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

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Klinefelter Syndrome Medicine & Life Sciences
Rare Diseases Medicine & Life Sciences
Parents Medicine & Life Sciences
Argininosuccinic Aciduria Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Medicine & Life Sciences
De Lange Syndrome Medicine & Life Sciences
Sex Chromosomes Medicine & Life Sciences

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Research Output 1984 2019

Klinefelter Syndrome in preschool children: the importance of an early multidisciplinary approach for patients and families

Rigamonti, C., Vizziello, P., Monti, F., Dall'ara, F., Ajmone, P. F., Giavoli, C., Silibello, G. & Lalatta, F., Oct 1 2019, In : Minerva Pediatrica. 71, 5, p. 395-403 9 p.

Research output: Contribution to journalArticle

Klinefelter Syndrome
Preschool Children

A de novo C19orf12 heterozygous mutation in a patient with MPAN

Monfrini, E., Melzi, V., Buongarzone, G., Franco, G., Ronchi, D., Dilena, R., Scola, E., Vizziello, P., Bordoni, A., Bresolin, N., Comi, G. P., Corti, S. & Di Fonzo, A., 2018, In : Parkinsonism and Related Disorders. 48, p. 109-111

Research output: Contribution to journalArticle

Early communicative skills of children with Klinefelter syndrome

Zampini, L., Burla, T., Silibello, G., Dall’Ara, F., Rigamonti, C., Lalatta, F. & Vizziello, P., 2018, In : Clinical Linguistics and Phonetics. 32, 7, p. 577-586 10 p.

Research output: Contribution to journalArticle

Klinefelter Syndrome

Vocal and gestural productions of 24-month-old children with sex chromosome trisomies

Zampini, L., Draghi, L., Silibello, G., Dall'Ara, F., Rigamonti, C., Suttora, C., Zanchi, P., Salerni, N., Lalatta, F. & Vizziello, P., Jan 1 2018, In : International Journal of Language and Communication Disorders. 53, 1, p. 171-181 11 p.

Research output: Contribution to journalArticle

Sex Chromosomes
Klinefelter Syndrome

Daily life changes and adaptations investigated in 154 families with a child suffering from a rare disability at a public centre for rare diseases in Northern Italy

Silibello, G., Vizziello, P., Gallucci, M., Selicorni, A., Milani, D., Ajmone, P. F., Rigamonti, C., De Stefano, S., Bedeschi, M. F. & Lalatta, F., Aug 31 2016, In : Italian Journal of Pediatrics. 42, 1, 76.

Research output: Contribution to journalArticle

Rare Diseases
Family Relations
Disabled Children
Delivery of Health Care