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

Year Number of Results
1991 1
1994 1
1995 3
1996 2
1998 1
2002 1
2004 1
2005 1
2006 1
2008 3
2009 5
2010 2
2011 3
2012 2
2013 1
2014 4
2015 2
2017 1
2018 1
2019 2
2020 5
2021 6
2022 6
2023 3
2024 2

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53 results

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Page 1
Neurologic manifestations of giant cell arteritis.
Soulages A, Sibon I, Vallat JM, Ellie E, Bourdain F, Duval F, Carla L, Martin-Négrier ML, Solé G, Laurent C, Monnier A, Le Masson G, Mathis S. Soulages A, et al. Among authors: martin negrier ml. J Neurol. 2022 Jul;269(7):3430-3442. doi: 10.1007/s00415-022-10991-6. Epub 2022 Feb 6. J Neurol. 2022. PMID: 35124749 Review.
Peripheral neuropathy and livedoid vasculopathy.
Soulages A, Maisonobe T, Auzou P, Petit A, Allenbach Y, Barète S, Skopinski S, Ribeiro E, Jullié ML, Lamant L, Brevet F, Soulages X, Vallat JM, Martin-Négrier ML, Solé G, Duval F, Carla L, Le Masson G, Mathis S. Soulages A, et al. Among authors: martin negrier ml. J Neurol. 2022 Jul;269(7):3779-3788. doi: 10.1007/s00415-022-11007-z. Epub 2022 Feb 15. J Neurol. 2022. PMID: 35166926 Review.
Fasciitis secondary to systemic necrotizing vasculitis.
Prot-Leurent C, Martin-Negrier ML, Lazaro E, Delbrel X, Viallard JF. Prot-Leurent C, et al. Among authors: martin negrier ml. QJM. 2022 Mar 22;115(3):164-166. doi: 10.1093/qjmed/hcab308. QJM. 2022. PMID: 34878145 No abstract available.
An update on nerve biopsy.
Vallat JM, Vital A, Magy L, Martin-Negrier ML, Vital C. Vallat JM, et al. Among authors: martin negrier ml. J Neuropathol Exp Neurol. 2009 Aug;68(8):833-44. doi: 10.1097/NEN.0b013e3181af2b9c. J Neuropathol Exp Neurol. 2009. PMID: 19606069 Review.
Mutation on MT-CO2 gene induces mitochondrial disease associated with neurodegeneration and intracerebral iron accumulation (NBIA).
Courtois S, Angelini C, M Durand C, Dias Amoedo N, Courreges A, Dumon E, Le Quang M, Goizet C, Martin-Negrier ML, Rossignol R, Lacombe D, Coupry I, Trimouille A. Courtois S, et al. Among authors: martin negrier ml. Biochim Biophys Acta Mol Basis Dis. 2024 Jan;1870(1):166856. doi: 10.1016/j.bbadis.2023.166856. Epub 2023 Aug 26. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 37640115
Adult onset tubulo-interstitial nephropathy in MT-ND5-related phenotypes.
Bakis H, Trimouille A, Vermorel A, Redonnet I, Goizet C, Boulestreau R, Lacombe D, Combe C, Martin-Négrier ML, Rigothier C. Bakis H, et al. Among authors: martin negrier ml. Clin Genet. 2020 Apr;97(4):628-633. doi: 10.1111/cge.13670. Epub 2020 Jan 9. Clin Genet. 2020. PMID: 31713837
Normal meninges harbor oncogenic somatic mutations in meningioma-driver genes.
Boetto J, Plu I, Ducos Y, Blouin A, Teranishi Y; Brainbank Neuro-CEB Neuropathology Network; Bizzotto S, Kalamarides M, Peyre M. Boetto J, et al. Acta Neuropathol. 2023 Dec;146(6):833-835. doi: 10.1007/s00401-023-02635-4. Epub 2023 Sep 26. Acta Neuropathol. 2023. PMID: 37750907 No abstract available.
Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON).
Vital C, Julien J, Martin-Negrier ML, Lagueny A, Ferrer X, Vital A. Vital C, et al. Among authors: martin negrier ml. Rev Neurol (Paris). 2015 Sep;171(8-9):679-80. doi: 10.1016/j.neurol.2015.03.011. Epub 2015 Apr 24. Rev Neurol (Paris). 2015. PMID: 25917160 Review. No abstract available.
Increased prevalence of granulovacuolar degeneration in C9orf72 mutation.
Riku Y, Duyckaerts C, Boluda S, Plu I, Le Ber I, Millecamps S, Salachas F; Brainbank NeuroCEB Neuropathology Network; Yoshida M, Ando T, Katsuno M, Sobue G, Seilhean D. Riku Y, et al. Acta Neuropathol. 2019 Nov;138(5):783-793. doi: 10.1007/s00401-019-02028-6. Epub 2019 May 29. Acta Neuropathol. 2019. PMID: 31144027
53 results