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

Medicine & Life Sciences

MELAS Syndrome
Limb-Girdle Muscular Dystrophies
Karyopherins
MicroRNAs
Hearing Loss
Muscular Diseases
Temporal Bone
Muscles
Phenotype
Extremities
Nuclear Family
Mutation
Muscular Dystrophies
Brain
Mothers
Magnetic Resonance Imaging
Somatotypes
Inborn Genetic Diseases
Spiral Ganglion
Atrophy
Proteins
Cochlea
Glycogen Storage Disease Type VII
Myotonia Congenita
Glycogen Storage Disease Type IV
Exome
Genetic Techniques
Genes
Lafora Disease
Muscular Atrophy
Muscle Weakness
Amylopectin
DNA Sequence Analysis
Genetic Therapy
Striated Muscle
Stria Vascularis
Hypertrophic Cardiomyopathy
Auditory Pathways
Lower Extremity
Nervous System Diseases
Glycogen
Rehabilitation
Central Nervous System
Polysaccharides
Smooth Muscle
Inner Ear
Molecular Biology
Biopsy
Skeletal Muscle
Drug Therapy