Tranchant C - Search Results

1

Is Motor Side Onset of Parkinson's Disease a Risk Factor for Developing Impulsive-Compulsive Behavior? A Cross-Sectional Study.

Phillipps C, Longato N, Béreau M, Carrière N, Lagha-Boukbiza O, Mengin AC, Monga B, Defebvre L, Ory-Magne F, Castrioto A, Lhommée E, Rascol O, Krack P, Tranchant C, Corvol JC, Anheim M. Phillipps C, et al. Among authors: tranchant c. Mov Disord. 2020 Jun;35(6):1080-1081. doi: 10.1002/mds.28053. Epub 2020 Apr 20. Mov Disord. 2020. PMID: 32311121 No abstract available.

2

Movement disorders in multiple sclerosis.

Tranchant C, Bhatia KP, Marsden CD. Tranchant C, et al. Mov Disord. 1995 Jul;10(4):418-23. doi: 10.1002/mds.870100403. Mov Disord. 1995. PMID: 7565820 Review.

3

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Anheim M, Fleury MC, Franques J, Moreira MC, Delaunoy JP, Stoppa-Lyonnet D, Koenig M, Tranchant C. Anheim M, et al. Among authors: tranchant c. Arch Neurol. 2008 Jul;65(7):958-62. doi: 10.1001/archneur.65.7.958. Arch Neurol. 2008. PMID: 18625865

4

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.

5

SPG11 spastic paraplegia. A new cause of juvenile parkinsonism.

Anheim M, Lagier-Tourenne C, Stevanin G, Fleury M, Durr A, Namer IJ, Denora P, Brice A, Mandel JL, Koenig M, Tranchant C. Anheim M, et al. Among authors: tranchant c. J Neurol. 2009 Jan;256(1):104-8. doi: 10.1007/s00415-009-0083-3. Epub 2009 Feb 9. J Neurol. 2009. PMID: 19224311

6

[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.

7

Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases.

Marcel C, Anheim M, Flamand-Rouvière C, Heran F, Masnou P, Boulay C, Mari I, Tranchant C, Roze E. Marcel C, et al. Among authors: tranchant c. J Neurol. 2010 Aug;257(8):1369-72. doi: 10.1007/s00415-010-5534-3. Epub 2010 Mar 30. J Neurol. 2010. PMID: 20352251

8

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

9

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.

10

[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.

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