| | Title | Authors / Editors | Date |
|
unige:20058 |
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations |
Ribeiro, Maria-Joao; Thobois, Stéphane; Lohmann, Ebba; du Montcel, S. T.; ... Remy, P. |
2009 |
|
unige:45179 |
Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms |
Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis |
2009 |
|
unige:19175 |
Are parkin patients particularly suited for deep-brain stimulation? |
Lohmann, Ebba; Welter, Marie-Laure; Fraix, Valerie; Krack, Paul; ... Brice, Alexis |
2008 |
|
unige:45192 |
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? |
Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis |
2012 |
|
unige:32873 |
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population |
Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis |
2011 |
|
unige:32874 |
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease |
Lesage, Suzanne; Anheim, Mathieu; Condroyer, Christel; Pollak, Pierre; ... Brice, Alexis |
2011 |
|
unige:32884 |
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans |
Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis |
2010 |
Lohmann, Ebba
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