• 478 Citations
  • 15 h-Index
20012019
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Fingerprint Dive into the research topics where Francesca Tinelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Aptitude Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences
Periventricular Leukomalacia Medicine & Life Sciences
Brain Medicine & Life Sciences
Visual Fields Medicine & Life Sciences
Down Syndrome Medicine & Life Sciences
Cerebral Palsy Medicine & Life Sciences
Vision Disorders Medicine & Life Sciences

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Research Output 2001 2019

  • 478 Citations
  • 15 h-Index
  • 48 Article
  • 1 Chapter
  • 1 Short survey

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

Visual assessment in Down Syndrome: The relevance of early visual functions

Purpura, G., Bacci, G. M., Bargagna, S., Cioni, G., Caputo, R. & Tinelli, F., Apr 2019, In : Early Human Development. 131, p. 21-28 8 p.

Research output: Contribution to journalArticle

Down Syndrome
Visual Acuity
Refractive Errors
Fundus Oculi
Hyperopia
Cerebral Palsy
Aptitude
Confidence Intervals
Reproducibility of Results
Research
Periventricular Leukomalacia
Cerebral Palsy
Disabled Children
Clinical Protocols
Automatic Data Processing

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

D'Amore, A., Tessa, A., Casali, C., Dotti, M. T., Filla, A., Silvestri, G., Antenora, A., Astrea, G., Barghigiani, M., Battini, R., Battisti, C., Bruno, I., Cereda, C., Dato, C., Di Iorio, G., Donadio, V., Felicori, M., Fini, N., Fiorillo, C., Gallone, S. & 33 others, Gemignani, F., Gigli, G. L., Graziano, C., Guerrini, R., Gurrieri, F., Kariminejad, A., Lieto, M., Marques LourenḈo, C., Malandrini, A., Mandich, P., Marcotulli, C., Mari, F., Massacesi, L., Melone, M. A. B., Mignarri, A., Milone, R., Musumeci, O., Pegoraro, E., Perna, A., Petrucci, A., Pini, A., Pochiero, F., Pons, M. R., Ricca, I., Rossi, S., Seri, M., Stanzial, F., Tinelli, F., Toscano, A., Valente, M., Federico, A., Rubegni, A. & Santorelli, F. M., 2018, In : Frontiers in Neurology. 9, p. 981

Research output: Contribution to journalArticle

Hereditary Spastic Paraplegia
Cross-Sectional Studies
Genes
Pyramidal Tracts
Mutation