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Thermal Stability of Al-Cu-Mg Alloys

Materials science forum, 2014-06, Vol.794-796, p.691-696

2014

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Compréhension de la stabilité thermique des alliages d'aluminium Al-Cu-Mg Understanding of the thermal stability of Al-Cu-Mg aluminum alloys

MATEC web of conferences, 2013-11, Vol.7, p.01015

2013

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Compréhension de la stabilité thermique des alliages d'aluminium Al-Cu-Mg

MATEC web of conferences, 2013, Vol.7, p.1015

2013

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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Brain (London, England : 1878), 2014-08, Vol.137 (Pt 8), p.2329-2345

2014

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Dolutegravir Monotherapy Versus Dolutegravir/Abacavir/Lamivudine for Virologically Suppressed People Living With Chronic Human Immunodeficiency Virus Infection: The Randomized Noninferiority MONotherapy of TiviCAY Trial

Clinical infectious diseases, 2019-10, Vol.69 (9), p.1498-1505

2019

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Thermodynamic and Structural Investigation of Synthetic Actinide–Peptide Scaffolds

Inorganic chemistry, 2016-01, Vol.55 (2), p.877-886

2016

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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Neurobiology of aging, 2014-12, Vol.35 (12), p.2884.e1-2884.e4

2014

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Human diaphragm atrophy in amyotrophic lateral sclerosis is not predicted by routine respiratory measures

The European respiratory journal, 2019-02, Vol.53 (2), p.1801749

2019

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CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy

Annals of neurology, 2015-11, Vol.78 (5), p.831-831

2015

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A modular architecture for organizing, processing and sharing neurophysiology data

Nature methods, 2023-03, Vol.20 (3), p.403-407

2023

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

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.e386-e386

2015

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Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China: Table 1

Brain (London, England : 1878), 2016-04, Vol.139 (4), p.e22-e22

2016

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Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation: Table 1

Brain (London, England : 1878), 2015-09, Vol.138 (9), p.e377-e377

2015

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Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322–324

Journal of the neurological sciences, 2015-04, Vol.351 (1), p.196-197

2015

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

Brain (London, England : 1878), 2015-09, Vol.138 (Pt 9), p.e377-e377

2015

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

Brain (London, England : 1878), 2016-04, Vol.139 (Pt 4), p.e22-e22

2016

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Lightning Pose: improved animal pose estimation via semi-supervised learning, Bayesian ensembling and cloud-native open-source tools

Nature methods, 2024-07, Vol.21 (7), p.1316-1328

2024

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

Brain (London, England : 1878), 2014-12, Vol.137 (Pt 12), p.e310-e310

2014

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

Brain (London, England : 1878), 2015-08, Vol.138 (Pt 8), p.e373-e373

2015

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

Brain (London, England : 1878), 2014-12, Vol.137 (Pt 12), p.e312-e312

2014

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

Brain (London, England : 1878), 2014-12, Vol.137 (Pt 12), p.e314-e314

2014

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Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis

Archives of neurology (Chicago), 2008-10, Vol.65 (10), p.1333

2008

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Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: A French national survey

Amyotrophic lateral sclerosis, 2011-05, Vol.12 (3), p.178-184

2011

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Clinical Neurology
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Mitochondrial Proteins - Genetics
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Amyotrophic Lateral Sclerosis - Etiology
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Thermal Stability of Al-Cu-Mg Alloys

Compréhension de la stabilité thermique des alliages d'aluminium Al-Cu-Mg Understanding of the thermal stability of Al-Cu-Mg aluminum alloys

Compréhension de la stabilité thermique des alliages d'aluminium Al-Cu-Mg

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Dolutegravir Monotherapy Versus Dolutegravir/Abacavir/Lamivudine for Virologically Suppressed People Living With Chronic Human Immunodeficiency Virus Infection: The Randomized Noninferiority MONotherapy of TiviCAY Trial

Thermodynamic and Structural Investigation of Synthetic Actinide–Peptide Scaffolds

Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Human diaphragm atrophy in amyotrophic lateral sclerosis is not predicted by routine respiratory measures

CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy

A modular architecture for organizing, processing and sharing neurophysiology data

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

Penser le vivant

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China: Table 1

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation: Table 1

Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322–324

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

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

Lightning Pose: improved animal pose estimation via semi-supervised learning, Bayesian ensembling and cloud-native open-source tools

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

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

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

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

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis

Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: A French national survey

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