Lista de obras -

Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS.

artículo científico publicado en 2016

Alzheimer's pathogenesis and its link to the mitochondrion

artículo científico publicado en 2015

Common Genetic Conditions of Ischemic Stroke to Keep in Mind.

artículo científico publicado en 2014

Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study.

artículo científico publicado en 2016

Disruption of sleep-wake continuum in myotonic dystrophy type 1: Beyond conventional sleep staging

artículo científico publicado en 2018

Drugs and mitochondrial diseases: 40 queries and answers.

artículo científico

Effects of aerobic training on exercise-related oxidative stress in mitochondrial myopathies.

artículo científico publicado en 2012

Fabry disease with atypical neurological presentation: report of a case

scientific article published on 01 November 2012

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany

artículo científico publicado en 2014

Metabolic myopathies: functional evaluation by different exercise testing approaches.

artículo científico publicado en 2011

Mitochondrial DNA haplogroups may influence Fabry disease phenotype

Muscle pain in mitochondrial diseases: a picture from the Italian network

article

Oxidative stress and APO E polymorphisms in Alzheimer's disease and in mild cognitive impairment.

artículo científico publicado en 2013

Physical exercise and oxidative stress in muscular dystrophies: is there a good balance?

artículo científico publicado en 2017

Relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1

artículo científico publicado en 2016

Tetracycline treatment in patients with progressive external ophthalmoplegia

artículo científico publicado en 2011

The proposal of a clinical protocol to assess central and peripheral fatigue in myotonic dystrophy type 1.

artículo científico

Vascular factors and mitochondrial dysfunction: a central role in the pathogenesis of Alzheimer's disease.

artículo científico

Lista de obras de

Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS.

Alzheimer's pathogenesis and its link to the mitochondrion

Common Genetic Conditions of Ischemic Stroke to Keep in Mind.

Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study.

Disruption of sleep-wake continuum in myotonic dystrophy type 1: Beyond conventional sleep staging

Drugs and mitochondrial diseases: 40 queries and answers.

Effects of aerobic training on exercise-related oxidative stress in mitochondrial myopathies.

Fabry disease with atypical neurological presentation: report of a case

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany

Metabolic myopathies: functional evaluation by different exercise testing approaches.

Mitochondrial DNA haplogroups may influence Fabry disease phenotype

Muscle pain in mitochondrial diseases: a picture from the Italian network

Oxidative stress and APO E polymorphisms in Alzheimer's disease and in mild cognitive impairment.

Physical exercise and oxidative stress in muscular dystrophies: is there a good balance?

Relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1

Tetracycline treatment in patients with progressive external ophthalmoplegia

The proposal of a clinical protocol to assess central and peripheral fatigue in myotonic dystrophy type 1.

Vascular factors and mitochondrial dysfunction: a central role in the pathogenesis of Alzheimer's disease.