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C9ORF72: What It Is, What It Does, and Why It Matters.
Smeyers J, Banchi EG, Latouche M. Smeyers J, et al. Among authors: latouche m. Front Cell Neurosci. 2021 May 5;15:661447. doi: 10.3389/fncel.2021.661447. eCollection 2021. Front Cell Neurosci. 2021. PMID: 34025358 Free PMC article. Review.
New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers.
Viodé A, Fournier C, Camuzat A, Fenaille F; NeuroCEB Brain Bank; Latouche M, Elahi F, Le Ber I, Junot C, Lamari F, Anquetil V, Becher F. Viodé A, et al. Among authors: latouche m. Front Neurosci. 2018 Aug 28;12:589. doi: 10.3389/fnins.2018.00589. eCollection 2018. Front Neurosci. 2018. PMID: 30210275 Free PMC article.
C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in mice.
Lopez-Herdoiza MB, Bauché S, Wilmet B, Le Duigou C, Roussel D, Frah M, Béal J, Devely G, Boluda S, Frick P, Bouteiller D, Dussaud S, Guillabert P, Dalle C, Dumont M, Camuzat A, Saracino D, Barbier M, Bruneteau G, Ravassard P, Neumann M, Nicole S, Le Ber I, Brice A, Latouche M. Lopez-Herdoiza MB, et al. Among authors: latouche m. Front Cell Neurosci. 2023 Apr 17;17:1155929. doi: 10.3389/fncel.2023.1155929. eCollection 2023. Front Cell Neurosci. 2023. PMID: 37138765 Free PMC article.
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia.
Saracino D, Clot F, Camuzat A, Anquetil V, Hannequin D, Guyant-Maréchal L, Didic M, Guillot-Noël L, Rinaldi D, Latouche M, Forlani S, Ghassab Y, Coppola C, Di Iorio G, David I; French research network on FTD/FTD-ALS; Le Guern E, Brice A, Le Ber I. Saracino D, et al. Among authors: latouche m. Neurobiol Aging. 2018 Dec;72:187.e11-187.e14. doi: 10.1016/j.neurobiolaging.2018.06.037. Epub 2018 Jun 30. Neurobiol Aging. 2018. PMID: 30005904 Free article.
MicroRNA signatures in genetic frontotemporal dementia and amyotrophic lateral sclerosis.
Kmetzsch V, Latouche M, Saracino D, Rinaldi D, Camuzat A, Gareau T; French Research Network on FTD/ALS; Le Ber I, Colliot O, Becker E. Kmetzsch V, et al. Among authors: latouche m. Ann Clin Transl Neurol. 2022 Nov;9(11):1778-1791. doi: 10.1002/acn3.51674. Epub 2022 Oct 20. Ann Clin Transl Neurol. 2022. PMID: 36264717 Free PMC article.
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.
Le Ber I, Camuzat A, Guerreiro R, Bouya-Ahmed K, Bras J, Nicolas G, Gabelle A, Didic M, De Septenville A, Millecamps S, Lenglet T, Latouche M, Kabashi E, Campion D, Hannequin D, Hardy J, Brice A; French Clinical and Genetic Research Network on FTD/FTD-ALS. Le Ber I, et al. Among authors: latouche m. JAMA Neurol. 2013 Nov;70(11):1403-10. doi: 10.1001/jamaneurol.2013.3849. JAMA Neurol. 2013. PMID: 24042580 Free PMC article.
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes.
Le Ber I, Van Bortel I, Nicolas G, Bouya-Ahmed K, Camuzat A, Wallon D, De Septenville A, Latouche M, Lattante S, Kabashi E, Jornea L, Hannequin D, Brice A; French research Network on FTLD/FTLD-ALS. Le Ber I, et al. Among authors: latouche m. Neurobiol Aging. 2014 Apr;35(4):934.e5-6. doi: 10.1016/j.neurobiolaging.2013.09.016. Epub 2013 Oct 9. Neurobiol Aging. 2014. PMID: 24119545
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