A Dürr

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Second consensus statement on the diagnosis of multiple system atrophy

P Sandroni, P A Low, N Quinn, 2008, Neurology.

Clinical and genetic abnormalities in patients with Friedreich's ataxia.

A Dürr, Y Agid, Y. Agid, 1996, The New England journal of medicine.

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

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

[18F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations

A Dürr, P. Pollak, P. Remy, 2000, Neurology.

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

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

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.

A Dürr, Y. Agid, A. Durr, 1995, Brain : a journal of neurology.

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

P Trouillas, A Dürr, M. Koenig, 1999, Annals of neurology.

Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.

A Dürr, Y Agid, E. Hirsch, 1998, Human molecular genetics.

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Bonifati, N W Wood, A Dürr, 2000, The New England journal of medicine.

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.

P Trouillas, A Dürr, S J Kish, 1997, Human molecular genetics.

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I

A Dürr, Y Agid, Y. Agid, 1998, Annals of neurology.