Durr A - Search Results

1

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.

Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T, Vidailhet M, Doummar D. Gras D, et al. Among authors: durr a. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):956-62. doi: 10.1136/jnnp-2012-302505. Epub 2012 Jul 24. J Neurol Neurosurg Psychiatry. 2012. PMID: 22832740

2

Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlations.

Dubourg O, Dürr A, Cancel G, Stevanin G, Chneiweiss H, Penet C, Agid Y, Brice A. Dubourg O, et al. Among authors: durr a. Ann Neurol. 1995 Feb;37(2):176-80. doi: 10.1002/ana.410370207. Ann Neurol. 1995. PMID: 7847859

3

The phenotype of "pure" autosomal dominant spastic paraplegia.

Dürr A, Brice A, Serdaru M, Rancurel G, Derouesné C, Lyon-Caen O, Agid Y, Fontaine B. Dürr A, et al. Neurology. 1994 Jul;44(7):1274-7. doi: 10.1212/wnl.44.7.1274. Neurology. 1994. PMID: 8035929

4

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.

5

DYT1 mutation in French families with idiopathic torsion dystonia.

Lebre AS, Durr A, Jedynak P, Ponsot G, Vidailhet M, Agid Y, Brice A. Lebre AS, et al. Among authors: durr a. Brain. 1999 Jan;122 ( Pt 1):41-5. doi: 10.1093/brain/122.1.41. Brain. 1999. PMID: 10050893

6

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Brassat D, Camuzat A, Vidailhet M, Feki I, Jedynak P, Klap P, Agid Y, Dürr A, Brice A. Brassat D, et al. Among authors: durr a. Arch Neurol. 2000 Mar;57(3):333-5. doi: 10.1001/archneur.57.3.333. Arch Neurol. 2000. PMID: 10714658

7

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation.

Herman-Bert A, Stevanin G, Netter JC, Rascol O, Brassat D, Calvas P, Camuzat A, Yuan Q, Schalling M, Dürr A, Brice A. Herman-Bert A, et al. Among authors: durr a. Am J Hum Genet. 2000 Jul;67(1):229-35. doi: 10.1086/302958. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820125 Free PMC article.

8

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

Tassin J, Dürr A, Bonnet AM, Gil R, Vidailhet M, Lücking CB, Goas JY, Durif F, Abada M, Echenne B, Motte J, Lagueny A, Lacomblez L, Jedynak P, Bartholomé B, Agid Y, Brice A. Tassin J, et al. Among authors: durr a. Brain. 2000 Jun;123 ( Pt 6):1112-21. doi: 10.1093/brain/123.6.1112. Brain. 2000. PMID: 10825351

9

[18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations.

Broussolle E, Lücking CB, Ginovart N, Pollak P, Remy P, Dürr A. Broussolle E, et al. Among authors: durr a. Neurology. 2000 Sep 26;55(6):877-9. doi: 10.1212/wnl.55.6.877. Neurology. 2000. PMID: 10994015

10

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Among authors: durr a. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

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