A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation-Reference-Cited by-同舟云学术

A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation

Published:2014-11-21 Issue:2 Volume:43 Page:625-630
ISSN:1875-8908
Container-title:Journal of Alzheimer's Disease
language:
Short-container-title:JAD

Author:

Boutoleau-Bretonnière Claire¹²³,Camuzat Agnès⁴⁵⁶,Le Ber Isabelle⁴⁵⁶⁷⁸,Bouya-Ahmed Kawtar⁴⁵⁶,Guerreiro Rita⁹,Deruet Anne-Laure¹²,Evrard Christelle¹²,Bras José⁹,Lamy Estelle¹²,Auffray-Calvier Elisabeth¹⁰,Pallardy Amandine¹¹,Hardy John⁹,Brice Alexis⁴⁵⁶,Derkinderen Pascal¹²¹²,Vercelletto Martine¹²

Affiliation:

1. CHU Nantes, Centre de Mémoire et de Ressource et Recherche (CM2R), Nantes, France

2. Inserm, CIC 04, Nantes, France

3. Laboratoire d'études des mécanismes cognitifs, EA 3082, Université Lyon 2, Bron F-69500, France

4. Inserm, UMR_S1127, CRICM, F-75013, Paris, France

5. UPMC Univ Paris 06, UMR_S975, F-75013, Paris, France

6. CNRS UMR 7225, F-75013, Paris, France

7. AP-HP, Hôpital de la Pitié-Salpêtrière, Centre de Référence des Démences Rares, F-75013, Paris, France

8. AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, F-75013, Paris, France

9. Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK

10. Service de Neuroradiologie, CHU de Nantes, Nantes, France

11. Service de Médecine Nucléaire, CHU de Nantes, Nantes, France

12. Inserm, UMR 913, Nantes, France

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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