R. Marconi

Association between Early-Onset Parkinson's Disease and Mutations in the<i>Parkin</i>Gene

Christoph B. Lücking, Alexandra Dürr, Vincenzo Bonifati et al. · New England Journal of Medicine · 2000 · 1.4K citations · Full text

Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

Giorgio Casari, Maurizio De Fusco, Sonia Ciarmatori et al. · Cell · 1998 · 824 citations · Full text

Mitochondrial Function, Oxphos Impairment, Genetics +10

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

N. Abbas, C.B. Lücking, Sylvain Ricard et al. · Human Molecular Genetics · 1999 · 531 citations

Early-onset parkinsonism associated with <i>PINK1</i> mutations

Vincenzo Bonifati, Christan F. Rohé, Guido J. Breedveld et al. · Neurology · 2005 · 335 citations

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

Luigia Atorino, Laura Silvestri, Mirko Koppen et al. · The Journal of Cell Biology · 2003 · 283 citations · Full text