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C Doriguzzi

Showing results (51-60 of 55) with videos related to

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Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
European Neurology|January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalisC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of the Neurological Sciences|December 1, 1990
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trialN Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2007
Variable responses to rituximab treatment in neuromyelitis optica (Devic's disease)M Capobianco, S Malucchi, A di Sapio, et al.
Nature Genetics|September 1, 1993
Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermiaK A Quane, J M Healy, K E Keating, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
European Neurology|January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalisC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of the Neurological Sciences|December 1, 1990
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trialN Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2007
Variable responses to rituximab treatment in neuromyelitis optica (Devic's disease)M Capobianco, S Malucchi, A di Sapio, et al.
Nature Genetics|September 1, 1993
Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermiaK A Quane, J M Healy, K E Keating, et al.
Pageof 6