1. Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!. Issue 8 (27th July 2019) Authors: Roubertie, Agathe; Charif, Majida; Meyer, Pierre; Manes, Gael; Meunier, Isabelle; Taieb, Guillaume; Junta Morales, Raul; Guichet, Agnès; Delettre, Cecile; Sarzi, Emmanuelle; Leboucq, Nicolas; Rivier, François; Lenaers, Guy Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 8(2019) Page Start: 1572 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Le droit OHADA et le droit international privé : les règles d'applicabilité du droit uniforme. (28th February 2018) Authors: Meyer, Pierre Journal: Uniform law review = Issue: Volume 23:Number 1(2018) Page Start: 99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Prognostic factors for the sequelae and severity of Guillain‐Barré syndrome in children. Issue 6 (23rd October 2019) Authors: Estrade, Sophie; Guiomard, Clara; Fabry, Vincent; Baudou, Eloise; Cances, Claude; Chaix, Yves; Cintas, Pascal; Meyer, Pierre; Cheuret, Emmanuel Journal: Muscle & nerve Issue: Volume 60:Issue 6(2019) Page Start: 716 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Transcatheter valve-in-valve implantation in a degenerated very small Mitroflow prosthesis. (15th June 2018) Authors: Lopez, Stéphane; Meyer, Pierre; Teboul, Jacques; Deharo, Pierre; Mihoubi, Alain; Elbeze, Jean Pierre; Lena, Diane; Camarasa, Philippe; Laborde, Jean Claude; Drogoul, Laurent Journal: Interactive cardiovascular and thoracic surgery Issue: Volume 27:Number 6(2018) Page Start: 850 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical Features and Risk of Relapse in Children and Adults with Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease. Issue 1 (15th October 2020) Authors: Cobo‐Calvo, Alvaro; Ruiz, Anne; Rollot, Fabien; Arrambide, Georgina; Deschamps, Romain; Maillart, Elisabeth; Papeix, Caroline; Audoin, Bertrand; Lépine, Anne Fabienne; Maurey, Hélène; Zephir, Helene; Biotti, Damien; Ciron, Jonathan; Durand‐Dubief, Francoise; Collongues, Nicolas; Ayrignac, Xavier;... Journal: Annals of neurology Issue: Volume 89:Issue 1(2021) Page Start: 30 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Monocentric retrospective clinical outcome in a group of 13 patients with opsoclonus myoclonus syndrome, proposal of diagnostic algorithm and review of the literature. (September 2022) Authors: Urtiaga Valle, Sarai; Souvannanorath, Sarah; Leboucq, Nicolas; Haouy, Stephanie; Rivier, François; Roubertie, Agathe; Meyer, Pierre Journal: European journal of paediatric neurology Issue: Volume 40(2022) Page Start: 18 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies. (9th August 2022) Authors: François‐Heude, Marie‐Céline; Lebigot, Elise; Roze, Emmanuel; Warde, Marie Thérèse Abi; Cances, Claude; Damaj, Lena; Espil, Caroline; Fluss, Joel; de Lonlay, Pascale; Kern, Ilse; Lenaers, Guy; Munnich, Arnold; Meyer, Pierre; Spitz, Marie‐Aude; Torre, Stéphanie; Doummar, Diane; Touati, Guy; Lebouc... Journal: European journal of neurology Issue: Volume 29:Number 11(2022) Page Start: 3229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. Issue 1 (4th October 2019) Authors: Bar, Claire; Barcia, Giulia; Jennesson, Mélanie; Le Guyader, Gwenaël; Schneider, Amy; Mignot, Cyril; Lesca, Gaetan; Breuillard, Delphine; Montomoli, Martino; Keren, Boris; Doummar, Diane; Billette de Villemeur, Thierry; Afenjar, Alexandra; Marey, Isabelle; Gerard, Marion; Isnard, Hervé; Poisson, ... Journal: Human mutation Issue: Volume 41:Issue 1(2020) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. FGF14‐related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9. Issue 4 (12th March 2020) Authors: Piarroux, Julie; Riant, Florence; Humbertclaude, Véronique; Remerand, Ganaelle; Hadjadj, Jessica; Rejou, Franck; Coubes, Christine; Pinson, Lucile; Meyer, Pierre; Roubertie, Agathe Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 4(2020) Page Start: 565 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome. (21st September 2020) Authors: Bar, Claire; Kuchenbuch, Mathieu; Barcia, Giulia; Schneider, Amy; Jennesson, Mélanie; Le Guyader, Gwenaël; Lesca, Gaetan; Mignot, Cyril; Montomoli, Martino; Parrini, Elena; Isnard, Hervé; Rolland, Anne; Keren, Boris; Afenjar, Alexandra; Dorison, Nathalie; Sadleir, Lynette G.; Breuillard, Delphine... Journal: Epilepsia Issue: Volume 61:issue 11(2020) Page Start: 2461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗