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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
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.
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.
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.
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.
Neurologic and vascular abnormalities in Klippel-Trenaunay-Weber syndrome.
Renard D, Campello C, Taieb G, Orgeval J, Jeanjean L, Collombier L, Metge L, Briere C, Castelnovo G, Bonafe A. Renard D, et al. Among authors: jeanjean l. JAMA Neurol. 2013 Jan;70(1):127-8. doi: 10.1001/jamaneurol.2013.587. JAMA Neurol. 2013. PMID: 23090443 No abstract available.
Recurrent cerebral infarction in Klippel-Trenaunay-Weber syndrome.
Renard D, Larue A, Taieb G, Jeanjean L, Labauge P. Renard D, et al. Among authors: jeanjean l. Clin Neurol Neurosurg. 2012 Sep;114(7):1019-20. doi: 10.1016/j.clineuro.2012.01.024. Epub 2012 Feb 17. Clin Neurol Neurosurg. 2012. PMID: 22342818 No abstract available.
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.
15 results