Search - Inserm - Institut national de la santé et de la recherche médicale Access content directly

Filter your results

18 Results
Structure: Internal structure identifier : 160406
Image document

Oxytocin receptor agonist reduces perinatal brain damage by targeting microglia

Jérôme Mairesse , Manuela Zinni , Julien Pansiot , Rahma Hassan-Abdi , Charlie Demené , et al.
Glia, 2019, 67 (2), pp.345-359. ⟨10.1002/glia.23546⟩
Journal articles inserm-04075780v1
Image document

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 of Hepatology, 2016, 65 (2), pp.377-85. ⟨10.1016/j.jhep.2016.04.017⟩
Journal articles inserm-01321215v1

[Vaccine encephalopathy: a myth collapses?]

Philippe Kahane , Alexis Arzimanoglou
La Presse Médicale, 2007, 36 (10 Pt 1), pp.1339-40. ⟨10.1016/j.lpm.2007.05.025⟩
Journal articles inserm-00410857v1

Nocturnal hypermotor seizures, suggesting frontal lobe epilepsy, can originate in the insula.

Philippe Ryvlin , Lorella Minotti , Geneviève Demarquay , Edouard Hirsch , Alexis Arzimanoglou , et al.
Epilepsia, 2006, 47 (4), pp.755-65. ⟨10.1111/j.1528-1167.2006.00510.x⟩
Journal articles inserm-00388334v1
Image document

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.
European Journal of Paediatric Neurology, 2014, 18 (5), pp.597-603. ⟨10.1016/j.ejpn.2014.04.002⟩
Journal articles inserm-00995366v1
Image document

Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation

Imen Dorboz , Hélène Dumay-Odelot , Karima Boussaid , Yosra Bouyacoub , Pauline Barreau , et al.
Neurology Genetics, 2018, 4 (6), pp.e289. ⟨10.1212/nxg.0000000000000289⟩
Journal articles pasteur-02000258v1
Image document

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 of Neuroinflammation, 2016, 13 (1), pp.307. ⟨10.1186/s12974-016-0773-6⟩
Journal articles inserm-01415098v1
Image document

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

[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.
Neurochirurgie, 2008, 54 (3), pp.484-98. ⟨10.1016/j.neuchi.2008.03.003⟩
Journal articles inserm-00410612v1

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
Journal articles inserm-00388238v1
Image document

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.
PLoS ONE, 2019, 14 (11), pp.e0224132. ⟨10.1371/journal.pone.0224132⟩
Journal articles inserm-02409310v1
Image document

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.
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.40. ⟨10.1186/1750-1172-6-40⟩
Journal articles inserm-00604396v1

[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.
Neurochirurgie, 2008, 54 (3), pp.479-83. ⟨10.1016/j.neuchi.2008.02.017⟩
Journal articles inserm-00410596v1
Image document

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.
European Journal of Human Genetics, 2016, 24 (3), pp.338-43. ⟨10.1038/ejhg.2015.115⟩
Journal articles inserm-01179381v1

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.
Cerebral Cortex, 2016, 26 (7), pp.3023 - 3035. ⟨10.1093/cercor/bhv123⟩
Journal articles hal-01342582v1
Image document

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.
13th IEEE International Symposium on Biomedical Imaging (ISBI 2016), Apr 2016, Prague, Czech Republic. ⟨10.1109/ISBI.2016.7493259⟩
Conference papers hal-01458746v1
Image document

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.
BMC Medical Genetics, 2015, 16 (1), pp.77. ⟨10.1186/s12881-015-0226-6⟩
Journal articles inserm-01264503v1
Image document

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 of Medical Genetics, 2010, 47 (1), pp.22-9. ⟨10.1136/jmg.2009.069732⟩
Journal articles inserm-00406331v1