Alexandra D�rr

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

Mireille Coss�e, Alexandra D�rr, Mich�le Schmitt et al. · Annals of Neurology · 1999 · 382 citations

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

Hiroto Fujigasaki, Ishwar C. Verma, A. Camuzat et al. · Annals of Neurology · 2001 · 103 citations

Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation

Nathalie Kubis, Alexandra D�rr, Michel Gugenheim et al. · Muscle & Nerve · 1999 · 50 citations

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

Annette Abel, Núria Fonknechten, Anne Höfer et al. · Neurogenetics · 2004 · 49 citations

Genetic Disorder, Medicine, Genetics +4

PARK6 is a common cause of familial parkinsonism

Enza Maria Valente, Francesco Brancati, Viviana Caputo et al. · Neurological Sciences · 2002 · 40 citations

Neurological Disorder, Parkinson Disease, Motor Disorder +5