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Fingerprint Dive into the research topics where Rosalba Carrozzo is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Mutation
Mitochondrial DNA
Mitochondrial Diseases
Muscles
Genes
Phenotype
Electron Transport
Leigh Disease
Fibroblasts
Adenosine Triphosphate
Cytochrome-c Oxidase Deficiency
Leukoencephalopathies
Lactic Acidosis
Biopsy
Hypertrophic Cardiomyopathy
Mitochondria
Oxidative Phosphorylation
Proteins
Transfer RNA
Mitochondrial Proteins
Enzymes
Deafness
Carnitine
Riboflavin
Mitochondrial Encephalomyopathies
Friedreich Ataxia
Oxidative Stress
Mitochondrial Myopathies
coenzyme Q10
Chronic Progressive External Ophthalmoplegia
Glutathione
Skeletal Muscle
Exome
Brain Diseases
Dystonia
Electron Transport Complex IV
Mitochondrial Genes
Dynamin I
Oxidoreductases
Neurodegenerative Diseases
Sideroblastic Anemia
Neuronal Ceroid-Lipofuscinoses
Leber's Hereditary Optic Atrophy
Escherichia coli
Apoptosis Inducing Factor
Kearns-Sayre Syndrome
Muscular Diseases
Biomarkers
Chondroitin Sulfate Proteoglycans
Optic Atrophy

Chemical Compounds

Mitochondrial DNA
Fibroblasts
Mitochondria
Adenosine Triphosphate
Glutathione
Ceroid
Cells
Oxidative stress
coenzyme Q10
Genes