Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

Por Yoneda, M, Chomyn, A, Martinuzzi, A, Hurko, O, Attardi, G
Publicado em 1992

Expanding cerebral cysts (lacunae): a treatable cause of progressive midbrain syndrome

Por Longatti, P, Fiorindi, A, Carteri, A, Caroli, F, Martinuzzi, A
Publicado em 2003

Chronic therapy for McArdle disease: the randomized trial with ACE inhibitor

Por Martinuzzi, A, Liava, A, Trevisi, E, Antoniazzi, L, Frare, M
Publicado em 2007

Coiling and neuroendoscopy: a new perspective in the treatment of intraventricular haemorrhages due to bleeding aneurysms

Por Longatti, P, Fiorindi, A, Paola, F Di, Curtolo, S, Basaldella, L, Martinuzzi, A
Publicado em 2006

Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.

Por Martinuzzi, A, Vergani, L, Carrozzo, R, Fanin, M, Bartoloni, L, Angelini, C, Askanas, V, Engel, W K
Publicado em 1993

Psychological Profile in Children and Adolescents with Severe Course Juvenile Idiopathic Arthritis

Por Russo, Emanuela, Trevisi, E., Zulian, F., Battaglia, M. A., Viel, D., Facchin, D., Chiusso, A., Martinuzzi, A.
Publicado em 2012

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream...

Por Chomyn, A, Martinuzzi, A, Yoneda, M, Daga, A, Hurko, O, Johns, D, Lai, S T, Nonaka, I, Angelini, C, Attardi, G
Publicado em 1992

Children in Vegetative State and Minimally Conscious State: Patients' Condition and Caregivers' Burden

Por Giovannetti, A. M., Pagani, M., Sattin, D., Covelli, V., Raggi, A., Strazzer, S., Castelli, E., Trabacca, A., Martinuzzi, A., Leonardi, M.
Publicado em 2012

Training on the International Classification of Functioning, Disability and Health (ICF): the ICF–DIN Basic and the ICF–DIN Advanced Course developed by the Disability Italian Netw...

Por Leonardi*, M., Bickenbach, J., Raggi, A., Sala, M., Guzzon, P., Valsecchi, M. R., Fusaro, G., Russo, E., Francescutti, C., Nocentini, U., Martinuzzi, A.
Publicado em 2005

A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.

Por Bruno, C, Martinuzzi, A, Tang, Y, Andreu, A L, Pallotti, F, Bonilla, E, Shanske, S, Fu, J, Sue, C M, Angelini, C, DiMauro, S, Manfredi, G
Publicado em 1999