Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Giovanna Scassellati Sforzolini"'
Autor:
Daniela Valeriani, Federica Brosio, Pascale Riu, Vittorio Unfer, Mizar Paragona, Patrizia Logoteta, Giovanna Scassellati Sforzolini, Sabrina Pizzulo
Publikováno v:
Open Journal of Obstetrics and Gynecology. :735-739
In the last few decades, the use of ovarian stimulation with follicle stimulating hormone (FSH) or clomiphene citrate (CC) increases the percentage of multiple pregnancies. The presence of many follicles can lead to the risk of higher-order multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3ffed28027c1355891602dee708cd0c
https://doi.org/10.4236/ojog.2015.513103
https://doi.org/10.4236/ojog.2015.513103
Autor:
Carmelilia De Bernardo, Giovanna Scassellati Sforzolini, Daniela D'Angelantonio, Silvia Morlino, Irene Bottillo, Marco Castori, Paola Grammatico, Evelina Silvestri
Publikováno v:
Molecular Syndromology. 5:241-244
Nager syndrome, or acrofacial dysostosis type 1 (AFD1), is a rare multiple malformation syndrome characterized by hypoplasia of first and second branchial arches derivatives and appendicular anomalies with variable involvement of the radial/axial ray
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0a1c711388b526bae4ab3129b26aa6b
https://doi.org/10.1159/000365769
https://doi.org/10.1159/000365769
Autor:
Silvia, Morlino, Marco, Castori, Francesca, Servadei, Luigi, Laino, Evelina, Silvestri, Giovanna Scassellati, Sforzolini
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 103(6)
Oropharyngeal teratoma may occur by itself or together with other craniofacial malformations, most commonly cleft palate. Oropharyngeal teratoma may be also seen in association with frontonasal dysplasia and/or various degrees of craniofacial duplica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::635f070a0f8f1e44313ce563f72bc469
https://pubmed.ncbi.nlm.nih.gov/25360518
https://pubmed.ncbi.nlm.nih.gov/25360518
Autor:
S Cappellacci, Paola Grammatico, Francesco Binni, Giovanna Scassellati Sforzolini, Marco Castori, Evelina Silvestri
Publikováno v:
American journal of medical genetics. Part A. (7)
Sirenomelia and VACTERL association are defects of blastogenesis of unknown cause. Although they appear clinically distinct, some epidemiological and experimental studies suggest a common pathogenetic mechanism. We report on the reproductive history
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b9377b6a40f1973911ccc3fe86e6275
https://pubmed.ncbi.nlm.nih.gov/20583159
https://pubmed.ncbi.nlm.nih.gov/20583159