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Authors: Annabelle Chaussenot
Journal Article
De novo and inherited monoallelic variants in TUBA4A cause ataxia and spasticity Get access
Brain, Volume 147, Issue 11, November 2024, Pages 3681–3689, https://doi.org/10.1093/brain/awae193
Published: 17 June 2024
Journal Article
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China
Brain, Volume 139, Issue 4, April 2016, Page e22, https://doi.org/10.1093/brain/awv368
Published: 30 December 2015
Journal Article
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Brain, Volume 138, Issue 10, October 2015, Page e386, https://doi.org/10.1093/brain/awv116
Published: 07 May 2015
Journal Article
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation Get access
Brain, Volume 138, Issue 9, September 2015, Page e377, https://doi.org/10.1093/brain/awv015
Published: 13 February 2015
Journal Article
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis Get access
Brain, Volume 138, Issue 8, August 2015, Page e373, https://doi.org/10.1093/brain/awu385
Published: 09 January 2015
Journal Article
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis? Get access
Brain, Volume 137, Issue 12, December 2014, Page e314, https://doi.org/10.1093/brain/awu300
Published: 10 October 2014
Journal Article
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis Get access
Brain, Volume 137, Issue 12, December 2014, Page e312, https://doi.org/10.1093/brain/awu267
Published: 26 September 2014
Journal Article
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease Get access
Brain, Volume 137, Issue 12, December 2014, Page e310, https://doi.org/10.1093/brain/awu228
Published: 09 August 2014
Journal Article
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement Get access
Brain, Volume 137, Issue 8, August 2014, Pages 2329–2345, https://doi.org/10.1093/brain/awu138
Published: 13 June 2014
Journal Article
Reply: MFN2, a new gene responsible for mitochondrial DNA depletion Get access
Brain, Volume 135, Issue 8, August 2012, Page e224, https://doi.org/10.1093/brain/aws112
Published: 16 May 2012
Journal Article
Reply: MFN2 mutations cause compensatory mitochondrial DNA proliferation Get access
Brain, Volume 135, Issue 8, August 2012, Page e220, https://doi.org/10.1093/brain/aws052
Published: 04 April 2012
Journal Article
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy ‘plus’ phenotype Get access
Brain, Volume 135, Issue 1, January 2012, Pages 23–34, https://doi.org/10.1093/brain/awr323
Published: 20 December 2011
