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

Medicine & Life Sciences

Mutation
Mitochondrial Diseases
Phenotype
Leukoencephalopathies
Mitochondrial DNA
Genes
Peripheral Nervous System Diseases
Brain Diseases
Muscles
Exome
Lactic Acidosis
Electron Transport
Polyneuropathies
Dynamin I
Molecular Biology
Vitamin B 12
Cytochrome-c Oxidase Deficiency
Mitochondria
Muscular Diseases
Fibroblasts
Sideroblastic Anemia
Apoptosis Inducing Factor
Cell Nucleus Division
Mitochondrial Proteins
Optic Atrophy
Glycogen Storage Disease Type II
Amino Acyl-tRNA Synthetases
Cardiomyopathies
Age of Onset
Motor Neuron Disease
Mitochondrial Genome
Mitochondrial Encephalomyopathies
Biopsy
Leigh Disease
Liver Transplantation
Registries
Flavoproteins
Electron Transport Complex III
Muscle Hypotonia
Brain
Riboflavin Deficiency
Proteins
Signs and Symptoms
Hereditary Spastic Paraplegia
Chronic Progressive External Ophthalmoplegia
MELAS Syndrome
Deafness
Therapeutics
Acyl-CoA Dehydrogenase
Mitochondrial Myopathies