Durr A - Search Results

1

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Moss DJH, Pardiñas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S; TRACK-HD investigators; REGISTRY investigators; Holmans P, Jones L, Tabrizi SJ. Moss DJH, et al. Among authors: durr a. Lancet Neurol. 2017 Sep;16(9):701-711. doi: 10.1016/S1474-4422(17)30161-8. Epub 2017 Jun 20. Lancet Neurol. 2017. PMID: 28642124

2

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.

3

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

Vaughan J, Durr A, Tassin J, Bereznai B, Gasser T, Bonifati V, De Michele G, Fabrizio E, Volpe G, Bandmann O, Johnson WG, Golbe LI, Breteler M, Meco G, Agid Y, Brice A, Marsden CD, Wood NW. Vaughan J, et al. Among authors: durr a. Ann Neurol. 1998 Aug;44(2):270-3. doi: 10.1002/ana.410440221. Ann Neurol. 1998. PMID: 9708553

4

PARK6-linked parkinsonism occurs in several European families.

Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, Caputo V, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease. Valente EM, et al. Among authors: durr a. Ann Neurol. 2002 Jan;51(1):14-8. Ann Neurol. 2002. PMID: 11782979

5

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Stevanin G, Camuzat A, Holmes SE, Julien C, Sahloul R, Dodé C, Hahn-Barma V, Ross CA, Margolis RL, Durr A, Brice A. Stevanin G, et al. Among authors: durr a. Neurology. 2002 Mar 26;58(6):965-7. doi: 10.1212/wnl.58.6.965. Neurology. 2002. PMID: 11914418

6

Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.

Evers-Kiebooms G, Nys K, Harper P, Zoeteweij M, Dürr A, Jacopini G, Yapijakis C, Simpson S. Evers-Kiebooms G, et al. Among authors: durr a. Eur J Hum Genet. 2002 Mar;10(3):167-76. doi: 10.1038/sj.ejhg.5200781. Eur J Hum Genet. 2002. PMID: 11973620

7

Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxia.

Lesca G, Goizet C, Dürr A. Lesca G, et al. Among authors: durr a. J Med Genet. 2002 Jul;39(7):522-5. doi: 10.1136/jmg.39.7.522. J Med Genet. 2002. PMID: 12114488 Free PMC article. No abstract available.

8

Prenatal testing for Huntington's disease: a European collaborative study.

Simpson SA, Zoeteweij MW, Nys K, Harper P, Dürr A, Jacopini G, Yapijakis C, Evers-Kiebooms G. Simpson SA, et al. Among authors: durr a. Eur J Hum Genet. 2002 Nov;10(11):689-93. doi: 10.1038/sj.ejhg.5200871. Eur J Hum Genet. 2002. PMID: 12404099

9

Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxias.

Goizet C, Lesca G, Dürr A; French Group for Presymptomatic Testing in Neurogenetic Disorders. Goizet C, et al. Among authors: durr a. Neurology. 2002 Nov 12;59(9):1330-6. doi: 10.1212/01.wnl.0000032255.75650.c2. Neurology. 2002. PMID: 12427879

10

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism.

Rawal N, Periquet M, Lohmann E, Lücking CB, Teive HA, Ambrosio G, Raskin S, Lincoln S, Hattori N, Guimaraes J, Horstink MW, Dos Santos Bele W, Brousolle E, Destée A, Mizuno Y, Farrer M, Deleuze JF, De Michele G, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Rawal N, et al. Among authors: durr a. Neurology. 2003 Apr 22;60(8):1378-81. doi: 10.1212/01.wnl.0000056167.89221.be. Neurology. 2003. PMID: 12707451

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