
Institut du Cerveau
Articles
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Nov 13, 2024 |
jamanetwork.com | Hugo Bottemanne |Assistance Publique |Institut du Cerveau |Lucie Joly
How the Paternal Brain Is Wired by Pregnancy Pregnancy and post partum are accompanied by structural and functional brain changes in women that are thought to be important for caregiving.1 Studies have shown that pregnancy in women is associated with extensive gray matter volume reductions during pregnancy.1 Compared with controls, expecting mothers present lower cortical volume across several brain areas, with fewer cortical differences in the early postpartum period.1 Some of these brain...
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Oct 26, 2024 |
onlinelibrary.wiley.com | Eva H. Brilstra |Floor Jansen |Sara Baldassari |Institut du Cerveau
1 INTRODUCTION Epilepsy surgery is the most effective treatment in epilepsy patients who develop refractory seizures, provided that the epileptogenic zone is focal, well delineated, preferably of presumed structural origin, and outside eloquent areas.1 Genetic malformations of cortical development (MCD), such as mild MCD (mMCD), mMCD with oligodendroglial hyperplasia and epilepsy (MOGHE), focal cortical dysplasia (FCD; especially FCDIIa and FCDIIb subtypes), and hemimegalencephaly (HMEG)...
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Oct 19, 2024 |
movementdisorders.onlinelibrary.wiley.com | Emmanuel Roze |Institut du Cerveau |AP-HP Paris France
The Ultragenyx@-sponsored phase 3 randomized controlled study evaluating the effect of triheptanoin to treat paroxysmal episodes of movement disorders related to Glut1 deficiency syndrome (Glut1-DS) failed to demonstrate efficacy.1 This was unexpected considering the rationale supporting the use of triheptanoin,2 and the striking results of preliminary investigator-driven open-label studies that showed over 90% reduction of paroxysmal movement disorders in patients with Glut1-DS,3, 4 a...
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Oct 8, 2024 |
academic.oup.com | Institut du Cerveau |Movement Neurosciences
Spinocerebellar ataxia 27B (SCA27B) is a common autosomal dominant ataxia caused by an intronic GAA•TTC repeat expansion in FGF14. Neuropathological studies have shown that neuronal loss is largely restricted to the cerebellum. Although the repeat locus is highly unstable during intergenerational transmission, it remains unknown whether it exhibits cerebral mosaicism and progressive instability throughout life.
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Sep 23, 2024 |
movementdisorders.onlinelibrary.wiley.com | Guillaume Cogan |Institut du Cerveau |Christelle Tesson
More than a dozen genes are involved in monogenic forms of Parkinson's disease (PD).1 Their discovery have contributed to our understanding of the biology of PD and highlighted the role of α-synuclein, mitochondrial homeostasis, vesicle trafficking, endolysosomal system, and other pathways in PD.2 However, they explain only less than 10% of PD cases, suggesting that more genes are still to be identified.
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