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

  • 34 Similar Profiles
Dystonia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Movement Disorders Medicine & Life Sciences
Pantothenate Kinase-Associated Neurodegeneration Medicine & Life Sciences
Dystonic Disorders Medicine & Life Sciences
Neuroaxonal Dystrophies Medicine & Life Sciences
Genes Medicine & Life Sciences
Chorea Medicine & Life Sciences

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Research Output 1995 2019

Corrigendum to “Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum” [Brain Dev. 41 (2019) 250–256] (Brain and Development (2019) 41(3) (250–256), (S0387760418304959), (10.1016/j.braindev.2018.10.001))

Iodice, A., Carecchio, M., Zorzi, G., Garavaglia, B., Spagnoli, C., Salerno, G. G., Frattini, D., Mencacci, N. E., Invernizzi, F., Veneziano, L., Mantuano, E., Angriman, M. & Fusco, C., Jan 1 2019, In : Brain and Development.

Research output: Contribution to journalComment/debate

Open Access
Restless Legs Syndrome
Chorea
Brain Diseases
Mutation
Brain

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

Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications

Tonduti, D., Izzo, G., D'Arrigo, S., Riva, D., Moroni, I., Zorzi, G., Cavallera, V., Pichiecchio, A., Uggetti, C., Veggiotti, P., Orcesi, S., Chiapparini, L. & Parazzini, C., Feb 25 2019, In : Molecular Genetics and Metabolism. 126, 4, p. 489-94 6 p.

Research output: Contribution to journalArticle

Aicardi Syndrome
Magnetic resonance imaging
Monitoring
Chemical activation
Leukoencephalopathies
8 Citations (Scopus)

ATP1A3-related disorders: An update

Carecchio, M., Zorzi, G., Ragona, F., Zibordi, F. & Nardocci, N., Mar 1 2018, In : European Journal of Paediatric Neurology. 22, 2, p. 257-263 7 p.

Research output: Contribution to journalReview article

Dystonic Disorders
Mutation
CAPOS syndrome
Dystonia 12
Alternating hemiplegia of childhood
1 Citation (Scopus)

Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?

Invernizzi, F., Zorzi, G., Legati, A., Coppola, G., D'Adamo, P., Nardocci, N., Garavaglia, B. & Ghezzi, D., Oct 1 2018, In : European Journal of Medical Genetics. 61, 10, p. 581-584 4 p.

Research output: Contribution to journalArticle

Chorea
Haploinsufficiency
Hypothyroidism
Nervous System Diseases
Point Mutation