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Page 1
Neuroendocrine disturbances in Huntington's disease.
Saleh N, Moutereau S, Durr A, Krystkowiak P, Azulay JP, Tranchant C, Broussolle E, Morin F, Bachoud-Lévi AC, Maison P. Saleh N, et al. Among authors: durr a. PLoS One. 2009;4(3):e4962. doi: 10.1371/journal.pone.0004962. Epub 2009 Mar 25. PLoS One. 2009. PMID: 19319184 Free PMC article.
How much phenotypic variation can be attributed to parkin genotype?
Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destée A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Lohmann E, et al. Among authors: durr a. Ann Neurol. 2003 Aug;54(2):176-85. doi: 10.1002/ana.10613. Ann Neurol. 2003. PMID: 12891670
Spinocerebellar ataxia with sensory neuropathy (SCA25).
Stevanin G, Broussolle E, Streichenberger N, Kopp N, Brice A, Durr A. Stevanin G, et al. Among authors: durr a. Cerebellum. 2005;4(1):58-61. doi: 10.1080/14734220510007932. Cerebellum. 2005. PMID: 15895562
Rapid eye movement sleep disturbances in Huntington disease.
Arnulf I, Nielsen J, Lohmann E, Schiefer J, Wild E, Jennum P, Konofal E, Walker M, Oudiette D, Tabrizi S, Durr A. Arnulf I, et al. Among authors: durr a. Arch Neurol. 2008 Apr;65(4):482-8. doi: 10.1001/archneur.65.4.482. Arch Neurol. 2008. PMID: 18413470
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.
A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
Lohmann E, Thobois S, Lesage S, Broussolle E, du Montcel ST, Ribeiro MJ, Remy P, Pelissolo A, Dubois B, Mallet L, Pollak P, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group. Lohmann E, et al. Neurology. 2009 Jan 13;72(2):110-6. doi: 10.1212/01.wnl.0000327098.86861.d4. Epub 2008 Nov 5. Neurology. 2009. PMID: 18987353 Free PMC article.
766 results