• 12845 Citations
  • 66 h-Index
1993 …2019
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Fingerprint Dive into the research topics where Valerio Carelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 15 Similar Profiles
Leber's Hereditary Optic Atrophy Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Mutation Medicine & Life Sciences
Autosomal Dominant Optic Atrophy Medicine & Life Sciences
Mitochondrial Diseases Medicine & Life Sciences
Optic Nerve Diseases Medicine & Life Sciences
Retinal Ganglion Cells Medicine & Life Sciences
Nerve Fibers Medicine & Life Sciences

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Research Output 1993 2019

Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-up

Parisi, V., Ziccardi, L., Sadun, F., De Negri, A. M., La Morgia, C., Barbano, L., Carelli, V. & Barboni, P., Jul 1 2019, In : Ophthalmology. 126, 7, p. 1033-1044 12 p.

Research output: Contribution to journalArticle

Open Access
Leber's Hereditary Optic Atrophy
Visual Pathways
Retinal Ganglion Cells
Visual Evoked Potentials
Analysis of Variance
1 Citation (Scopus)

Muscle pain in mitochondrial diseases: a picture from the Italian network

Filosto, M., Cotti Piccinelli, S., Lamperti, C., Mongini, T., Servidei, S., Musumeci, O., Tonin, P., Santorelli, F. M., Simoncini, C., Primiano, G., Vercelli, L., Rubegni, A., Galvagni, A., Moggio, M., Comi, G. P., Carelli, V., Toscano, A., Padovani, A., Siciliano, G. & Mancuso, M., Jan 1 2019, In : Journal of Neurology.

Research output: Contribution to journalReview article

Mitochondrial Diseases
Myalgia
Kearns-Sayre Syndrome
Mitochondrial DNA
Mutation

Muscle pain in mitochondrial diseases: a picture from the Italian network

Filosto, M., Cotti Piccinelli, S., Lamperti, C., Mongini, T., Servidei, S., Musumeci, O., Tonin, P., Santorelli, F. M., Simoncini, C., Primiano, G., Vercelli, L., Rubegni, A., Galvagni, A., Moggio, M., Comi, G. P., Carelli, V., Toscano, A., Padovani, A., Siciliano, G. & Mancuso, M., 2019, In : Journal of Neurology. 266, 4, p. 953-959 7 p.

Research output: Contribution to journalArticle

Novel mutations in DNA2 associated with myopathy and mtDNA instability

Ronchi, D., Liu, C., Caporali, L., Piga, D., Li, H., Tagliavini, F., Valentino, M. L., Ferrò, M. T., Bini, P., Zheng, L., Carelli, V., Shen, B. & Comi, G. P., 2019, In : Annals of Clinical and Translational Neurology. 6, 9, p. 1893-1899

Research output: Contribution to journalArticle

Open Access
Muscular Diseases
Mitochondrial DNA
Mutation
Mitochondrial Myopathies
Nuclear Proteins

Cerebral mitochondrial microangiopathy leads to leukoencephalopathy in mitochondrial neurogastrointestinal encephalopathy

Gramegna, L. L., Pisano, A., Testa, C., Manners, D. N., D'Angelo, R., Boschetti, E., Giancola, F., Pironi, L., Caporali, L., Capristo, M., Valentino, M. L., Plazzi, G., Casali, C., Dotti, M. T., Cenacchi, G., Hirano, M., Giordano, C., Parchi, P., Rinaldi, R., De Giorgio, R. & 3 others, Lodi, R., Carelli, V. & Tonon, C., Mar 1 2018, In : American Journal of Neuroradiology. 39, 3, p. 427-434 8 p.

Research output: Contribution to journalArticle

Cerebral Small Vessel Diseases
Leukoencephalopathies
Thymidine Phosphorylase
Brain
DNA Replication