Tranchant C - Search Results

1

Imbalanced motivated behaviors according to motor sign asymmetry in drug-naïve Parkinson's disease.

Béreau M, Castrioto A, Servant M, Lhommée E, Desmarets M, Bichon A, Pélissier P, Schmitt E, Klinger H, Longato N, Phillipps C, Wirth T, Fraix V, Benatru I, Durif F, Azulay JP, Moro E, Broussolle E, Thobois S, Tranchant C, Krack P, Anheim M. Béreau M, et al. Among authors: tranchant c. Sci Rep. 2023 Dec 1;13(1):21234. doi: 10.1038/s41598-023-48188-0. Sci Rep. 2023. PMID: 38040775 Free PMC article.

2

Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study.

Bensimon G, Ludolph A, Agid Y, Vidailhet M, Payan C, Leigh PN; NNIPPS Study Group. Bensimon G, et al. Brain. 2009 Jan;132(Pt 1):156-71. doi: 10.1093/brain/awn291. Epub 2008 Nov 23. Brain. 2009. PMID: 19029129 Free PMC article. Clinical Trial.

3

Neuroendocrine disturbances in Huntington's disease.

Saleh N, Moutereau S, Durr A, Krystkowiak P, Azulay JP, Tranchant C, Broussolle E, Morin F, Bachoud-Lévi AC, Maison P. Saleh N, et al. Among authors: tranchant c. PLoS One. 2009;4(3):e4962. doi: 10.1371/journal.pone.0004962. Epub 2009 Mar 25. PLoS One. 2009. PMID: 19319184 Free PMC article.

4

[Autosomal recessive cerebellar ataxias].

Tranchant C, Anheim M. Tranchant C, et al. Presse Med. 2009 Dec;38(12):1852-9. doi: 10.1016/j.lpm.2009.01.025. Epub 2009 May 12. Presse Med. 2009. PMID: 19442480 Review. French.

5

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.

Lesage S, Anheim M, Condroyer C, Pollak P, Durif F, Dupuits C, Viallet F, Lohmann E, Corvol JC, Honoré A, Rivaud S, Vidailhet M, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Hum Mol Genet. 2011 Jan 1;20(1):202-10. doi: 10.1093/hmg/ddq454. Epub 2010 Oct 14. Hum Mol Genet. 2011. PMID: 20947659

6

Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa.

Lesage S, Condroyer C, Hecham N, Anheim M, Belarbi S, Lohman E, Viallet F, Pollak P, Abada M, Dürr A, Tazir M, Brice A; French Parkinson Disease Genetic Group. Lesage S, et al. Neurology. 2011 Jan 18;76(3):301-3. doi: 10.1212/WNL.0b013e318207b01e. Neurology. 2011. PMID: 21242499 No abstract available.

7

[Sudden onset sensorimotor deficit: first consider stroke].

Tranchant C, Anheim M. Tranchant C, et al. Rev Prat. 2011 Oct;61(8):1130. Rev Prat. 2011. PMID: 22135984 French. No abstract available.

8

The autosomal recessive cerebellar ataxias.

Anheim M, Tranchant C, Koenig M. Anheim M, et al. Among authors: tranchant c. N Engl J Med. 2012 Feb 16;366(7):636-46. doi: 10.1056/NEJMra1006610. N Engl J Med. 2012. PMID: 22335741 Review. No abstract available.

9

Heterogeneity and frequency of movement disorders in juvenile and adult-onset Niemann-Pick C disease.

Anheim M, Lagha-Boukbiza O, Fleury-Lesaunier MC, Valenti-Hirsch MP, Hirsch E, Gervais-Bernard H, Broussolle E, Thobois S, Vanier MT, Latour P, Tranchant C. Anheim M, et al. Among authors: tranchant c. J Neurol. 2014 Jan;261(1):174-9. doi: 10.1007/s00415-013-7159-9. Epub 2013 Nov 1. J Neurol. 2014. PMID: 24178705

10

SPG15: a cause of juvenile atypical levodopa responsive parkinsonism.

Mallaret M, Lagha-Boukbiza O, Biskup S, Namer IJ, Rudolf G, Anheim M, Tranchant C. Mallaret M, et al. Among authors: tranchant c. J Neurol. 2014 Feb;261(2):435-7. doi: 10.1007/s00415-013-7216-4. Epub 2013 Dec 24. J Neurol. 2014. PMID: 24366652 No abstract available.

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