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

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

  • 7 Similar Profiles
Neurofibromatosis 1 Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Mutation Medicine & Life Sciences
Optic Nerve Glioma Medicine & Life Sciences
Pediatrics Medicine & Life Sciences
Arnold-Chiari Malformation Medicine & Life Sciences
Neurofibromatosis 1 Genes Medicine & Life Sciences
Intelligence Medicine & Life Sciences

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

Research Output 1996 2019

Brain tumors in NF1 children: Influence on neurocognitive and behavioral outcome

Taddei, M., Erbetta, A., Esposito, S., Saletti, V., Bulgheroni, S. & Riva, D., Nov 2019, In : Cancers. 11, 11, 1772.

Research output: Contribution to journalArticle

Open Access
Neurofibromatosis 1
Brain Neoplasms
Optic Nerve Glioma
Central Nervous System Neoplasms
Aptitude
Craniosynostoses
Decompression
Sutures
Syringomyelia
Papilledema

Chiari I malformation in defined genetic syndromes in children: are there common pathways?

Saletti, V., Viganò, I., Melloni, G., Pantaleoni, C., Vetrano, I. G. & Valentini, L. G., Oct 1 2019, In : Child's Nervous System. 35, 10, p. 1727-1739 13 p.

Research output: Contribution to journalArticle

Arnold-Chiari Malformation
Craniosynostoses
Phosphatidylinositol 3-Kinases
Nervous System Malformations
Inborn Genetic Diseases

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

Koczkowska, M., Callens, T., Chen, Y., Gomes, A., Hicks, A. D., Sharp, A., Johns, E., Uhas, K. A., Armstrong, L., Bosanko, K. A., Babovic-Vuksanovic, D., Baker, L., Basel, D. G., Bengala, M., Bennett, J. T., Chambers, C., Clarkson, L. K., Clementi, M., Cortés, F. M., Cunningham, M. & 88 others, D'Agostino, M. D., Delatycki, M. B., Digilio, M. C., Dosa, L., Esposito, S., Fox, S., Freckmann, M. L., Fauth, C., Giugliano, T., Giustini, S., Goetsch, A., Goldberg, Y., Greenwood, R. S., Griffis, C., Gripp, K. W., Gupta, P., Haan, E., Hachen, R. K., Haygarth, T. L., Hernández-Chico, C., Hodge, K., Hopkin, R. J., Hudgins, L., Janssens, S., Keller, K., Kelly-Mancuso, G., Kochhar, A., Korf, B. R., Lewis, A. M., Liebelt, J., Lichty, A., Listernick, R. H., Lyons, M. J., Maystadt, I., Martinez Ojeda, M., McDougall, C., McGregor, L. K., Melis, D., Mendelsohn, N., Nowaczyk, M. J. M., Ortenberg, J., Panzer, K., Pappas, J. G., Pierpont, M. E., Piluso, G., Pivnick, E. K., Pinna, V., Pond, D. A., Powell, C. M., Rogers, C., Ruhrman Shahar, N., Rutledge, S. L., Saletti, V., Sandaradura, S. A., Santoro, C., Schatz, U. A., Schreiber, A., Scott, D. A., Sellars, E. A., Sheffer, R., Siqveland, E., Slopis, J. M., Smith, R., Spalice, A., Stockton, D. W., Streff, H., Theos, A., Tomlinson, G. E., Tran, G., Trapane, P. L., Trevisson, E., Ullrich, N. J., Van den Ende, J., Schrier Vergano, S. A., Wallace, S. E., Wangler, M. F., Weaver, D. D., Yohay, K. H., Zackai, E., Zonana, J., Zurcher, V., Claes, K. B. M., Eoli, M., Martin, Y., Wimmer, K., De Luca, A., Legius, E. & Messiaen, L. M., Jan 1 2019, (Accepted/In press) In : Human Mutation.

Research output: Contribution to journalArticle

Open Access
Neurofibroma
Neurofibromatosis 1
Plexiform Neurofibroma
Optic Nerve Glioma
Cardiovascular Abnormalities

Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience

Ciaccio, C., Saletti, V., D'Arrigo, S., Esposito, S., Alfei, E., Moroni, I., Tonduti, D., Chiapparini, L., Pantaleoni, C. & Milani, D., 2019, In : European Journal of Medical Genetics. 62, 12, 103596.

Research output: Contribution to journalArticle

Pediatrics
Mutation
Megalencephaly
Vascular Malformations
Brain