Oxytocin receptor agonist reduces perinatal brain damage by targeting microglia
Jérôme Mairesse
,
Manuela Zinni
,
Julien Pansiot
,
Rahma Hassan-Abdi
,
Charlie Demené
,
et al.
Journal articles
inserm-04075780v1
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Severe respiratory complex III defect prevents liver adaptation to prolonged fasting
Laura S Kremer
,
Caroline L 'Hermitte-Stead
,
Pierre Lesimple
,
Mylène Gilleron
,
Sandrine Filaut
,
et al.
Journal articles
inserm-01321215v1
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[Vaccine encephalopathy: a myth collapses?]
Philippe Kahane
,
Alexis Arzimanoglou
Journal articles
inserm-00410857v1
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Nocturnal hypermotor seizures, suggesting frontal lobe epilepsy, can originate in the insula.
Philippe Ryvlin
,
Lorella Minotti
,
Geneviève Demarquay
,
Edouard Hirsch
,
Alexis Arzimanoglou
,
et al.
Journal articles
inserm-00388334v1
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Ethical management in the constitution of a European database for leukodystrophies rare diseases.
Nathalie Duchange
,
Sylviane Darquy
,
Diane d'Audiffret
,
Ingrid Callies
,
Anne-Sophie Lapointe
,
et al.
Journal articles
inserm-00995366v1
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Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation
Imen Dorboz
,
Hélène Dumay-Odelot
,
Karima Boussaid
,
Yosra Bouyacoub
,
Pauline Barreau
,
et al.
Journal articles
pasteur-02000258v1
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Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains
Nina Dupuis
,
Andrey Mazarati
,
Béatrice Desnous
,
Vibol Chhor
,
Bobbi Fleiss
,
et al.
Journal articles
inserm-01415098v1
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Grande prématurité : dépistage et prévention du risque
Michel Dehan
,
Philippe Evrard
,
Françoise Ferre
,
Monique Kaminski
,
Jacques de Mouzon
,
et al.
[Rapport de recherche] Institut national de la santé et de la recherche médicale(INSERM). 1997, 246 p., figures, tableaux, graphiques, références bibliographiques disséminées
Reports
hal-01570660v1
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[Medicoeconomic assessment of epilepsy surgery in adults with medically intractable partial epilepsy. Three-year outcomes from a multicenter French cohort]
Marie-Christine Picot
,
Audrey Jaussent
,
Philippe Kahane
,
Arielle Crespel
,
Philippe Gélisse
,
et al.
Journal articles
inserm-00410612v1
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Towards a definition of the "practical" epileptogenic zone: a case of epilepsy with dual pathology.
Serge Chassagnon
,
Maria Paola Valenti
,
Cécile Sabourdy
,
Philippe Esposito
,
Pierre Kehrli
,
et al.
Epileptic Disorders , 2006, 8 Suppl 2, pp.S67-76
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inserm-00388238v1
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Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells
Paule Bénit
,
Agathe Kahn
,
Dominique Chretien
,
Sylvie Bortoli
,
Laurence Huc
,
et al.
Journal articles
inserm-02409310v1
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Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations.
Serena Grossi
,
Stefano Regis
,
Roberta Biancheri
,
Matthew Mort
,
Susanna Lualdi
,
et al.
Journal articles
inserm-00604396v1
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[Epilepsy surgery in children: from a multidisciplinary network to the creation of an expertise and care centre]
Alexis Arzimanoglou
,
M. Bourgeois
,
Philippe Kahane
,
Edouard Hirsch
,
N. Boddaert
,
et al.
Journal articles
inserm-00410596v1
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Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.
Sylviane Darquy
,
Grégoire Moutel
,
Anne-Sophie Lapointe
,
Diane d'Audiffret
,
Julie Champagnat
,
et al.
Journal articles
inserm-01179381v1
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Are Developmental Trajectories of Cortical Folding Comparable Between Cross-sectional Datasets of Fetuses and Preterm Newborns?
Julien Lefèvre
,
David Germanaud
,
Jessica Dubois
,
Ines de Macedo Santos
,
Hugo Angleys
,
et al.
Journal articles
hal-01342582v1
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Exploring the successive waves of cortical folding in the developing brain using MRI and spectral analysis of gyrification
Jessica Dubois
,
David Germanaud
,
Hugo Angleys
,
François Leroy
,
Clara Fischer
,
et al.
Conference papers
hal-01458746v1
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Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease
Julien Masliah-Planchon
,
Céline Dupont
,
George Vartzelis
,
Aurélien Trimouille
,
Eléonore Eymard-Pierre
,
et al.
Journal articles
inserm-01264503v1
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MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.
Nathalie Le Meur
,
Muriel Holder-Espinasse
,
Sylvie Jaillard
,
Alice Goldenberg
,
Sylvie Joriot
,
et al.
Journal articles
inserm-00406331v1
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