F. Mazzucchelli

发表

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication.

N. Bresolin, G. Scarlato, G. Attardi, 1999, Science.

The Neurologist in the Emergency Room: Prospective Study of the Neurological Emergency Group in Lombardia

C. Piazza, C. Scaccabarozzi, I. Santilli, 2019, J. of Health Science.

Cognitive impairment in Duchenne muscular dystrophy

N. Bresolin, D. Perani, F. Grassi, 1994, Neuromuscular Disorders.

Development of Dopaminergic Neurons in the Human Mesencephalon and in Vitro Effects of Basic Fibroblast Growth Factor Treatment

G. Pardi, G. Scarlato, V. Silani, 1994, Experimental Neurology.

Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells*

N. Bresolin, G. Scarlato, G. Attardi, 1996, The Journal of Biological Chemistry.

Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes

Davide Pareyson, Caterina Mariotti, Antonella Antonelli, 1999, Journal of Neurology.

In vivo and in vitro Development of Human Mesencephalic Dopaminergic Neurons

G. Pardi, G. Scarlato, V. Silani, 1992, Journal of Neural Transplantation & Plasticity.

Marked aging‐related decline in efficiency of oxidative phosphorylation in human skin fibroblasts

N. Bresolin, S. Papa, G. Attardi, 2003, The FASEB Journal.

Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 gene

S. di Donato, B. Castellotti, M. Pandolfo, 1997, Neurology.