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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2000 1
2001 1
2002 4
2003 3
2005 3
2006 6
2007 2
2008 1
2009 1
2010 2
2011 1
2012 2
2013 2
2014 1
2015 1
2016 4
2017 3
2018 8
2019 2
2020 1
2021 1
2022 1
2023 1
2024 0

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50 results

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Page 1
Wolfram syndrome: MAMs' connection?
Delprat B, Maurice T, Delettre C. Delprat B, et al. Among authors: delettre c. Cell Death Dis. 2018 Mar 6;9(3):364. doi: 10.1038/s41419-018-0406-3. Cell Death Dis. 2018. PMID: 29511163 Free PMC article. Review.
Dominant optic atrophy.
Lenaers G, Hamel C, Delettre C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P, Milea D. Lenaers G, et al. Among authors: delettre c. Orphanet J Rare Dis. 2012 Jul 9;7:46. doi: 10.1186/1750-1172-7-46. Orphanet J Rare Dis. 2012. PMID: 22776096 Free PMC article. Review.
Mitochondrial dynamics and disease, OPA1.
Olichon A, Guillou E, Delettre C, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Daloyau M, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Belenguer P. Olichon A, et al. Among authors: delettre c. Biochim Biophys Acta. 2006 May-Jun;1763(5-6):500-9. doi: 10.1016/j.bbamcr.2006.04.003. Epub 2006 Apr 20. Biochim Biophys Acta. 2006. PMID: 16737747 Free article. Review.
OPA1 functions in mitochondria and dysfunctions in optic nerve.
Lenaers G, Reynier P, Elachouri G, Soukkarieh C, Olichon A, Belenguer P, Baricault L, Ducommun B, Hamel C, Delettre C. Lenaers G, et al. Among authors: delettre c. Int J Biochem Cell Biol. 2009 Oct;41(10):1866-74. doi: 10.1016/j.biocel.2009.04.013. Epub 2009 Apr 21. Int J Biochem Cell Biol. 2009. PMID: 19389483 Free article. Review.
Reply: The expanding neurological phenotype of DNM1L-related disorders.
Gerber S, Charif M, Chevrollier A, Chaumette T, Angebault C, Kane S, Paris A, Alban J, Quiles M, Delettre C, Bonneau D, Procaccio V, Amati-Bonneau P, Reynier P, Leruez S, Calmon R, Boddaert N, Funalot B, Rio M, Bouccara D, Meunier I, Sesaki H, Kaplan J, Hamel CP, Rozet JM, Lenaers G. Gerber S, et al. Among authors: delettre c. Brain. 2018 Apr 1;141(4):e29. doi: 10.1093/brain/awy027. Brain. 2018. PMID: 29529130 No abstract available.
Mitochondrial Complex I activity signals antioxidant response through ERK5.
Khan AUH, Allende-Vega N, Gitenay D, Garaude J, Vo DN, Belkhala S, Gerbal-Chaloin S, Gondeau C, Daujat-Chavanieu M, Delettre C, Orecchioni S, Talarico G, Bertolini F, Anel A, Cuezva JM, Enriquez JA, Cartron G, Lecellier CH, Hernandez J, Villalba M. Khan AUH, et al. Among authors: delettre c. Sci Rep. 2018 May 9;8(1):7420. doi: 10.1038/s41598-018-23884-4. Sci Rep. 2018. PMID: 29743487 Free PMC article.
Structural basis of envelope and phase intrinsic coupling modes in the cerebral cortex.
Messé A, Hollensteiner KJ, Delettre C, Dell-Brown LA, Pieper F, Nentwig LJ, Galindo-Leon EE, Larrat B, Mériaux S, Mangin JF, Reillo I, de Juan Romero C, Borrell V, Engler G, Toro R, Engel AK, Hilgetag CC. Messé A, et al. Among authors: delettre c. Neuroimage. 2023 Aug 1;276:120212. doi: 10.1016/j.neuroimage.2023.120212. Epub 2023 Jun 1. Neuroimage. 2023. PMID: 37269959 Free PMC article.
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy.
Piro-Mégy C, Sarzi E, Tarrés-Solé A, Péquignot M, Hensen F, Quilès M, Manes G, Chakraborty A, Sénéchal A, Bocquet B, Cazevieille C, Roubertie A, Müller A, Charif M, Goudenège D, Lenaers G, Wilhelm H, Kellner U, Weisschuh N, Wissinger B, Zanlonghi X, Hamel C, Spelbrink JN, Sola M, Delettre C. Piro-Mégy C, et al. Among authors: delettre c. J Clin Invest. 2020 Jan 2;130(1):143-156. doi: 10.1172/JCI128513. J Clin Invest. 2020. PMID: 31550237 Free PMC article.
50 results