Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Emma Bertucci"'
Autor:
Neil Marlow, Luigi Raio, Roland Devlieger, Aris Papageorghiou, Rebecca Cannings-John, Christoph C Lees, Andrew Breeze, Andrew Sharp, Wessel Ganzevoort, Jim G Thornton, Julia Townson, Tanja Groten, Irene Cetin, Peter Lindgren, Federico Prefumo, Edward Mullins, Astrid Berger, Sofia Amylidi-Mohr, Cathrine Ebbing, Ladislav Krofta, Bianca Masturzo, Amarnath Bhide, Hans Wolf, Tiziana Frusca, Kurt Hecher, Tullio Ghi, Silvia Salvi, Wilfried Gyselaers, Raffaele Napolitano, MARK KILBY, Erich Cosmi, Claire Potter, Enrico Ferrazzi, Basky Thilaganathan, Dietmar Schlembach, Christine Morfeld, Bronacha Mylrea-Foley, Christina Ammari, Birgit Arabin, Eva Bergman, Caterina Bilardo, Julia Binder, Jana Brodszki, Pavel Calda, Andrej Černý, Elena Cesari, Andrea Dall'Asta, Anke Diemert, Torbjørn Eggebø, Ilaria Fantasia, Jenny Goodier, Patrick Greimel, Wassim Hassan, Constantin Von Kaisenberg, Alexey Kholin, Philipp Klaritsch, Silvia Lobmaier, Karel Marsal, Giuseppe M Maruotti, Federico Mecacci, Kirsti Myklestad, Eva Ostermayer, Jute Richter, Ragnar Kvie Sande, Ekkehard Schleußner, Tamara Stampalija, Herbert Valensise, Gerard HA Visser, Ling Wee, Andy Simm, Angela Ramoni, Barry Lloyd, Christopher Lloyd, Claudia Seidig, Danielle Thornton, Elena Mantovani, Emanuela Taricco, Emma Bertucci, Ferenc Macsali, Francesca Ferrari, Francesco D'Antonio, Giuseppe Cali, Giuseppe Rizzo, Ilaria Giuditta Ramezzana, Ioannis Kyvernitakis, Karen Melchiorre, Kristiina Rull, Laura Sarno, Liina Rajasalu, Louisa Jones, Makrina Savvidou, Maria Stefopoulou, Nicola Fratelli, Nishigandh Deole, Petra Pateisky, Pilar Palmrich, Ralf Schild, Sabina Ondrová, Sarah Gumpert, Serena Simeone, Silvia Visentin, Stefan Verlohren, Tatjana Radaelli, Tinne Mesens, Tiziana Fanelli, Yvonne Heiman, Zulfiya Khodzhaeva, Christoph Brezinka, Sanne Gordijn, Abin Thomas, Ligita Jokubkiene
Publikováno v:
BMJ Open, Vol 12, Iss 4 (2022)
Introduction Following the detection of fetal growth restriction, there is no consensus about the criteria that should trigger delivery in the late preterm period. The consequences of inappropriate early or late delivery are potentially important yet
Externí odkaz:
https://doaj.org/article/9633840173034347bd0a49beb46a528a
Autor:
Francesca Casciaro, Francesca Beretti, Martina Gatti, Giuseppe Persico, Emma Bertucci, Marco Giorgio, Tullia Maraldi
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 430 (2023)
Human amniotic fluid cells (hAFSCs) are a fascinating foetal cell-type that have important stem cell characteristics; however, they are a heterogeneous population that ranges from totally differentiated or progenitor cells to highly multipotent stem
Externí odkaz:
https://doaj.org/article/52d6f28fa4414a68a7861e7893533ab5
Autor:
Gianluca Di Massa, Guglielmo Stabile, Federico Romano, Andrea Balduit, Alessandro Mangogna, Beatrice Belmonte, Pina Canu, Emma Bertucci, Giuseppe Ricci, Tiziana Salviato
Publikováno v:
Medicina, Vol 57, Iss 2, p 162 (2021)
Background: Placental chorioangioma is the most common benign non-trophoblastic neoplasm of the placenta. Its clinical relevance lies in the size of the tumor since larger masses cause pregnancy complications, including an unfavorable neonatal outcom
Externí odkaz:
https://doaj.org/article/91c4dd04a9d244149cc8e592b687066a
Autor:
Francesca Casciaro, Silvia Zia, Mattia Forcato, Manuela Zavatti, Francesca Beretti, Emma Bertucci, Andrea Zattoni, Pierluigi Reschiglian, Francesco Alviano, Laura Bonsi, Matilde Yung Follo, Marco Demaria, Barbara Roda, Tullia Maraldi
Publikováno v:
Cells, Vol 10, Iss 1, p 158 (2021)
Human amniotic fluid stem cells (hAFSCs) are broadly multipotent immature progenitor cells with high self-renewal and no tumorigenic properties. These cells, even amplified, present very variable morphology, density, intracellular composition and ste
Externí odkaz:
https://doaj.org/article/50f90c607e4541b680c03c88f2444f71
Autor:
Vincenzo Mazza, Emma Bertucci, Silvia Latella, Carlotta Cani, Pierluca Ceccarelli, Lorenzo Iughetti, Fulvia Baldinotti, Antonio Percesepe
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2013 (2013)
Objectives. To demonstrate the feasibility of the prenatal diagnosis of partial androgen insensitivity syndrome by 3D-4D ultrasound. Methods. To report prenatal diagnosis of partial androgen insensitivity syndrome at 32nd week of gestation by 3D-4D u
Externí odkaz:
https://doaj.org/article/00fb0a83080046dbad6003c7c7ed8e55
Autor:
Emma Bertucci, Filomena G. Sileo, Marialaura Diamanti, Carlo Alboni, Fabio Facchinetti, Antonio La Marca
Publikováno v:
International Journal of Gynecology & Obstetrics. 160:856-863
To study how adenomyosis changes during pregnancy and to possibly correlate these changes to maternal and fetal outcomes.Retrospective exploratory cohort study including 254 women with a pre-conceptional/first-trimester scan to document adenomyosis a
Autor:
Sara De Biasi, Anita Neroni, Milena Nasi, Domenico Lo Tartaro, Rebecca Borella, Lara Gibellini, Laura Lucaccioni, Emma Bertucci, Licia Lugli, Francesca Miselli, Luca Bedetti, Isabella Neri, Fabrizio Ferrari, Fabio Facchinetti, Alberto Berardi, Andrea Cossarizza
Publikováno v:
European Journal of Immunology. 53
Autor:
Francesca Monari, Daniela Menichini, Emma Bertucci, Isabella Neri, Enrica Perrone, Fabio Facchinetti
Publikováno v:
International Journal of Gynecology & Obstetrics. 159:810-816
To investigate the effect of a quality improvement project with an educational/motivational intervention in northern Italy on the implementation of the trial of labor after cesarean section (CS).A pre-post study design was used. Every birth center (n
Autor:
null Sara De Biasi, null Anita Neroni, null Milena Nasi, null Domenico Lo Tartaro, null Rebecca Borella, null Lara Gibellini, null Laura Lucaccioni, null Emma Bertucci, null Licia Lugli, null Francesca Miselli, null Luca Bedetti, null Isabella Neri, null Fabrizio Ferrari, null Fabio Facchinetti, null Alberto Berardi, null Andrea Cossarizza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7ce8dc3c37aefbd3bec694250725bb6
https://doi.org/10.1002/eji.202250224/v2/response1
https://doi.org/10.1002/eji.202250224/v2/response1
Autor:
Sara Pini, Floriana Maria Napoli, Enrico Tagliafico, Antonio La Marca, Emma Bertucci, Valentina Salsi, Rossella Tupler
Publikováno v:
Clinical geneticsREFERENCES.
Facioscapulohumeral muscular dystrophy (FSHD) has been associated with the deletion of an integral number of 3.3 kb units of the polymorphic D4Z4 repeat array at 4q35. The prenatal identification of this defect can be carried out on chorionic villi o