P. Ibáñez

发表

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Patrizia Rizzu, Vincenzo Bonifati, Elmar Krieger, 2002, Science.

Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism

Y. Agid, P. Pollak, P. Heutink, 2003, Neurology.

Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.

A. Dürr, A. Leutenegger, A. Brice, 2006, Archives of neurology.

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.

Stéphane Thobois, Yves Agid, Pablo Ibáñez, 2006, Brain : a journal of neurology.

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

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

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease.

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

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century.

A. Dürr, A. Leutenegger, A. Brice, 2005, American journal of human genetics.

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

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

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.

Santiago Canals, S. Canals, A. Brice, 2003, Human molecular genetics.

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.

A. Destée, S. Heath, Y. Agid, 2009, Archives of neurology.

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

Y. Agid, A. Bonnet, P. Pollak, 2005, Annals of neurology.

Parkinson's disease: from causes to mechanisms.

M. Ruberg, A. Brice, F. Darios, 2005, Comptes rendus biologies.

Phenotype/genotype correlations in Parkinson's disease

A. Durr, A. Brice, S. Lesage, 2005 .