Publications by authors named "Massimo Bado"

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Phenotypic characterization of hypomyelination and congenital cataract.
Roberta Biancheri, Federico Zara, Claudio Bruno, Andrea Rossi, Laura Bordo, Massimo Bado

Ann Neurol· August 2007

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Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene.
Claudio Bruno, Filippo M Santorelli, Stefania Assereto, Emmanuel Tonoli, Alessandra Tessa, Massimo Bado

Muscle Nerve· October 2003

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Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.
Claudio Bruno, Oliviero Sacco, Filippo M Santorelli, Stefania Assereto, Emmanuel Tonoli, Massimo Bado

J Child Neurol· April 2003

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Altered aquaporin-4 expression in human muscular dystrophies: a common feature?
Antonio Frigeri, Grazia Paola Nicchia, Silvia Repetto, Massimo Bado, Carlo Minetti

FASEB J· July 2002

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A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
Claudio Bruno, Roberta Biancheri, Barbara Garavaglia, Claudia Biedi, Andrea Rossi, Massimo Bado

J Child Neurol· March 2002

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Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency.
Carlo Minetti, Massimo Bado, Paolo Broda, Federica Sotgia, Claudio Bruno

Am J Pathol· January 2002

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