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

  • 17 Similar Profiles
Prenatal Diagnosis Medicine & Life Sciences
Mutation Medicine & Life Sciences
Pregnancy Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Williams Syndrome Medicine & Life Sciences
Genes Medicine & Life Sciences
Karyotype Medicine & Life Sciences
Parents Medicine & Life Sciences

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Research Output 1981 2019

  • 1925 Citations
  • 21 h-Index
  • 126 Article
  • 1 Chapter
  • 1 Letter
Williams Syndrome
Bone Density
Phosphorus
Minerals
Bone and Bones

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
Parents
Emotions
Language

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D’Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M. & Tabano, S., 2018, In : Epigenetics. 13, 9, p. 897-909 13 p.

Research output: Contribution to journalArticle

Chromosomes
Silver
Methylation
Silver-Russell Syndrome
Genomic Imprinting

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D'Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M. & Tabano, S., 2018, In : Epigenetics. 13, 9, p. 897-909 13 p.

Research output: Contribution to journalArticle

Chromosomes
Silver
Methylation
Silver-Russell Syndrome
Genomic Imprinting