A. Prelle

发表

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

N. Bresolin, G. Comi, G. Scarlato, 1994, Journal of the Neurological Sciences.

ENDOTHELIAL GROWTH FACTOR GENE TRANSFER USING ADENO-ASSOCIATED VIRAL VECTORS STIMULATES SKELETAL MUSCLE REGENERATION AND ENHANCES MUSCLE FUNCTION IN MDX MICE

E. Mercuri, E. Ricci, L. Morandi, 2006 .

Propranolol for familial cerebral cavernous malformation (Treat_CCM): study protocol for a randomized controlled pilot trial

V. Torri, S. Marino, R. Pallini, 2020, Trials.

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle

G. Scarlato, M. Moggio, M. Sciacco, 1996, Journal of the Neurological Sciences.

Sarcoglycan deficiency in a large Italian population of myopathic patients

G. Comi, G. Scarlato, M. Moggio, 1998, Acta Neuropathologica.

Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency

N. Bresolin, G. Comi, G. Scarlato, 2003, Acta Neuropathologica.

Skin‐derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection

A. Farini, Maria Cristina Tanzi, S. M. Gaini, 2007, Glia.

Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level

G. Comi, M. Zeviani, G. Scarlato, 1994, Acta Neuropathologica.

High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm

G. Bernardi, C. Angelini, C. Bruno, 2006, Neurological Sciences.