Carlo Rinaldi

A candidate gene for autoimmune myasthenia gravis.

Insulinlike growth factor (IGF)-1 administration ameliorates disease manifestations in a mouse model of spinal and bulbar muscular atrophy.

Cowchock syndrome is associated with a mutation in apoptosis-inducing factor.

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.

Muscle matters in Kennedy's disease.

Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage.

Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat.

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.

Targeted Molecular Therapies for SBMA.

MiR-298 Counteracts Mutant Androgen Receptor Toxicity in Spinal and Bulbar Muscular Atrophy.

From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?

Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease.