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Agnès Rastetter. Assistante ingénieur chez ICM - Brain & Spine Institute. Lieu Région de Paris , France Secteur Biotechnologie
Interests
Genetic and neurodevelopmental spectrum of SYNGAP1-associated...
jmg.bmj.com
Agnès Rastetter 6, Benoit Gachet 6, Yannick Marie 6, G Christoph Korenke 11, Ingo Borggraefe 12, ...
Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor...
www.cell.com
Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium ,. Agnès Rastetter. x. Agnès Rastetter.
Education
De novo mutations in HCN1 cause early infantile epileptic...
kclpure.kcl.ac.uk
De novo mutations in HCN1 cause early infantile epileptic encephalopathy Agnès Rastetter ; Pasquale Striano ; Carolien G F de Kovel ; Rima Nabbout ; ...
Bad news
Heritage
Marlis-Rastetter - User Trees - Genealogy.com
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Family Tree Maker user home page for Marlis-Rastetter.
Scientific Publications
Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor...
www.sciencedirect.com
Agnès Rastetter 1, 2, 3, 4, Amir Boukhris Alteration of fatty-…-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.
Annonacin, a natural lipophilic mitochondrial complex I inhibitor,...
www.sciencedirect.com
Matthias Höllerhage a,c,d, Christel Depienne e, Agnès Rastetter e, Agathe Tarze f, Bertrand Friguet g,. Mohamed Salama a, Pierre Champy h, ...
Publications
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A...
www.oalib.com
SHANK genes code for scaffold proteins located at the post-synaptic density of glutamatergic synapses. In neurons, SHANK2 and SHANK3 have a positive effect on...
Hypomorphic variants of cationic amino … transporter 3 in males...
link.springer.com
... Agnès Rastetter (1) (2) (3) (4); Claire Amiet (10); Aurélia Jacquette (5) (7) (8); Céline Dupuits (1) (2) (3) (4); Delphine Bouteiller (1) (2) (3) (4); Boris Keren (5) ...
Guilmatre A, Huguet G, Delorme R, …
www.oalib.com
... Rappold,Richard Holt,Anthony P. Monaco,Elena Maestrini,Pilar Galan,Delphine Heron,Aurélia Jacquette,Alexandra Afenjar,Agnès Rastetter,Alexis Brice,Fran？
Reports & Statements
De novo mutations in HCN1 cause early infantile epileptic...
www.nature.com
Christel Depienne, Eric LeGuern and colleagues report the identification of 5 de novo missense mutations in HCN1 in individuals with early-onset epileptic...
Current and past members of the team | The EPHE Neurogenetics Team
epheneurogeneticsteam.wordpress.com
Staff members Current team Previous members
Miscellaneous
Agnès Rastetter | LinkedIn
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Agnès Rastetter
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Agnès Rastetter. Details · Publications ... Elodie Martin, Constantin Yanicostas, Agnès Rastetter, Seyedeh Maryam Alavi Naini, more · Neurobiology of Disease ...
Annonacin, a natural lipophilic mitochondrial complex I inhibitor,...
www.hal.inserm.fr
Christel Depienne 5 Agnès Rastetter 5 Agathe Tarze 6 Bertrand Friguet 7 Mohamed Salama 1 Pierre Champy 8 Wolfgang Oertel 1 Günter Höglinger 1, 3, 4, ...
SpringerCitations - Details Page
citations.springernature.com
Elodie Martin, Rebecca Schüle, Katrien Smets, Agnès Rastetter, Amir Boukhris, José L. Loureiro, Michael A. Gonzalez, Emeline Mundwiller, Tine Deconinck, ...
Agnes Rastetter Marlis (living trust) | Manor Lane, Concord, CA...
blockshopper.com
N/A, ResaleB: Marlis Agnes Rastetter (Living Trust), Rastetter Marlis A (Trustee), BA: N/A. S: Marlis Odegaard Rastetter Revoc (Living Trust), ...
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A...
journals.plos.org
Agnès Rastetter, Affiliations: INSERM U CRICM, Institut du cerveau et de la moelle épinière (ICM), CNRS CRICM, Hôpital ...
…-responsive basal ganglia disease in ethnic Europeans with...
hal.sorbonne-universite.fr
OBJECTIVE: To report the first 2 European cases of …-responsive basal ganglia disease and novel SLC19A3 mutations. DESIGN: Case reports. SETTING:...
…-responsive basal ganglia disease in ethnic Europeans with...
Rabab Debs, Christel Depienne, Agnès Rastetter, Agnès Bellanger, Bertrand Degos, Damien Galanaud, Boris Keren, Olivier Lyon-Caen, Alexis Brice, Frédéric ...
Cellular distribution and subcellular localization of spatacsin and...
read.qxmd.com
Reena Prity Murmu, Elodie Martin, Agnès Rastetter, Typhaine Esteves, Marie-Paule Muriel, Khalid Hamid El Hachimi, Paola Silvia Denora, Aurélien Dauphin, ...
iGenSeq : genotyping and sequencing core facility - Institut du...
institutducerveau-icm.org
iGenSeq : genotyping and sequencing core facility. Imprimer. iGenSeq provides tools and services for genome analysis to academics or industrials Agnès Rastetter ...
De novo mutations in HCN1 cause early infantile epileptic...
researchportal.helsinki.fi
Caroline Nava ; Carine Dalle ; Agnes Rastetter ; Pasquale Striano ; Carolien G. F. de Kovel ; Rima Nabbout ; Claude Cances ; Dorothee Ville ; Eva H. Brilstra ...
Une avancée majeure dans la compréhension des épilepsies sévères -...
institutducerveau-icm.org
Agnès Rastetter, Christel Depienne, Caroline Nava et Carine Dalle. Imprimer. ICM - Hôpital Pitié Salpêtrière. 47, bd de l'hôpital PARIS - France. Plan d
PLOS Genetics: Publishing science, accelerating research
journals.plos.org
... Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiesa, ...
Papers in the journal Nature Genetics | Read by QxMD
54.83.30.70
Caroline Nava, Carine Dalle, Agnès Rastetter, Pasquale Striano, Carolien G F de Kovel, Rima Nabbout, Claude Cancès, Dorothée Ville, Eva H Brilstra, ...
- oalib
www.jourlib.org
... Heron,Aurélia Jacquette,Alexandra Afenjar,Agnès Rastetter,Alexis Brice,Fran？oise Devillard,Brigitte Assouline,Fanny Laffargue,James ...
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