Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Elisa Bet"'
Autor:
Lorenzo Monasta, Manuela Giangreco, Emanuele Ancona, Fabio Barbone, Elisa Bet, Pierino Boschian-Bailo, Giovanna Cacciaguerra, Angelo Cagnacci, Melania Canton, Maddalena Casarotto, Manola Comar, Simona Contardo, Michela De Agostini, Francesco De Seta, Giovanni Del Ben, Carla Di Loreto, Lorenza Driul, Stefano Facchin, Roberta Giornelli, Annalisa Ianni, Santo La Valle, Ambrogio Pietro Londero, Marciano Manfè, Gianpaolo Maso, Raffaela Mugittu, Monica Olivuzzi, Maria Orsaria, Vanna Pecile, Roberta Pinzano, Francesco Pirrone, Mariachiara Quadrifoglio, Giuseppe Ricci, Luca Ronfani, Tiziana Salviato, Elisa Sandrigo, Silvia Smiroldo, Alice Sorz, Tamara Stampalija, Marianela Urriza, Michele Vanin, Giuseppina Verardi, Salvatore Alberico
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background Intrauterine fetal death (IUFD) is a tragic event and, despite efforts to reduce rates, its incidence remains difficult to reduce. The objective of the present study was to examine the etiological factors that contribute to the ma
Externí odkaz:
https://doaj.org/article/ffd069ea6f44461c92de98b4fd4b5041
Autor:
Daniel Gaspar, Catarina Ginja, Nuno Carolino, Célia Leão, Helena Monteiro, Lino Tábuas, Sandra Branco, Ludovina Padre, Pedro Caetano, Ricardo Romão, Claudino Matos, António Marcos Ramos, Elisa Bettencourt, Ana Usié
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Ovine footrot caused by Dichelobacter nodosus (D. nodosus) is a contagious disease with serious economic and welfare impacts in sheep production systems worldwide. A better understanding of the host genetic architecture regarding
Externí odkaz:
https://doaj.org/article/1b9bced1df484813a3cc593c74a629e1
Autor:
Daniel Gaspar, Catarina Ginja, Nuno Carolino, Célia Leão, Helena Monteiro, Lino Tábuas, Sandra Branco, Ludovina Padre, Pedro Caetano, Ricardo Romão, Claudino Matos, António Marcos Ramos, Elisa Bettencourt, Ana Usié
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/431e296ff9ad4a5b951f94b593b1e3ec
Publikováno v:
Buildings, Vol 13, Iss 4, p 979 (2023)
This paper intends to deepen the topic of damage detection based on non-destructive tests (NDT) for the assessment of the dynamic behavior of RC beams damaged and strengthened both with near-surface mounted (NSM) Carbon and GlassFRP rods. The NSM str
Externí odkaz:
https://doaj.org/article/a3044894faaa468084e1072b8fc20a1d
Autor:
Hui Guo, Elisa Bettella, Paul C. Marcogliese, Rongjuan Zhao, Jonathan C. Andrews, Tomasz J. Nowakowski, Madelyn A. Gillentine, Kendra Hoekzema, Tianyun Wang, Huidan Wu, Sharayu Jangam, Cenying Liu, Hailun Ni, Marjolein H. Willemsen, Bregje W. van Bon, Tuula Rinne, Servi J. C. Stevens, Tjitske Kleefstra, Han G. Brunner, Helger G. Yntema, Min Long, Wenjing Zhao, Zhengmao Hu, Cindy Colson, Nicolas Richard, Charles E. Schwartz, Corrado Romano, Lucia Castiglia, Maria Bottitta, Shweta U. Dhar, Deanna J. Erwin, Lisa Emrick, Boris Keren, Alexandra Afenjar, Baosheng Zhu, Bing Bai, Pawel Stankiewicz, Kristin Herman, University of Washington Center for Mendelian Genomics, Saadet Mercimek-Andrews, Jane Juusola, Amy B. Wilfert, Rami Abou Jamra, Benjamin Büttner, Heather C. Mefford, Alison M. Muir, Ingrid E. Scheffer, Brigid M. Regan, Stephen Malone, Jozef Gecz, Jan Cobben, Marjan M. Weiss, Quinten Waisfisz, Emilia K. Bijlsma, Mariëtte J. V. Hoffer, Claudia A. L. Ruivenkamp, Stefano Sartori, Fan Xia, Jill A. Rosenfeld, Raphael A. Bernier, Michael F. Wangler, Shinya Yamamoto, Kun Xia, Alexander P. A. Stegmann, Hugo J. Bellen, Alessandra Murgia, Evan E. Eichler
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
Neurodevelopmental disorders (NDDs) are a heterogeneous group of diseases for which the genetic basis is still unknown in more than half of the cases. Here, the authors report a NDD associated with disruptive variants in the TANC2 gene and show that
Externí odkaz:
https://doaj.org/article/663adb56ce6f405da787645af9303af8
Autor:
Emanuela Leonardi, Elisa Bettella, Maria Federica Pelizza, Maria Cristina Aspromonte, Roberta Polli, Clementina Boniver, Stefano Sartori, Donatella Milani, Alessandra Murgia
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
SETBP1 mutations are associated with the Schinzel-Giedion syndrome (SGS), characterized by profound neurodevelopmental delay, typical facial features, and multiple congenital malformations (OMIM 269150). Refractory epilepsy is a common feature of SGS
Externí odkaz:
https://doaj.org/article/4eafa9de15244dd99f166bf566148d99
Autor:
Giacomo Farì, Alessandro de Sire, Cettina Fallea, Mariantonia Albano, Gianluca Grossi, Elisa Bettoni, Stefano Di Paolo, Francesco Agostini, Andrea Bernetti, Filomena Puntillo, Carlo Mariconda
Publikováno v:
Diagnostics, Vol 12, Iss 3, p 600 (2022)
Radiofrequency (RF) is a minimally invasive procedure used to interrupt or alter nociceptive pathways for treating musculoskeletal pain. It seems a useful tool to relieve chronic pain syndromes, even if, to date, solid evidence is still needed about
Externí odkaz:
https://doaj.org/article/24758b47c3cf408fb68db7bdf28beed0
Autor:
Emanuela Leonardi, Mariagrazia Bellini, Maria C. Aspromonte, Roberta Polli, Anna Mercante, Claudia Ciaccio, Elisa Granocchio, Elisa Bettella, Ilaria Donati, Elisa Cainelli, Stefania Boni, Stefano Sartori, Chiara Pantaleoni, Clementina Boniver, Alessandra Murgia
Publikováno v:
Genes, Vol 11, Iss 3, p 344 (2020)
WAC (WW Domain Containing Adaptor With Coiled-Coil) mutations have been reported in only 20 individuals presenting a neurodevelopmental disorder characterized by intellectual disability, neonatal hypotonia, behavioral problems, and mildly dysmorphic
Externí odkaz:
https://doaj.org/article/47e3678fea654c90ac0b10967580b75a
Autor:
Micaela Fredi, Laura Andreoli, Elena Aggogeri, Elisa Bettiga, Maria Grazia Lazzaroni, Véronique Le Guern, Andrea Lojacono, Nathalie Morel, Jean Charles Piette, Sonia Zatti, Nathalie Costedoat-Chalumeau, Angela Tincani
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
ObjectiveAntiphospholipid antibodies positivity (aPL) is considered as a risk factor for adverse pregnancy outcome (APO). The aim of this study was to determine the risk factors for APO in patients with confirmed aPL positivity, isolated (aPL carrier
Externí odkaz:
https://doaj.org/article/6d737366fe75421f889d0d919314dd9f
Publikováno v:
Proceedings, Vol 1, Iss 9, p 934 (2017)
Landscape is born when a place is felt, lived, suffered, owned, when it is perceived, in the etymological sense, for which it is taken what is conveyed by the vision with an aim (per-ceive). The underlying theory is related to its etymological link w
Externí odkaz:
https://doaj.org/article/7c7cc10a9d1a4344a51f3bc759c9613b