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Page 1
Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy.
Scheidecker S, Bär S, Stoetzel C, Geoffroy V, Lannes B, Rinaldi B, Fischer F, Becker HD, Pelletier V, Pagan C, Acquaviva-Bourdain C, Kremer S, Mirande M, Tranchant C, Muller J, Friant S, Dollfus H. Scheidecker S, et al. Among authors: lannes b. Hum Mutat. 2019 Oct;40(10):1826-1840. doi: 10.1002/humu.23799. Epub 2019 Jun 18. Hum Mutat. 2019. PMID: 31116475 Free article.
[Mannosidosis type II].
Tranchant C, Reis J, Dietemann JL, Lannes B, Maire I, Warter JM. Tranchant C, et al. Among authors: lannes b. Rev Neurol (Paris). 1991;147(5):364-7. Rev Neurol (Paris). 1991. PMID: 1853034 Review. French.
Myopathies in the elderly: a hospital-based study.
Echaniz-Laguna A, Mohr M, Lannes B, Tranchant C. Echaniz-Laguna A, et al. Among authors: lannes b. Neuromuscul Disord. 2010 Jul;20(7):443-7. doi: 10.1016/j.nmd.2010.05.003. Epub 2010 Jun 1. Neuromuscul Disord. 2010. PMID: 20621722
Magnetic Resonance Imaging of Cerebral Aspergillosis: Imaging and Pathological Correlations.
Marzolf G, Sabou M, Lannes B, Cotton F, Meyronet D, Galanaud D, Cottier JP, Grand S, Desal H, Kreutz J, Schenck M, Meyer N, Schneider F, Dietemann JL, Koob M, Herbrecht R, Kremer S. Marzolf G, et al. Among authors: lannes b. PLoS One. 2016 Apr 20;11(4):e0152475. doi: 10.1371/journal.pone.0152475. eCollection 2016. PLoS One. 2016. PMID: 27097323 Free PMC article.
Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.
Gebus O, Montaut S, Monga B, Wirth T, Cheraud C, Alves Do Rego C, Zinchenko I, Carré G, Hamdaoui M, Hautecloque G, Nguyen-Them L, Lannes B, Chanson JB, Lagha-Boukbiza O, Fleury MC, Devys D, Nicolas G, Rudolf G, Bereau M, Mallaret M, Renaud M, Acquaviva C, Koenig M, Koob M, Kremer S, Namer IJ, Cazeneuve C, Echaniz-Laguna A, Tranchant C, Anheim M. Gebus O, et al. Among authors: lannes b. J Neurol. 2017 Jun;264(6):1118-1126. doi: 10.1007/s00415-017-8500-5. Epub 2017 May 6. J Neurol. 2017. PMID: 28478596
Deep brain stimulation does not enhance neuroinflammation in multiple system atrophy.
Lopez-Cuina M, Fernagut PO, Canron MH, Vital A, Lannes B, De Paula AM, Streichenberger N, Guehl D, Damier P, Eusebio A, Houeto JL, Tison F, Tranchant C, Viallet F, Witjas T, Thobois S, Meissner WG. Lopez-Cuina M, et al. Among authors: lannes b. Neurobiol Dis. 2018 Oct;118:155-160. doi: 10.1016/j.nbd.2018.07.016. Epub 2018 Jul 17. Neurobiol Dis. 2018. PMID: 30026036
Clinical, histological, and genetic characterization of PYROXD1-related myopathy.
Lornage X, Schartner V, Balbueno I, Biancalana V, Willis T, Echaniz-Laguna A, Scheidecker S, Quinlivan R, Fardeau M, Malfatti E, Lannes B, Sewry C, Romero NB, Laporte J, Böhm J. Lornage X, et al. Among authors: lannes b. Acta Neuropathol Commun. 2019 Aug 27;7(1):138. doi: 10.1186/s40478-019-0781-8. Acta Neuropathol Commun. 2019. PMID: 31455395 Free PMC article.
Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases.
Zereg E, Chaussenot A, Morel G, Bannwarth S, Sacconi S, Soriani MH, Attarian S, Cano A, Pouget J, Bellance R, Tranchant C, Lannes B, de Paula AM, Saadi Ait-El-Mkadem S, Chafino B, Berthet M, Fragaki K, Paquis-Flucklinger V, Rouzier C. Zereg E, et al. Among authors: lannes b. Hum Mutat. 2020 Aug;41(8):1394-1406. doi: 10.1002/humu.24037. Epub 2020 Jun 12. Hum Mutat. 2020. PMID: 32419253
82 results