1. M. Gargiulo, S. Lejeune, M. L. Tanguy, K. Lahlou-Laforet, A. Faudet, D. Cohen, J. Feingold, and A. Durr. Long-term outcome of presymptomatic testing in Huntington disease. Eur J Hum Genet, 17(2):165-71, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglandEjhg. [WWW] Keyword(s): Depression/therapy, *Genetic Counseling, Genetic Predisposition to Disease/*psychology, Genetic Screening/*psychology, Humans, Huntington Disease/*diagnosis/genetics/*psychology, Interviews as Topic, Multivariate Analysis.



2. D. Lorenz, S. Klebe, G. Stevanin, S. Thier, A. Nebel, J. Feingold, H. Frederiksen, E. Denis, K. Christensen, S. Schreiber, A. Brice, G. Deuschl, and A. Durr. Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients. Eur J Hum Genet, 17(6):766-73, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglandEjhg. [WWW] Keyword(s): Adolescent, Adult, Aged, Aged, 80 and over, Denmark, Essential Tremor/ethnology/*genetics, European Continental Ancestry Group/genetics, Female, France, Genetic Variation, Genotype, Germany, Humans, Linkage (Genetics), Male, Middle Aged, Pedigree, Receptors, Dopamine D3/*genetics.



3. A. Camuzat, M. Romana, A. Durr, J. Feingold, A. Brice, M. Ruberg, and A. Lannuzel. The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism. Mov Disord, 23(16):2384-91, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Aged, Case-Control Studies, Chi-Square Distribution, European Continental Ancestry Group, Female, Gene Frequency, Genotype, Guadeloupe/epidemiology, Humans, Linkage Disequilibrium, Male, Middle Aged, Parkinsonian Disorders/complications/*genetics, Polymorphism, Single Nucleotide/*genetics, Supranuclear Palsy, Progressive/complications/*genetics, tau Proteins/*classification/*genetics.



4. D. Lorenz, S. Klebe, G. Stevanin, S. Thier, A. Nebel, J. Feingold, H. Frederiksen, E. Denis, K. Christensen, S. Schreiber, A. Brice, G. Deuschl, and A. Durr. Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients. Eur J Hum Genet, 2008. Note: Journal articleEjhg. [WWW]



5. F. Mochel, P. Charles, F. Seguin, J. Barritault, C. Coussieu, L. Perin, Y. Le Bouc, C. Gervais, G. Carcelain, A. Vassault, J. Feingold, D. Rabier, and A. Durr. Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression. PLoS ONE, 2(7):e647, 2007. Note: Journal ArticleUnited States. [WWW]



6. A. Durr, M. Gargiulo, and J. Feingold. [Predictive testing: presymptomatic diagnosis in neurogenetic disorders]. Med Sci (Paris), 21(11):934-9, 2005. Note: English AbstractJournal ArticleReviewFranceM/s. [WWW] Keyword(s): Adult, Alzheimer Disease/diagnosis/genetics/prevention & control, Attitude to Health, Carrier State/diagnosis/psychology, Female, France, Genetic Screening/psychology, Heredodegenerative Disorders, Nervous, System/*diagnosis/genetics/psychology/therapy, Humans, Huntington Disease/diagnosis/genetics/psychology/therapy, Interdisciplinary Communication, Male, Medical Futility/psychology, Patient Care Team, Physician-Patient Relations, Predictive Value of Tests, Pregnancy, Prenatal Diagnosis.



7. M. Tazir, H. Azzedine, S. Assami, P. Sindou, S. Nouioua, R. Zemmouri, T. Hamadouche, M. Chaouch, J. Feingold, J. M. Vallat, E. Leguern, and D. Grid. Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C. Brain, 127(Pt 1):154-63, 2004. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Charcot-Marie-Tooth Disease/*genetics/pathology/physiopathology, Child, Chromosomes, Human, Pair 1/genetics, Disease Progression, Female, Genes, Recessive, Humans, Lamin Type A/*genetics, Male, Median Nerve/physiopathology, *Mutation, Nerve Fibers, Myelinated/pathology, Nerve Fibers, Unmyelinated/pathology, Neural Conduction, Phenotype.

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