Tranchant C - Search Results

1

[Peripheral neuropathies associated with hereditary cerebellar ataxias].

Anheim M, Tranchant C. Anheim M, et al. Among authors: tranchant c. Rev Neurol (Paris). 2011 Jan;167(1):72-6. doi: 10.1016/j.neurol.2010.07.041. Epub 2010 Dec 30. Rev Neurol (Paris). 2011. PMID: 21195440 Review. French.

2

[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].

Degos B, Echaniz-Laguna A, Latour P, Vandenberghe A, Anheim M, Talmant V, Tranchant C. Degos B, et al. Among authors: tranchant c. Rev Neurol (Paris). 2004 Dec;160(12):1203-6. doi: 10.1016/s0035-3787(04)71168-6. Rev Neurol (Paris). 2004. PMID: 15602369 French.

3

[Pure trigeminal motor neuropathy presenting with temporo-mandibular joint dysfunction in a patient with HIV and HCV infections].

Anheim M, Echaniz-Laguna A, Rey D, Tranchant C. Anheim M, et al. Among authors: tranchant c. Rev Neurol (Paris). 2006 Jan;162(1):92-4. doi: 10.1016/s0035-3787(06)74987-6. Rev Neurol (Paris). 2006. PMID: 16446628 French.

4

[Ataxia associated with gluten sensitivity, myth or reality?].

Anheim M, Degos B, Echaniz-Laguna A, Fleury M, Grucker M, Tranchant C. Anheim M, et al. Among authors: tranchant c. Rev Neurol (Paris). 2006 Feb;162(2):214-21. doi: 10.1016/s0035-3787(06)75002-0. Rev Neurol (Paris). 2006. PMID: 16518262 French.

5

[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].

Anheim M, Chaigne D, Fleury M, Santorelli FM, De Sèze J, Durr A, Brice A, Koenig M, Tranchant C. Anheim M, et al. Among authors: tranchant c. Rev Neurol (Paris). 2008 Apr;164(4):363-8. doi: 10.1016/j.neurol.2008.02.001. Epub 2008 Mar 25. Rev Neurol (Paris). 2008. PMID: 18439928 French.

6

Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.

Anheim M, Fleury M, Monga B, Laugel V, Chaigne D, Rodier G, Ginglinger E, Boulay C, Courtois S, Drouot N, Fritsch M, Delaunoy JP, Stoppa-Lyonnet D, Tranchant C, Koenig M. Anheim M, et al. Among authors: tranchant c. Neurogenetics. 2010 Feb;11(1):1-12. doi: 10.1007/s10048-009-0196-y. Epub 2009 May 14. Neurogenetics. 2010. PMID: 19440741

7

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.

8

Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.

Gebus O, Montaut S, Monga B, Wirth T, Cheraud C, Alves Do Rego C, Zinchenko I, Carré G, Hamdaoui M, Hautecloque G, Nguyen-Them L, Lannes B, Chanson JB, Lagha-Boukbiza O, Fleury MC, Devys D, Nicolas G, Rudolf G, Bereau M, Mallaret M, Renaud M, Acquaviva C, Koenig M, Koob M, Kremer S, Namer IJ, Cazeneuve C, Echaniz-Laguna A, Tranchant C, Anheim M. Gebus O, et al. Among authors: tranchant c. J Neurol. 2017 Jun;264(6):1118-1126. doi: 10.1007/s00415-017-8500-5. Epub 2017 May 6. J Neurol. 2017. PMID: 28478596

9

CANVAS: A very late onset cerebellar ataxia, due to biallelic expansions in the RFC1 gene.

Tranchant C, Anheim M. Tranchant C, et al. Rev Neurol (Paris). 2019 Oct;175(9):493-494. doi: 10.1016/j.neurol.2019.05.002. Epub 2019 Sep 13. Rev Neurol (Paris). 2019. PMID: 31526553 No abstract available.

10

[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy].

Echaniz-Laguna A, Rousso E, Anheim M, Fleury M, Cossée M, Tranchant C. Echaniz-Laguna A, et al. Among authors: tranchant c. Rev Neurol (Paris). 2005 Apr;161(4):437-44. doi: 10.1016/s0035-3787(05)85073-8. Rev Neurol (Paris). 2005. PMID: 15924079 French.

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