244
Views
12
CrossRef citations to date
0
Altmetric
Research Article

Minor cognitive disturbances in X-linked spinal and bulbar muscular atrophy, Kennedy's disease

, , , , , , & show all
Pages 15-20 | Received 06 Apr 2013, Accepted 20 Aug 2013, Published online: 08 Nov 2013

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

Emanuele Pick, Johann R Kleinbub, Stefania Mannarini & Arianna Palmieri. (2019) Empathy In Neurodegenerative Diseases: A Systematic Review. Neuropsychiatric Disease and Treatment 15, pages 3287-3304.
Read now

Articles from other publishers (11)

Ben-Chi Cai, Li-Fan Zhong, Yan-Hui Liu, Zhi-Yan Sui, Qiang Yang, Dan-Ting Zeng, Xi Li, Wen-Di Xu & Tao Chen. (2023) Genotype and clinical phenotype analysis of a Family with Kennedy disease. Medicine 102:15, pages e33502.
Crossref
Richard Huan Xu, Ming Lu, Shuyang Zhang & Dong Dong. (2022) EQ-5D and SF-6D health utility scores in patients with spinal and bulbar muscular atrophy. The European Journal of Health Economics.
Crossref
Mary Clare McKenna, Philippe Corcia, Philippe Couratier, We Fong Siah, Pierre-Francois Pradat & Peter Bede. (2021) Frontotemporal Pathology in Motor Neuron Disease Phenotypes: Insights From Neuroimaging. Frontiers in Neurology 12.
Crossref
Arianna Palmieri, Federica Meconi, Antonino Vallesi, Mariagrazia Capizzi, Emanuele Pick, Sonia Marcato, Johann R. Kleinbub, Gianni Sorarù & Paola Sessa. (2020) Enhanced Neural Empathic Responses in Patients with Spino-Bulbar Muscular Atrophy: An Electrophysiological Study. Brain Sciences 11:1, pages 16.
Crossref
Pierre-François Pradat, Emilien Bernard, Philippe Corcia, Philippe Couratier, Christel Jublanc, Giorgia Querin, Capucine Morélot Panzini, François Salachas, Christophe Vial, Karim Wahbi, Peter Bede & Claude Desnuelle. (2020) The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations. Orphanet Journal of Rare Diseases 15:1.
Crossref
Frederick J. Arnold & Diane E. Merry. (2019) Molecular Mechanisms and Therapeutics for SBMA/Kennedy’s Disease. Neurotherapeutics 16:4, pages 928-947.
Crossref
L. Greensmith, P.F. Pradat, G. Sorarù & M. Pennuto. (2019) 241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands. Neuromuscular Disorders 29:9, pages 716-724.
Crossref
Edoardo G. Spinelli, Federica Agosta, Pilar M. Ferraro, Giorgia Querin, Nilo Riva, Cinzia Bertolin, Ilaria Martinelli, Christian Lunetta, Andrea Fontana, Gianni Sorarù & Massimo Filippi. (2019) Brain MRI shows white matter sparing in Kennedy's disease and slow‐progressing lower motor neuron disease. Human Brain Mapping.
Crossref
Giorgia Querin, Peter Bede, Veronique Marchand-Pauvert & Pierre-Francois Pradat. (2018) Biomarkers of Spinal and Bulbar Muscle Atrophy (SBMA): A Comprehensive Review. Frontiers in Neurology 9.
Crossref
S. Marcato, J. R. Kleinbub, G. Querin, E. Pick, I. Martinelli, C. Bertolin, S. Cipolletta, E. Pegoraro, G. Sorarù & A. Palmieri. (2018) Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study. Scientific Reports 8:1.
Crossref
Jeffrey Rosenfeld & Michael J. Strong. (2015) Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease. Neurotherapeutics 12:2, pages 317-325.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.