Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Faustina Lalatta"'
Autor:
Maria Francesca Bedeschi, Mariarosaria Calvello, Leda Paganini, Lidia Pezzani, Marco Baccarin, Laura Fontana, Silvia M. Sirchia, Silvana Guerneri, Lorena Canazza, Ernesto Leva, Lorenzo Colombo, Faustina Lalatta, Fabio Mosca, Silvia Tabano, Monica Miozzo
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
Abstract Background Omphalocele is a congenital midline ventral body wall defect that can exist as isolated malformation or as part of a syndrome. It can be considered one of the major and most frequent clinical manifestation of Beckwith-Wiedemann Sy
Externí odkaz:
https://doaj.org/article/d6777ba42dcd4433ae219687367c081d
Autor:
Maria Elena Lunati, Maria Francesca Bedeschi, Veronica Resi, Valeria Grancini, Eva Palmieri, Simona Salera, Faustina Lalatta, Giuseppe Pugliese, Emanuela Orsi
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185371 (2017)
OBJECTIVE:The Williams-Beuren syndrome (WS) is associated with impaired glucose metabolism (IGM) early in adulthood. However, the pathophysiology of IGM remains poorly defined, due to the lack of longitudinal studies investigating the contribution of
Externí odkaz:
https://doaj.org/article/eb1392f927fc45fc80b58c4dcef6e2f4
Autor:
Angelo D'Ambrosio, Eleonora Agricola, Luisa Russo, Francesco Gesualdo, Elisabetta Pandolfi, Renata Bortolus, Carlo Castellani, Faustina Lalatta, Pierpaolo Mastroiacovo, Alberto Eugenio Tozzi
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0122551 (2015)
BACKGROUND:The risk of adverse pregnancy outcomes can be minimized through the adoption of healthy lifestyles before pregnancy by women of childbearing age. Initiatives for promotion of preconception health may be difficult to implement. Internet can
Externí odkaz:
https://doaj.org/article/a9a24c5055d64745b4b9bd61e07c24d3
Autor:
Vlasta Fesslova, Jelena Brankovic, Faustina Lalatta, Laura Villa, Valerio Meli, Luciane Piazza, Cristian Ricci
Publikováno v:
Journal of Pregnancy, Vol 2011 (2011)
Objectives. To evaluate the recurrence of congenital heart disease (CHD) in pregnant women with familial risk who had been referred for fetal echocardiography. Material and Methods. 1634 pregnancies from 1483 women with familial history of CHD in one
Externí odkaz:
https://doaj.org/article/b4200f5d08914e108a2264ebb72c9a2d
Autor:
Alessandra Provera, Paola Zanchi, Gaia Silibello, Francesca Dall’Ara, Claudia Rigamonti, Federico Monti, Paola Francesca Ajmone, Faustina Lalatta, Maria Antonella Costantino, Paola Giovanna Vizziello, Laura Zampini
Publikováno v:
First Language. 42:613-627
The neuropsychological profile associated with sex chromosome trisomies (SCT) is frequently characterised by delays or deficits in linguistic development. Although maternal input could have an important role in influencing and shaping the linguistic
Autor:
Paola Vizziello, Laura Zampini, Francesca Dall'Ara, Faustina Lalatta, Maria Antonella Costantino, Federico Monti, Claudia Rigamonti, Gaia Silibello, Paola Francesca Ajmone
Publikováno v:
Children's Health Care. 50:324-337
The study investigates the experience of the parents of 48 children who have prenatally diagnosed with Klinefelter syndrome [KS] using a specifically developed questionnaire. Fifty percent of the participants were satisfied with the disclosure proces
Autor:
Paola Zanchi, Laura Zampini, Paola Vizziello, Claudia Rigamonti, Francesca Dall'Ara, Federico Monti, Maria Antonella Costantino, Elena Capelli, Gaia Silibello, Paola Francesca Ajmone, Tiziana Burla, Faustina Lalatta
Publikováno v:
First Language. 41:200-217
Individuals with sex chromosome trisomies (SCTs) have an increased risk of language delays and impairments. However, there are only a few data relative to their language development in early childhood. The present study aimed to investigate the preve
Autor:
Claudia Rigamonti, Paola Vizziello, Francesca Dall'Ara, Faustina Lalatta, Maria Antonella Costantino, Laura Zampini, Camilla Ferrante, Paola Zanchi, Gaia Silibello
Publikováno v:
International Journal of Language & Communication Disorders. 55:724-733
Background: Although language difficulties are one of the most distinctive characteristics of the neuropsychological profile of children with sex chromosome trisomies (SCT), the analysis of the maternal input addressed to them is a neglected topic. A
Autor:
Francesca Dall'Ara, Gaia Silibello, Claudia Rigamonti, Paola Francesca Ajmone, Paola Vizziello, Laura Zampini, Federico Monti, Alessandra Lorini, Maria Antonella Costantino, Faustina Lalatta
OBJECTIVE: Children and adolescents with sex chromosome trisomies (SCTs) usually show a higher frequency of behavioral problems than typically developing (TD) children. However, little is known about the presence of behavioral issues in toddlers with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5f6c184a382ec7daf11fa048d57c9a
http://hdl.handle.net/10281/332571
http://hdl.handle.net/10281/332571
Autor:
Laura Zampini, Alessandra Lorini, Gaia Silibello, Paola Zanchi, Francesca Dall’Ara, Paola Francesca Ajmone, Federico Monti, Faustina Lalatta, Maria Antonella Costantino, Paola Giovanna Vizziello
Publikováno v:
International Journal of Environmental Research and Public Health, Vol 19, Iss 1831, p 1831 (2022)
International Journal of Environmental Research and Public Health; Volume 19; Issue 3; Pages: 1831
International Journal of Environmental Research and Public Health; Volume 19; Issue 3; Pages: 1831
Many individual factors, such as early communicative skills, could play a role in explaining later linguistic outcomes. The detection of predictive variables is fundamental to identifying early the children who need intervention. The present study fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a380040f9ae9c52b5afd063536fda5
http://hdl.handle.net/10281/352493
http://hdl.handle.net/10281/352493