Pierre Pollak

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

A Dürr, Y Agid, Y. Agid, 2004, The Lancet.

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2017, Brain : a journal of neurology.

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

D. Hernandez, M. Nalls, A. Singleton, 2013, Human molecular genetics.

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Y. Agid, P. Pollak, A. Dürr, 2004, Neurology.

BROMOCRIPTINE ASSOCIATED WITH A PERIPHERAL DOPAMINE BLOCKING AGENT IN TREATMENT OF PARKINSON'S DISEASE

Y. Agid, A. Bonnet, J. Signoret, 1979, The Lancet.

FXTAS: New Insights and the Need for Revised Diagnostic Criteria (S20.006)

D. Maltête, S. Thobois, M. Anheim, 2013, Neurology.

Congenital mirror movements: Mutational analysis of RAD51 and DCC in 26 cases

S. Rossi, L. Defebvre, M. Vidailhet, 2014, Neurology.