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authFullName_s : Sandra Lacas-Gervais

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2014, 137 (12), pp.e310. ⟨10.1093/brain/awu228⟩
Journal articles hal-01060685v1
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EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesis

Mariagrazia Partisani , Carole L Baron , Rania Ghossoub , Racha Fayad , Sophie Pagnotta et al.
Journal of Cell Science, 2021, 134 (2), pp.jcs249565. ⟨10.1242/jcs.249565⟩
Journal articles hal-03120586v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2014, 137 (Pt 8), pp.2329-45. ⟨10.1093/brain/awu138⟩
Journal articles hal-01059178v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C. Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2016, 139 (4), pp.e22. ⟨10.1093/brain/awv368⟩
Journal articles hal-01336629v1

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

Emmanuelle C Genin , Sylvie Bannwarth , Baptiste Ropert , Françoise Lespinasse , Alessandra Mauri-Crouzet et al.
Brain - A Journal of Neurology , 2022, 145 (10), pp.3415-3430. ⟨10.1093/brain/awac197⟩
Journal articles pasteur-03853884v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle Génin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2014, 137 (12), pp.e312-e312. ⟨10.1093/brain/awu267⟩
Journal articles hal-02108988v1
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Identification of adipocytes as target cells for Leishmania infantum parasites

Aurélie Schwing , Didier Pisani , Christelle Pomares , Alissa Majoor , Sandra Lacas-Gervais et al.
Scientific Reports, 2021, 11 (1), pp.21275. ⟨10.1038/s41598-021-00443-y⟩
Journal articles pasteur-03744940v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle Génin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2015, 138 (8), pp.e373-e373. ⟨10.1093/brain/awu385⟩
Journal articles hal-02108961v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2015, 138 (Pt 9), pp.e377
Journal articles hal-01218555v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2015, 138 (Pt 10), pp.e386. ⟨10.1093/brain/awv116⟩
Journal articles hal-01272635v1

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

Sylvie Bannwarth , Samira Ait-El-Mkadem , Annabelle Chaussenot , Emmanuelle C Genin , Sandra Lacas-Gervais et al.
Brain - A Journal of Neurology , 2014, 137 (Pt 12), pp.e314. ⟨10.1093/brain/awu300⟩
Journal articles hal-01135688v1
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Aminopeptidase A contributes to biochemical, anatomical and cognitive defects in Alzheimer’s disease (AD) mouse model and is increased at early stage in sporadic AD brain

Audrey Valverde , Julie Dunys , Thomas Lorivel , Delphine Debayle , Anne-Sophie Gay et al.
Acta Neuropathologica, 2021, 141 (6), pp.823-839. ⟨10.1007/s00401-021-02308-0⟩
Journal articles hal-03239400v1