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

Medicine & Life Sciences

Mutation
Genes
Duchenne Muscular Dystrophy
Mitochondrial DNA
Muscles
Amyotrophic Lateral Sclerosis
Dystrophin
Motor Neurons
Phenotype
Muscular Diseases
Mitochondrial Diseases
Chronic Progressive External Ophthalmoplegia
Skeletal Muscle
Spinal Muscular Atrophy
Muscular Dystrophies
Population
Neural Stem Cells
Glycogen Storage Disease Type II
Limb-Girdle Muscular Dystrophies
Exons
coenzyme Q10
Biopsy
Therapeutics
Induced Pluripotent Stem Cells
Glycogen Storage Disease Type III
Proteins
Mitochondrial Encephalomyopathies
Stroke
Mitochondrial Myopathies
Genome-Wide Association Study
Motor Neuron Disease
Neurodegenerative Diseases
Haplotypes
Introns
Italy
Genotype
Muscle Weakness
Myotonia Congenita
Electron Transport
Disease Progression
Brain
Cytochrome-c Oxidase Deficiency
Dystroglycans
Vascular Endothelial Growth Factor A
Registries
Genome
Age of Onset
Stem Cells
MELAS Syndrome
Leigh Disease