Author / Editor

• Lesage, Suzanne (10)
• Durr, Alexandra (9)
• Vidailhet, Marie (8)
• Pollak, Pierre (7)
• Damier, Philippe (6)
• Dürr, Alexandra (6)
• Lohmann, Ebba (6)
• Hardy, John (5)
• Martinez, Maria (5)
• Picard, Fabienne (5)
• Saad, Mohamad (5)
• Tison, François (5)
• Anheim, Mathieu (4)
• Condroyer, Christel (4)
• Durif, Franck (4)
• Gasser, Thomas (4)
• Heutink, Peter (4)
• Ouvrard-Hernandez, Anne-Marie (4)
• Singleton, Andrew B (4)
• Clot, Fabienne (3)
• Corvol, Jean-Christophe (3)
• Forlani, Sylvie (3)
• Grabli, David (3)
• Hernandez, Dena G (3)
• LeGuern, Eric (3)
• Nalls, Michael A (3)
• Roze, Emmanuel (3)
• Schulte, Claudia (3)
• Sharma, Manu (3)

Document type

• Article scientifique (19)

Full text accessibility

• Restricted access (10)
• Free access (8)

Full text version

• Published version (15)
• Unknown (2)
• Accepted version (1)
• No fulltext (1)

Licence

• CC BY-NC (1)

Subject

• Humans (18)
• Adult (14)
• Male (14)
• Female (13)
• Middle aged (13)
• Aged (12)
• Age of onset (7)
• Genetic predisposition to disease (6)
• Adolescent (5)
• Parkinson disease/genetics (5)
• Aged, 80 and over (4)
• Child (4)
• Child, preschool (4)
• European continental ancestry group/genetics (4)
• Genome-wide association study (4)
• Genotype (4)
• Pedigree (4)
• Dna mutational analysis (3)
• France (3)
• Genetic predisposition to disease/genetics (3)
• Mutation (3)
• Mutation/genetics (3)
• Polymorphism, single nucleotide (3)
• Polymorphism, single nucleotide/genetics (3)
• Young adult (3)
• Alleles (2)
• Case-control studies (2)
• Chromosome mapping (2)
• Family health (2)
• Follow-up studies (2)