Lista de obras -

3D Neuronal Mitochondrial Morphology in Axons, Dendrites, and Somata of the Aging Mouse Hippocampus

artículo científico publicado en 2021

A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.

artículo científico publicado en 2015

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.

artículo científico publicado en 2016

Diagnosis and Treatment of Mitochondrial Myopathies

artículo científico publicado en 2018

Distinctive Features of Orbital Adipose Tissue (OAT) in Graves' Orbitopathy

scientific article published on 30 November 2020

Dysferlin mutations and mitochondrial dysfunction

artículo científico publicado en 2016

Expanding Our Understanding of mtDNA Deletions.

artículo científico publicado en 2016

Formation of mitochondrial-derived vesicles is an active and physiologically relevant mitochondrial quality control process in the cardiac system.

artículo científico publicado en 2016

Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues

artículo científico publicado en 2019

Mitochondrial Nanotunnels

artículo científico publicado en 2017

Mitochondrial dysfunction in myofibrillar myopathy.

artículo científico publicado en 2016

Mitochondrial morphology and function: two for the price of one!

scientific article published on 11 April 2020

Mosaic dysfunction of mitophagy in mitochondrial muscle disease

artículo científico publicado en 2022

Multilevel heterogeneity of mitochondrial respiratory chain deficiency

artículo científico publicado en 2018

Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

artículo científico publicado en 2019

Subcellular origin of mitochondrial DNA deletions in human skeletal muscle

The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy.

scientific article published on 10 August 2016

Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level

artículo científico publicado en 2019

Lista de obras de

3D Neuronal Mitochondrial Morphology in Axons, Dendrites, and Somata of the Aging Mouse Hippocampus

A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.

Diagnosis and Treatment of Mitochondrial Myopathies

Distinctive Features of Orbital Adipose Tissue (OAT) in Graves' Orbitopathy

Dysferlin mutations and mitochondrial dysfunction

Expanding Our Understanding of mtDNA Deletions.

Formation of mitochondrial-derived vesicles is an active and physiologically relevant mitochondrial quality control process in the cardiac system.

Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues

Mitochondrial Nanotunnels

Mitochondrial dysfunction in myofibrillar myopathy.

Mitochondrial morphology and function: two for the price of one!

Mosaic dysfunction of mitophagy in mitochondrial muscle disease

Multilevel heterogeneity of mitochondrial respiratory chain deficiency

Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

Subcellular origin of mitochondrial DNA deletions in human skeletal muscle

The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy.

Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level