Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Antonia Squarcella"'
Autor:
F. Colloridi, F. Rech, S. Grisolia, Valentina D'Ambrosio, R. La Torre, Camilla Aliberti, Eleonora Marcoccia, S. Gatto, Antonia Squarcella, Antonella Giancotti
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology. 45:334-338
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36672892d8ad89c3a8d6c717245e754a
https://doi.org/10.12891/ceog4059.2018
https://doi.org/10.12891/ceog4059.2018
Autor:
Chiara Boccherini, Valentina D'Ambrosio, Antonella Giancotti, Flaminia Vena, Daniele Di Mascio, Antonia Squarcella, Roberto Brunelli, Sara Corno, Cristina Pajno, Maria Grazia Piccioni, Antonio Pizzuti
The aim of this study was to evaluate obstetrical and perinatal outcomes in fetuses with short femur length diagnosed before or after 24 weeks of gestation.This was a prospective cohort study on singleton pregnancies with a diagnosis of fetal femur5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc0cc07dcac2e74d54db1f78f66ac1f
http://hdl.handle.net/11573/1442909
http://hdl.handle.net/11573/1442909
Autor:
Sara Corno, Cristina Pajno, Antonio Pizzuti, Flaminia Vena, Roberto Brunelli, Antonia Squarcella, Maria G Piccioni, Daniele Di Mascio, Valentina D'Ambrosio, Pierluigi Benedetti Panici, Antonella Giancotti
Publikováno v:
Minerva Ginecologica. 71
Non-invasive prenatal testing (NIPT) has revolutionized the approach to prenatal diagnosis and, to date, it is the most superior screening method for the common autosomal aneuploidies, mostly trisomy 21. This screening is having a significant populat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b40cfff3e6129d92d4be44e07c27dd5
https://doi.org/10.23736/s0026-4784.18.04306-x
https://doi.org/10.23736/s0026-4784.18.04306-x
Autor:
G. Pasquali, Angela De Filippis, Antonella Giancotti, Valentina D'Ambrosio, Antonio Pizzuti, Eleonora Marcoccia, Aliberti Camilla, Antonia Squarcella, Renato Torre, Silvia Gatto
Publikováno v:
Journal of Clinical Ultrasound. 44:252-259
Proximal focal femoral deficiency (PFFD) is a rare musculoskeletal malformation that occurs in 0.11-0.2 per 10,000 live births. This congenital anomaly involves the pelvis and proximal femur with widely variable manifestations, from mild femoral shor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34d1d48c5f0dad1dc0cd7543c3cec11d
https://doi.org/10.1002/jcu.22306
https://doi.org/10.1002/jcu.22306
Autor:
Antonia Squarcella, Camilla Aliberti, Lucia Manganaro, Enrica Marchionni, Antonio Pizzuti, Antonella Giancotti, Valentina D'Ambrosio, Renato Torre
Pfeiffer syndrome (PS) is an autosomal dominant disorder caused by mutations in FGFR1 and FGFR2 genes. Given its wide range of clinical expression and severity, early prenatal diagnosis is difficult and genetic counseling is desirable. We report a li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d66a6c67f4221e273e10ec7da835ef29
http://hdl.handle.net/11573/907214
http://hdl.handle.net/11573/907214
Autor:
Valentina, D'Ambrosio, Gaia, Pasquali, Antonia, Squarcella, Eleonora, Marcoccia, Angela, De Filippis, Silvia, Gatto, Aliberti, Camilla, Antonio, Pizzuti, Renato, La Torre, Antonella, Giancotti
Proximal focal femoral deficiency (PFFD) is a rare musculoskeletal malformation that occurs in 0.11-0.2 per 10,000 live births. This congenital anomaly involves the pelvis and proximal femur with widely variable manifestations, from mild femoral shor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6168b5596d09c887dbd75e78cc6b90a0
http://hdl.handle.net/11573/856698
http://hdl.handle.net/11573/856698