1. A Novel RAB33B Mutation in Smith–McCort Dysplasia. Issue 2 (8th November 2012) Authors: Dupuis, Nina; Lebon, Sophie; Kumar, Manoj; Drunat, Séverine; Graul‐Neumann, Luitgard M.; Gressens, Pierre; El Ghouzzi, Vincent Journal: Human mutation Issue: Volume 34:Issue 2(2013:Feb.) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory. (January 2016) Authors: Passemard, Sandrine; Verloes, Alain; Billette de Villemeur, Thierry; Boespflug-Tanguy, Odile; Hernandez, Karen; Laurent, Marion; Isidor, Bertrand; Alberti, Corinne; Pouvreau, Nathalie; Drunat, Séverine; Gérard, Bénédicte; El Ghouzzi, Vincent; Gallego, Jorge; Elmaleh-Bergès, Monique; Huttner, Wiel... Journal: Cortex Issue: Volume 74(2016) Page Start: 158 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory. (January 2016) Authors: Passemard, Sandrine; Verloes, Alain; Billette de Villemeur, Thierry; Boespflug-Tanguy, Odile; Hernandez, Karen; Laurent, Marion; Isidor, Bertrand; Alberti, Corinne; Pouvreau, Nathalie; Drunat, Séverine; Gérard, Bénédicte; El Ghouzzi, Vincent; Gallego, Jorge; Elmaleh-Bergès, Monique; Huttner, Wiel... Journal: Cortex Issue: Volume 74(2016) Page Start: 158 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal recessive primary microcephaly due to ASPM mutations: An update. Issue 3 (16th January 2018) Authors: Létard, Pascaline; Drunat, Séverine; Vial, Yoann; Duerinckx, Sarah; Ernault, Anais; Amram, Daniel; Arpin, Stéphanie; Bertoli, Marta; Busa, Tiffany; Ceulemans, Berten; Desir, Julie; Doco‐Fenzy, Martine; Elalaoui, Siham Chafai; Devriendt, Koenraad; Faivre, Laurence; Francannet, Christine; Geneviève... Journal: Human mutation Issue: Volume 39:Issue 3(2018) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects. Issue 6 (3rd February 2020) Authors: Nasser, Hala; Vera, Liza; Elmaleh-Bergès, Monique; Steindl, Katharina; Letard, Pascaline; Teissier, Natacha; Ernault, Anais; Guimiot, Fabien; Afenjar, Alexandra; Moutard, Marie Laure; Héron, Delphine; Alembik, Yves; Momtchilova, Martha; Milani, Paolo; Kubis, Nathalie; Pouvreau, Nathalie; Zollino,... Journal: Journal of medical genetics Issue: Volume 57:Issue 6(2020) Page Start: 389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Conditional Induction of Math1 Specifies Embryonic Stem Cells to Cerebellar Granule Neuron Lineage and Promotes Differentiation into Mature Granule Neurons123. (20th March 2013) Authors: Srivastava, Rupali; Kumar, Manoj; Peineau, Stéphane; Csaba, Zsolt; Mani, Shyamala; Gressens, Pierre; El Ghouzzi, Vincent Journal: Stem cells Issue: Volume 31:Number 4(2013:Apr.) Page Start: 652 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Correction to: ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly. Issue 12 (December 2018) Authors: El Ghouzzi, Vincent; Bianchi, Federico; Molineris, Ivan; Mounce, Bryan; Berto, Gaia; Rak, Malgorzata; Lebon, Sophie; Aubry, Laetitia; Tocco, Chiara; Gai, Marta; Chiotto, Alessandra; Sgrò, Francesco; Pallavicini, Gianmarco; Simon-Loriere, Etienne; Passemard, Sandrine; Vignuzzi, Marco; Gressens, Pi... Journal: Cell death and disease Issue: Volume 9:Issue 12(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Endogenous cerebellar neurogenesis in adult mice with progressive ataxia. (4th November 2014) Authors: Kumar, Manoj; Csaba, Zsolt; Peineau, Stéphane; Srivastava, Rupali; Rasika, Sowmyalakshmi; Mani, Shyamala; Gressens, Pierre; El Ghouzzi, Vincent Journal: Annals of clinical and translational neurology Issue: Volume 1:Number 12(2014) Page Start: 968 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Golgi trafficking defects in postnatal microcephaly: The evidence for "Golgipathies". (June 2017) Authors: Passemard, Sandrine; Perez, Franck; Colin-Lemesre, Emilie; Rasika, Sowmyalakshmi; Gressens, Pierre; El Ghouzzi, Vincent Journal: Progress in neurobiology Issue: Volume 153(2017:Jun.) Page Start: 46 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. HIP/PAP prevents excitotoxic neuronal death and promotes plasticity. (9th October 2014) Authors: Haldipur, Parthiv; Dupuis, Nina; Degos, Vincent; Moniaux, Nicolas; Chhor, Vibol; Rasika, Sowmyalakshmi; Schwendimann, Leslie; le Charpentier, Tifenn; Rougier, Elodie; Amouyal, Paul; Amouyal, Gilles; Dournaud, Pascal; Bréchot, Christian; El Ghouzzi, Vincent; Faivre, Jamila; Fleiss, Bobbi; Mani, Sh... Journal: Annals of clinical and translational neurology Issue: Volume 1:Number 10(2014) Page Start: 739 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗