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

Year Number of Results
1985 1
1987 2
1988 2
1989 2
1990 8
1991 9
1992 6
1993 9
1994 4
1995 5
1996 4
1997 2
1998 3
1999 3
2000 9
2001 6
2002 6
2003 4
2004 11
2005 10
2006 16
2007 12
2008 13
2009 19
2010 17
2011 8
2012 12
2013 11
2014 16
2015 11
2016 19
2017 20
2018 15
2019 14
2020 22
2021 11
Text availability
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Article type
Publication date

Search Results

316 results
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Page 1
Movement disorders in mitochondrial diseases.
Tranchant C, Anheim M. Tranchant C, et al. Rev Neurol (Paris). 2016 Aug-Sep;172(8-9):524-529. doi: 10.1016/j.neurol.2016.07.003. Epub 2016 Jul 28. Rev Neurol (Paris). 2016. PMID: 27476418 Review.
Parkinsonian-Pyramidal syndromes: A systematic review.
Tranchant C, Koob M, Anheim M. Tranchant C, et al. Parkinsonism Relat Disord. 2017 Jun;39:4-16. doi: 10.1016/j.parkreldis.2017.02.025. Epub 2017 Feb 22. Parkinsonism Relat Disord. 2017. PMID: 28256436 Review.
Foreword.
Tranchant C. Tranchant C. Rev Neurol (Paris). 2019 Sep-Oct;175(7-8):415-416. doi: 10.1016/j.neurol.2019.08.001. Rev Neurol (Paris). 2019. PMID: 31519226 No abstract available.
Foreword.
Azulay JP, Durif F, Vidailhet M, Tranchant C. Azulay JP, et al. Among authors: tranchant c. Rev Neurol (Paris). 2018 Nov;174(9):579-580. doi: 10.1016/j.neurol.2018.10.001. Rev Neurol (Paris). 2018. PMID: 30343834 No abstract available.
Increased diagnostic yield in complex dystonia through exome sequencing.
Wirth T, Tranchant C, Drouot N, Keren B, Mignot C, Cif L, Lefaucheur R, Lion-François L, Méneret A, Gras D, Roze E, Laroche C, Burbaud P, Bannier S, Lagha-Boukbiza O, Spitz MA, Laugel V, Bereau M, Ollivier E, Nitschke P, Doummar D, Rudolf G, Anheim M, Chelly J. Wirth T, et al. Among authors: tranchant c. Parkinsonism Relat Disord. 2020 May;74:50-56. doi: 10.1016/j.parkreldis.2020.04.003. Epub 2020 Apr 20. Parkinsonism Relat Disord. 2020. PMID: 32334381
[Foreword].
Verny C, Tranchant C. Verny C, et al. Among authors: tranchant c. Rev Neurol (Paris). 2014 May;170(5):307-8. doi: 10.1016/j.neurol.2014.04.003. Rev Neurol (Paris). 2014. PMID: 24838086 French. No abstract available.
Éditorial.
Azulay JP, Tranchant C. Azulay JP, et al. Among authors: tranchant c. Presse Med. 2017 Mar;46(2 Pt 1):174. doi: 10.1016/j.lpm.2017.02.001. Presse Med. 2017. PMID: 28325375 French. No abstract available.
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Roux T, Barbier M, Papin M, Davoine CS, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C, Goizet C, Klebe S, Lohmann E, Van Maldergem L, van Broeckhoven C, Coutelier M, Tesson C, Stevanin G, Duyckaerts C, Brice A, Durr A; SPATAX network. Roux T, et al. Among authors: tranchant c. Genet Med. 2020 Nov;22(11):1851-1862. doi: 10.1038/s41436-020-0899-x. Epub 2020 Jul 27. Genet Med. 2020. PMID: 32713943
Early onset collagen VI myopathies: Genetic and clinical correlations.
Briñas L, Richard P, Quijano-Roy S, Gartioux C, Ledeuil C, Lacène E, Makri S, Ferreiro A, Maugenre S, Topaloglu H, Haliloglu G, Pénisson-Besnier I, Jeannet PY, Merlini L, Navarro C, Toutain A, Chaigne D, Desguerre I, de Die-Smulders C, Dunand M, Echenne B, Eymard B, Kuntzer T, Maincent K, Mayer M, Plessis G, Rivier F, Roelens F, Stojkovic T, Taratuto AL, Lubieniecki F, Monges S, Tranchant C, Viollet L, Romero NB, Estournet B, Guicheney P, Allamand V. Briñas L, et al. Among authors: tranchant c. Ann Neurol. 2010 Oct;68(4):511-20. doi: 10.1002/ana.22087. Ann Neurol. 2010. PMID: 20976770
[Myasthenia].
Fleury-Lesaunier MC, Tranchant C. Fleury-Lesaunier MC, et al. Among authors: tranchant c. Rev Prat. 2013 Jan;63(1):109-12. Rev Prat. 2013. PMID: 23457841 Review. French. No abstract available.
316 results
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