Charlotte Cochaud

Nice, France

Last Updated: 09/26/2026

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Found 13 publications

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability.

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability.

Journal: Brain : a journal of neurology
Published: July 27, 2021

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse.

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse.

Journal: Acta neuropathologica
Published: December 14, 2018

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases.

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases.

Journal: Neurobiology of disease
Published: February 16, 2018

Severe defect in mitochondrial complex I assembly with mitochondrial DNA deletions in ACAD9-deficient mild myopathy.

Severe defect in mitochondrial complex I assembly with mitochondrial DNA deletions in ACAD9-deficient mild myopathy.

Journal: Muscle & nerve
Published: July 18, 2016

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

Journal: Brain : a journal of neurology
Published: January 01, 2016

Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes.

Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes.

Journal: Biological research
Published: September 24, 2015

Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

Journal: Brain : a journal of neurology
Published: May 09, 2015

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

Journal: Brain : a journal of neurology
Published: February 15, 2015

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology
Published: January 11, 2015

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Journal: Brain : a journal of neurology
Published: October 29, 2014

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology
Published: September 29, 2014

Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

Journal: Brain : a journal of neurology
Published: August 13, 2014
Showing 1-12 of 13

Last Updated: 09/26/2026