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

Year Number of Results
2008 2
2010 2
2011 2
2012 2
2013 1
2014 1
2015 1
2016 1
2019 1
2021 1
2022 1
2023 1
2024 0

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15 results

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Page 1
Excessive vomiting.
Renard D, Jeanjean L, Labauge P. Renard D, et al. Among authors: jeanjean l. Eur Neurol. 2012;67(2):90-1. doi: 10.1159/000335071. Epub 2011 Dec 31. Eur Neurol. 2012. PMID: 22212859 No abstract available.
Progressive ataxia related to PRRT2 gene mutation.
Castelnovo G, Renard D, De Verdal M, Luc J, Thouvenot E, Riant F. Castelnovo G, et al. Among authors: luc j. J Neurol Sci. 2016 Aug 15;367:220-1. doi: 10.1016/j.jns.2016.05.058. Epub 2016 May 31. J Neurol Sci. 2016. PMID: 27423591 No abstract available.
Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy.
Charif M, Chevrollier A, Gueguen N, Kane S, Bris C, Goudenège D, Desquiret-Dumas V, Meunier I, Mochel F, Jeanjean L, Varenne F, Procaccio V, Reynier P, Bonneau D, Amati-Bonneau P, Lenaers G. Charif M, et al. Among authors: jeanjean l. Genes (Basel). 2022 Jul 5;13(7):1202. doi: 10.3390/genes13071202. Genes (Basel). 2022. PMID: 35885985 Free PMC article.
Wallenberg syndrome and "neurotrophic" ulcerations.
Taieb G, Renard D, Jeanjean L, Stoebner P. Taieb G, et al. Among authors: jeanjean l. Acta Neurol Belg. 2014 Jun;114(2):143-4. doi: 10.1007/s13760-013-0266-7. Epub 2014 Mar 13. Acta Neurol Belg. 2014. PMID: 24622965 No abstract available.
Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model.
Jurkute N, Bertacchi M, Arno G, Tocco C, Kim US, Kruszewski AM, Avery RA, Bedoukian EC, Han J, Ahn SJ, Pontikos N, Acheson J, Davagnanam I, Bowman R, Kaliakatsos M, Gardham A, Wakeling E, Oluonye N, Reddy MA, Clark E, Rosser E, Amati-Bonneau P, Charif M, Lenaers G, Meunier I, Defoort S, Vincent-Delorme C, Robson AG, Holder GE, Jeanjean L, Martinez-Monseny A, Vidal-Santacana M, Dominici C, Gaggioli C, Giordano N, Caleo M, Liu GT; Genomics England Research Consortium; Webster AR, Studer M, Yu-Wai-Man P. Jurkute N, et al. Among authors: jeanjean l. Brain Commun. 2021 Jul 20;3(3):fcab162. doi: 10.1093/braincomms/fcab162. eCollection 2021. Brain Commun. 2021. PMID: 34466801 Free PMC article.
Optical coherence tomography in neuromyelitis optica.
de Seze J, Blanc F, Jeanjean L, Zéphir H, Labauge P, Bouyon M, Ballonzoli L, Castelnovo G, Fleury M, Defoort S, Vermersch P, Speeg C. de Seze J, et al. Among authors: jeanjean l. Arch Neurol. 2008 Jul;65(7):920-3. doi: 10.1001/archneur.65.7.920. Arch Neurol. 2008. PMID: 18625858
Heterochromia Iridis in congenital Horner's syndrome.
Renard D, Jeanjean L, Labauge P. Renard D, et al. Among authors: jeanjean l. Eur Neurol. 2010;63(4):253. doi: 10.1159/000276946. Epub 2010 Apr 7. Eur Neurol. 2010. PMID: 20375515 Free article. No abstract available.
15 results