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Authors: Gaëlle Augé
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Journal Article
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease models
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Baptiste Ropert and others
Brain, awae348, https://doi.org/10.1093/brain/awae348
Published: 30 October 2024
Journal Article
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability
Emmanuelle C Genin and others
Brain, Volume 145, Issue 10, October 2022, Pages 3415–3430, https://doi.org/10.1093/brain/awac197
Published: 03 June 2022
Journal Article
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China
Sylvie Bannwarth and others
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?
Sylvie Bannwarth and others
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
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Sylvie Bannwarth and others
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
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Sylvie Bannwarth and others
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?
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Sylvie Bannwarth and others
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
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Sylvie Bannwarth and others
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
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Sylvie Bannwarth and others
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
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Sylvie Bannwarth and others
Brain, Volume 137, Issue 8, August 2014, Pages 2329–2345, https://doi.org/10.1093/brain/awu138
Published: 13 June 2014
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