Lezin A - Search Results

1

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.

Cancel G, Dürr A, Didierjean O, Imbert G, Bürk K, Lezin A, Belal S, Benomar A, Abada-Bendib M, Vial C, Guimarães J, Chneiweiss H, Stevanin G, Yvert G, Abbas N, Saudou F, Lebre AS, Yahyaoui M, Hentati F, Vernant JC, Klockgether T, Mandel JL, Agid Y, Brice A. Cancel G, et al. Among authors: lezin a. Hum Mol Genet. 1997 May;6(5):709-15. doi: 10.1093/hmg/6.5.709. Hum Mol Genet. 1997. PMID: 9158145

2

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.

Lezin A, Cancel G, Stevanin G, Smadja D, Vernant JC, Dürr A, Martial J, Buisson GG, Bellance R, Chneiweiss H, Agid Y, Brice A. Lezin A, et al. Hum Genet. 1996 May;97(5):671-6. doi: 10.1007/BF02281881. Hum Genet. 1996. PMID: 8655151

3

Linkage disequilibrium at the SCA2 locus.

Didierjean O, Cancel G, Stevanin G, Dürr A, Bürk K, Benomar A, Lezin A, Belal S, Abada-Bendid M, Klockgether T, Brice A. Didierjean O, et al. Among authors: lezin a. J Med Genet. 1999 May;36(5):415-7. J Med Genet. 1999. PMID: 10353790 Free PMC article.

4

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.

Dürr A, Smadja D, Cancel G, Lezin A, Stevanin G, Mikol J, Bellance R, Buisson GG, Chneiweiss H, Dellanave J, et al. Dürr A, et al. Among authors: lezin a. Brain. 1995 Dec;118 ( Pt 6):1573-81. doi: 10.1093/brain/118.6.1573. Brain. 1995. PMID: 8595486

5

[Involvements of the peripheral nervous system and skeletal muscles in HTLV1-related paraplegia. Study of 70 cases seen in Martinique].

Smadja D, Bellance R, Cabre P, Kerjean J, Lezin A, Vernant JC. Smadja D, et al. Among authors: lezin a. Rev Neurol (Paris). 1995 Mar;151(3):190-5. Rev Neurol (Paris). 1995. PMID: 7676155 French.

6

Seroindeterminate patterns and seroconversions to human T-lymphotropic virus type I positivity in blood donors from Martinique, French West Indies.

Césaire R, Bera O, Maier H, Lezin A, Martial J, Ouka M, Kerob-Bauchet B, Ould Amar AK, Vernant JC. Césaire R, et al. Among authors: lezin a. Transfusion. 1999 Oct;39(10):1145-9. doi: 10.1046/j.1537-2995.1999.39101145.x. Transfusion. 1999. PMID: 10532611

7

HTLV-1 proviral load in peripheral blood mononuclear cells quantified in 100 HAM/TSP patients: a marker of disease progression.

Olindo S, Lézin A, Cabre P, Merle H, Saint-Vil M, Edimonana Kaptue M, Signate A, Césaire R, Smadja D. Olindo S, et al. Among authors: lezin a. J Neurol Sci. 2005 Oct 15;237(1-2):53-9. doi: 10.1016/j.jns.2005.05.010. J Neurol Sci. 2005. PMID: 15972218

8

Absence of consistent association between human leukocyte antigen-I and -II alleles and human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis risk in an HTLV-1 French Afro-Caribbean population.

Deschamps R, Béra O, Belrose G, Lezin A, Bellance R, Signate A, Cabre P, Smadja D, Césaire R, Olindo S. Deschamps R, et al. Among authors: lezin a. Int J Infect Dis. 2010 Nov;14(11):e986-90. doi: 10.1016/j.ijid.2010.05.020. Epub 2010 Sep 17. Int J Infect Dis. 2010. PMID: 20851016 Free article.

9

Natural history of human T-lymphotropic virus 1-associated myelopathy: a 14-year follow-up study.

Olindo S, Cabre P, Lézin A, Merle H, Saint-Vil M, Signate A, Bonnan M, Chalon A, Magnani L, Cesaire R, Smadja D. Olindo S, et al. Among authors: lezin a. Arch Neurol. 2006 Nov;63(11):1560-6. doi: 10.1001/archneur.63.11.1560. Arch Neurol. 2006. PMID: 17101824

10

Human T lymphotropic virus type I (HTLV-I) proviral load in cerebrospinal fluid: a new criterion for the diagnosis of HTLV-I-associated myelopathy/tropical spastic paraparesis?

Lezin A, Olindo S, Oliere S, Varrin-Doyer M, Marlin R, Cabre P, Smadja D, Cesaire R. Lezin A, et al. J Infect Dis. 2005 Jun 1;191(11):1830-4. doi: 10.1086/429962. Epub 2005 Apr 28. J Infect Dis. 2005. PMID: 15871115

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