If you made any changes in Pure these will be visible here soon.

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.

  • 22 Similar Profiles
MicroRNAs Medicine & Life Sciences
Limb-Girdle Muscular Dystrophies Medicine & Life Sciences
Glycogen Storage Disease Type IIb Medicine & Life Sciences
Phenotype Medicine & Life Sciences
MELAS Syndrome Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Muscles Medicine & Life Sciences
Duchenne Muscular Dystrophy Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2018 2019

A new family with transportinopathy: increased clinical heterogeneity

Angelini, C., Marozzo, R., Pinzan, E., Pegoraro, V., Molnar, M. J., Torella, A. & Nigro, V., 2019, In : Therapeutic Advances in Neurological Disorders. 12, p. 1756286419850433

Research output: Contribution to journalArticle

Karyopherins
Nuclear Family
Muscles
Mothers
Magnetic Resonance Imaging
Duchenne Muscular Dystrophy
Dystrophin
Cardiomyopathies
Walking
Therapeutics

MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathy

Pegoraro, V., Missaglia, S., Marozzo, R., Tavian, D. & Angelini, C., Jan 1 2019, (Accepted/In press) In : Muscle and Nerve.

Research output: Contribution to journalArticle

Open Access
MicroRNAs
Siblings
Biomarkers
Phenotype
Liver

Review: Danon disease: Review of natural history and recent advances

Cenacchi, G., Papa, V., Pegoraro, V., Marozzo, R., Fanin, M. & Angelini, C., Jan 1 2019, (Accepted/In press) In : Neuropathology and Applied Neurobiology.

Research output: Contribution to journalReview article

Glycogen Storage Disease Type IIb
Natural History
Lysosomes
Lysosome-Associated Membrane Glycoproteins
X-Linked Genes

Update on polyglucosan storage diseases

Cenacchi, G., Papa, V., Costa, R., Pegoraro, V., Marozzo, R., Fanin, M. & Angelini, C., Jan 1 2019, In : Virchows Archiv.

Research output: Contribution to journalReview article

Somatotypes
Inborn Genetic Diseases
Muscular Diseases
Glycogen Storage Disease Type VII
Glycogen Storage Disease Type IV