICM scientists have recently discovered a mechanism which protects neurons from cell death. The loss of this protective mechanism may contribute to the degeneration of neurons in patients with Parkinson's disease.
12.23.2015 Research, science & health
prions
Prion diseases: a model for neurodegenerative disorders
The majority of neurodegenerative disorders, from Alzheimer's disease to amyotrophic lateral sclerosis to Parkinson's disease, share common features with prion diseases.
12.09.2015 Research, science & health
Journée mondiale de l’épilepsie
National epilepsy day: research at the ICM
On the occasion of National Epilepsy Day, Vincent Navarro, neurologist and Institut du Cerveau - ICM researcher, and Stéphanie Baulac, co-leader of the team “Genetics and physiology of hereditary epilepsy,” and the start-up Bioserenity led a...
11.27.2015 Research, science & health
Visualisation de l'ADN
Hereditary spastic paraplegia: discovery of a new mechanism
A team at the Institut du Cerveau - ICM showed that different mutations of one gene, ALDH18A1, are associated with several types of hereditary spastic paraplegias and different modes of transmission. Moreover, the researchers identified a new blood...
11.24.2015 Research, science & health