Brice Laurens

Parkinson expert - Hospital practitioner

Assistant Professor - PhD (MCU) / Université de Bordeaux IMN clinique

/ Team

IMN clinics
IMN

/ Contact

+33 5 57 82 12 53

www.orcid.org/0000-0001-7797-2703

/ Address of work
IMN Clinique - Hôpital Pellegrin - CHU Bordeaux - 4 place Amélie-Raba-Léon - 33000 Bordeaux

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Scientific articles

Trial of Lixisenatide in Early Parkinson’s Disease
Wassilios G. Meissner, Philippe Remy, Caroline Giordana, David Maltête, Pascal Derkinderen, Jean-Luc Houéto, Mathieu Anheim, Isabelle Benatru, Thomas Boraud, Christine Brefel-Courbon, Nicolas Carrière, Hélène Catala, Olivier Colin, Jean-Christophe Corvol, Philippe Damier, Estelle Dellapina, David Devos, Sophie Drapier, Margherita Fabbri, Vanessa Ferrier, Alexandra Foubert-Samier, Solène Frismand-Kryloff, Aurore Georget, Christine Germain, Stéphane Grimaldi, Clémence Hardy, Lucie Hopes, Pierre Krystkowiak, Brice Laurens, Romain Lefaucheur, Louise-Laure Mariani, Ana Marques, Claire Marse, Fabienne Ory-Magne, Vincent Rigalleau, Hayet Salhi, Amandine Saubion, Simon R. W. Stott, Claire Thalamas, Claire Thiriez, Mélissa Tir, Richard K. Wyse, Antoine Benard, Olivier Rascol.
N Engl J Med. 2024-04-04. 390(13) : 1176-1185.
10.1056/NEJMoa2312323
Care of Late-Stage Parkinsonism: Resource Utilization of the Disease in Five European Countries
Christopher Kruse, Anna Lipinski, Malte Verheyen, Monika Balzer‐Geldsetzer, Michael Wittenberg, Stefan Lorenzl, Carmen Richinger, Christian Schmotz, Lars Tönges, Dirk Woitalla, Stephan Klebe, Bastiaan R. Bloem, Adrianus Hommel, Wassilios G. Meissner, Brice Laurens, Thomas Boraud, Alexandra Foubert‐Samier, Sylvain Vergnet, François Tison, Nadège Costa, Per Odin, Kristina Rosqvist, Jenny M. Norlin, Frida Hjalte, Anette Schrag, Richard Dodel.
Movement Disorders. 2024-02-29. 39(3) : 571-584.
10.1002/mds.29718
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families
Mehdi Benkirane, Cecilia Marelli, Claire Guissart, Agathe Roubertie, Elizabeth Ollagnon, Ariane Choumert, Frédérique Fluchère, Fabienne Ory Magne, Yosra Halleb, Mathilde Renaud, Lise Larrieu, David Baux, Olivier Patat, Idriss Bousquet, Jean-Marie Ravel, Danielle Cuntz-Shadfar, Catherine Sarret, Xavier Ayrignac, Anne Rolland, Raoul Morales, Morgane Pointaux, Cathy Lieutard-Haag, Brice Laurens, Caroline Tillikete, Emilien Bernard, Martial Mallaret, Clarisse Carra-Dallière, Christine Tranchant, Pierre Meyer, Lena Damaj, Laurent Pasquier, Cecile Acquaviva, Annabelle Chaussenot, Bertrand Isidor, Karine Nguyen, William Camu, Alexandre Eusebio, Nicolas Carrière, Audrey Riquet, Eric Thouvenot, Victoria Gonzales, Emilie Carme, Shahram Attarian, Sylvie Odent, Anna Castrioto, Claire Ewenczyk, Perrine Charles, Laurent Kremer, Samira Sissaoui, Nadia Bahi-buisson, Elsa Kaphan, Adrian Degardin, Bérénice Doray, Sophie Julia, Ganaëlle Remerand, Valerie Fraix, Lydia Abou Haidar, Leila Lazaro, Vincent Laugel, Frederic Villega, Cyril Charlin, Solène Frismand, Marinha Costa Moreira, Tatiana Witjas, Christine Francannet, Ulrike Walther-Louvier, Mélanie Fradin, Brigitte Chabrol, Joel Fluss, Eric Bieth, Giovanni Castelnovo, Sylvain Vergnet, Isabelle Meunier, Alain Verloes, Elise Brischoux-Boucher, Christine Coubes, David Geneviève, Nicolas Lebouc, Jean Phillipe Azulay, Mathieu Anheim, Cyril Goizet, François Rivier, Pierre Labauge, Patrick Calvas, Michel Koenig.
Genetics in Medicine. 2021-11-01. 23(11) : 2160-2170.
10.1038/S41436-021-01250-6