• 1 Citations
  • 1 h-Index
20182019
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Fingerprint Dive into the research topics where Daisy Sproviero is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Aicardi Syndrome Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
RNA Engineering & Materials Science
Interferons Medicine & Life Sciences
Disease Progression Medicine & Life Sciences
Molecular Biology Medicine & Life Sciences
coding Social Sciences

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Research Output 2018 2019

  • 1 Citations
  • 1 h-Index
  • 5 Article
Amyotrophic Lateral Sclerosis
Disease Progression
Leukocytes
Biomarkers
Alzheimer Disease

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

Garau, J., Cavallera, V., Valente, M., Tonduti, D., Sproviero, D., Zucca, S., Battaglia, D., Battini, R., Bertini, E., Cappanera, S., Chiapparini, L., Crasà, C., Crichiutti, G., Dalla Giustina, E., D'Arrigo, S., De Giorgis, V., De Simone, M., Galli, J., La Piana, R., Messana, T. & 19 others, Moroni, I., Nardocci, N., Panteghini, C., Parazzini, C., Pichiecchio, A., Pini, A., Ricci, F., Saletti, V., Salvatici, E., Santorelli, F. M., Sartori, S., Tinelli, F., Uggetti, C., Veneselli, E., Zorzi, G., Garavaglia, B., Fazzi, E., Orcesi, S. & Cereda, C., May 26 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

Aicardi Syndrome
Interferons
Molecular Biology
Mutation
Genes

Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis

Bordoni, M., Pansarasa, O., Dell'Orco, M., Crippa, V., Gagliardi, S., Sproviero, D., Bernuzzi, S., Diamanti, L., Ceroni, M., Tedeschi, G., Poletti, A. & Cereda, C., May 22 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Oxidative Stress
DNA Damage
DNA
Ataxia Telangiectasia
Profiling
RNA
Blood
coding
Lateral
1 Citation (Scopus)

Encephalopathies with intracranial calcification in children: Clinical and genetic characterization

Tonduti, D., Panteghini, C., Pichiecchio, A., Decio, A., Carecchio, M., Reale, C., Moroni, I., Nardocci, N., Campistol, J., Garcia-Cazorla, A., Perez Duenas, B., Zorzi, G., Ardissone, A., Granata, T., Freri, E., Zibordi, F., Ragona, F., D'Arrigo, S., Saletti, V., Esposito, S. & 22 others, Pantaleoni, C., Riva, D., De Giorgis, V., Cereda, C., Valente, M. L., Sproviero, D., Poo Arguelles, M. P., Estupina, C. F., Sans Fito, A. M., Martorell Sampol, L., Del Mar O'Callaghan Gordo, M., Ortez Gonzalez, C. I., Gonzalez Alvarez, V., Garcia-Segarra, N., Fusco, C., Bertini, E., Diodato, D., Fazzi, E., Galli, J., Chiapparini, L., Garavaglia, B. & Orcesi, S., Aug 16 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 135.

Research output: Contribution to journalArticle

Brain Diseases
Genes
Exome
Phenotype
Inborn Genetic Diseases