M. Rimoldi

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

Massimo Zeviani, Cinzia Gellera, Carlo Antozzi et al. · The Lancet · 1991 · 383 citations

Mitochondrial Myopathy, Mendelian Disorder, Genetic Disorder +8

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

Caterina Mariotti, Cinzia Gellera, M. Rimoldi et al. · Neurological Sciences · 2004 · 154 citations

Mendelian Disorder, Genetic Disorder, Inherited Metabolic Disease +8

Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients

Stefano DiDonato, Massimo Zeviani, P. Giovannini et al. · Neurology · 1993 · 98 citations

Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes

Cinzia Gellera, Graziella Uziel, M. Rimoldi et al. · Neurology · 1990 · 96 citations

Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiency

Stefano Di Donato, M. Rimoldi, Barbara Garavaglia et al. · Clinica Chimica Acta · 1984 · 89 citations

Urology, Physiology, Propionylcarnitine Excretion +4