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

Medicine & Life Sciences

Mutation
Muscles
Inclusion Body Myositis
Glycogen Storage Disease Type III
Skeletal Muscle
Congenital Structural Myopathies
Genes
Mitochondrial DNA
Biopsy
Cytochrome-c Oxidase Deficiency
Glycogen Storage Disease Type IV
Charcot-Marie-Tooth Disease
RNA, Transfer, Asn
Hepatomegaly
Genetic Association Studies
Endosomal Sorting Complexes Required for Transport
Nemaline Myopathies
Knockout Mice
Myelin P0 Protein
Glycogen
Spermatids
Protein-Restricted Diet
Glycogen Storage Disease Type II
Churg-Strauss Syndrome
Anaerobic Threshold
Enzyme Replacement Therapy
Spinocerebellar Ataxias
Spinal Muscular Atrophy
Microtubules
Ophthalmoplegia
Acrosome
Autophagy
Peripheral Nerves
Duchenne Muscular Dystrophy
Muscle Development
Purkinje Cells
Germ Cells
Huntington Disease
Nuclear Envelope
Organelle Biogenesis
Exercise
Ubiquitin
Urinary Bladder Neoplasms
Vacuoles
Phenotype
Liver
Muscular Diseases
Melanoma
Lactic Acid
Exome