Durr A - Search Results

1

Long-term outcome of presymptomatic testing in Huntington disease.

Gargiulo M, Lejeune S, Tanguy ML, Lahlou-Laforêt K, Faudet A, Cohen D, Feingold J, Durr A. Gargiulo M, et al. Among authors: durr a. Eur J Hum Genet. 2009 Feb;17(2):165-71. doi: 10.1038/ejhg.2008.146. Epub 2008 Aug 20. Eur J Hum Genet. 2009. PMID: 18716614 Free PMC article.

2

Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes.

Pêcheux C, Mouret JF, Dürr A, Agid Y, Feingold J, Brice A, Dodé C, Kaplan JC. Pêcheux C, et al. Among authors: durr a. J Med Genet. 1995 May;32(5):399-400. doi: 10.1136/jmg.32.5.399. J Med Genet. 1995. PMID: 7616551 Free PMC article.

3

Diagnosis of "sporadic" Huntington's disease.

Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A. Dürr A, et al. J Neurol Sci. 1995 Mar;129(1):51-5. doi: 10.1016/0022-510x(94)00250-r. J Neurol Sci. 1995. PMID: 7751845

4

Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.

Dodé C, Dürr A, Pêcheux C, Mouret JF, Belal S, Bachner L, Agid Y, Kaplan JC, Brice A, Feingold J. Dodé C, et al. Among authors: durr a. C R Acad Sci III. 1993 Nov;316(11):1374-80. C R Acad Sci III. 1993. PMID: 8087617

5

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity.

Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A. Dürr A, et al. Brain. 1993 Dec;116 ( Pt 6):1497-508. doi: 10.1093/brain/116.6.1497. Brain. 1993. PMID: 8293283

6

[Chorea and Huntington's disease].

Dürr A. Dürr A. Rev Prat. 1997 May 15;47(10):1083-7. Rev Prat. 1997. PMID: 9208671 French.

7

[Presymptomatic diagnosis in genetics: the model of Huntington disease].

Feingold J, Dürr A. Feingold J, et al. Among authors: durr a. Pathol Biol (Paris). 1997 Mar;45(3):209-12. Pathol Biol (Paris). 1997. PMID: 9296065 French.

8

Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers.

Hahn-Barma V, Deweer B, Dürr A, Dodé C, Feingold J, Pillon B, Agid Y, Brice A, Dubois B. Hahn-Barma V, et al. Among authors: durr a. J Neurol Neurosurg Psychiatry. 1998 Feb;64(2):172-7. doi: 10.1136/jnnp.64.2.172. J Neurol Neurosurg Psychiatry. 1998. PMID: 9489526 Free PMC article. Clinical Trial.

9

Homozygosity in Huntington's disease.

Dürr A, Hahn-Barma V, Brice A, Pêcheux C, Dodé C, Feingold J. Dürr A, et al. J Med Genet. 1999 Feb;36(2):172-3. J Med Genet. 1999. PMID: 10051023 Free PMC article. No abstract available.

10

Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology.

Stevanin G, Dürr A, Brice A. Stevanin G, et al. Among authors: durr a. Eur J Hum Genet. 2000 Jan;8(1):4-18. doi: 10.1038/sj.ejhg.5200403. Eur J Hum Genet. 2000. PMID: 10713882 Review.

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