Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Jessica, Galli"'
Autor:
Pablo Iruzubieta, César Augusto Pinheiro Ferreira Alves, Aisha M. Al Shamsi, Gehad ElGhazali, Maha S. Zaki, Lorenzo Pinelli, Diego Lopergolo, Bernard P.H. Cho, Amy A. Jolly, Amna Al Futaisi, Fatema Al-Amrani, Jessica Galli, Elisa Fazzi, Katarina Vulin, Francisco Barajas-Olmos, Holger Hengel, Bayan Mohammed Aljamal, Vahideh Nasr, Farhad Assarzadegan, Michele Ragno, Luigi Trojano, Naomi Meave Ojeda, Arman Çakar, Silvia Bianchi, Francesca Pescini, Anna Poggesi, Amal Al Tenalji, Majid Aziz, Rahema Mohammad, Aziza Chedrawi, Nicola De Stefano, Giovanni Zifarelli, Ludger Schöls, Tobias B. Haack, Adriana Rebelo, Stephan Zuchner, Filiz Koc, Lyn R. Griffiths, Lorena Orozco, Karla García Helmes, Meisam Babaei, Peter Bauer, Won Chan Jeong, Ehsan Ghayoor Karimiani, Miriam Schmidts, Joseph G. Gleeson, Wendy K. Chung, Fowzan Sami Alkuraya, Bita Shalbafan, Hugh S. Markus, Henry Houlden, Reza Maroofian
Publikováno v:
EBioMedicine, Vol 107, Iss , Pp 105297- (2024)
Summary: Background: NOTCH3 encodes a transmembrane receptor critical for vascular smooth muscle cell function. NOTCH3 variants are the leading cause of hereditary cerebral small vessel disease (SVD). While monoallelic cysteine-involving missense var
Externí odkaz:
https://doaj.org/article/dcf457b6550e45488640bb16d06d46d7
Autor:
Viola Oldrati, Verusca Gasparroni, Arianna Michelutti, Andrea Ciricugno, Renato Borgatti, Simona Orcesi, Elisa Fazzi, Alessandra Morandi, Jessica Galli, Luigi Piccinini, Cristina Maghini, Maria Arioli, Zaira Cattaneo, Cosimo Urgesi, Alessandra Finisguerra
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundGross motor function impairments and manual dexterity deficits are frequently observed in children and adolescents with Cerebral Palsy (CP), having a major impact on their activity level and autonomy. Improving manual dexterity and activity
Externí odkaz:
https://doaj.org/article/9b938afc2331411fbd66e8130d378e17
Autor:
Jessica Galli, Marco Cattalini, Erika Loi, Rosalba Monica Ferraro, Silvia Giliani, Simona Orcesi, Lorenzo Pinelli, Raffaele Badolato, Elisa Fazzi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message Baricitinib, a Janus kinase inhibitor (JAK‐inhibitor), seems to contribute to an improvement of a child affected by Aicardi‐Goutières syndrome (AGS), reducing the interferon score and determining a recovery of cognitive, com
Externí odkaz:
https://doaj.org/article/ce9d1c8917e54d20a9c225c03f5ebd97
Autor:
Marina A. Pavlova, Jessica Galli, Federica Zanetti, Federica Pagani, Serena Micheletti, Andrea Rossi, Alexander N. Sokolov, Andreas J. Fallgatter, Elisa M. Fazzi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Faces hold a substantial value for effective social interactions and sharing. Covering faces with masks, due to COVID-19 regulations, may lead to difficulties in using social signals, in particular, in individuals with neurodevelopmental con
Externí odkaz:
https://doaj.org/article/36f38ae980d649ceafb01c171e4b301f
Autor:
Jessica Galli, Gioacchino Garofalo, Sara Brunetti, Erika Loi, Michela Portesi, Giovanni Pelizzari, Andrea Rossi, Elisa Fazzi, Giovanni Buccino
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
The present study aimed at assessing whether children with Cerebral Palsy (CP) can imagine object directed actions similarly to their normally developed peers. We asked children with CP (n = 12) and paired healthy controls (n = 12) to imagine in firs
Externí odkaz:
https://doaj.org/article/4a0668882cee422c9a3eaac2a6828234
Autor:
Jessica Galli, Erika Loi, Anna Molinaro, Stefano Calza, Alessandra Franzoni, Serena Micheletti, Andrea Rossi, Francesco Semeraro, Elisa Fazzi, CP Collaborative Group
Publikováno v:
Frontiers in Human Neuroscience, Vol 16 (2022)
BackgroundCerebral Visual Impairment (CVI) is a very common finding in children affected by Cerebral Palsy (CP). In this paper we studied the characteristics of CVI of a large group of children with CP and CVI, describing their neurovisual profiles a
Externí odkaz:
https://doaj.org/article/97ef13147a514b71a77c2c13a7f9fd5d
Autor:
Jessica Galli, Erika Loi, Lucrezia Maria Visconti, Paola Mattei, Anna Eusebi, Stefano Calza, Elisa Fazzi, ASD Collaborative Group, Luisa Bonini, Angela Merlini, Laura Pansera, Laura Malerba, Filippo Gitti
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundSleep disturbances are common in children affected by Autism Spectrum Disorder (ASD). The aim of our study was to describe sleep characteristics and disturbances in children with ASD, to evaluate possible related factors, and to assess pare
Externí odkaz:
https://doaj.org/article/68d340a4529a4c76b719bdb80fe2f6a9
Autor:
Serena Micheletti, Fleur Corbett, Janette Atkinson, Oliver Braddick, Paola Mattei, Jessica Galli, Stefano Calza, Elisa Fazzi
Publikováno v:
Frontiers in Human Neuroscience, Vol 15 (2021)
Dorsal stream cortical networks underpin a cluster of visuomotor, visuospatial, and visual attention functions. Sensitivity to global coherence of motion and static form is considered a signature of visual cortical processing in the dorsal stream (mo
Externí odkaz:
https://doaj.org/article/31d1f9ba34e9455082f1cb336b7bbe3a
Autor:
Marco Cattalini, Jessica Galli, Fiammetta Zunica, Rosalba Monica Ferraro, Marialuisa Carpanelli, Simona Orcesi, Giovanni Palumbo, Lorenzo Pinelli, Silvia Giliani, Elisa Fazzi, Raffaele Badolato
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Type I Interferonopathies comprise inherited inflammatory diseases associated with perturbation of the type I IFN response. Use of Janus kinase (JAK) inhibitors has been recently reported as possible tools for treating some of those rare diseases. We
Externí odkaz:
https://doaj.org/article/fad05f27d2b8404c9df698e89f0c8232
Autor:
Jessica Galli, Lorenzo Pinelli, Serena Micheletti, Giovanni Palumbo, Lucia Dora Notarangelo, Vassilios Lougaris, Laura Dotta, Elisa Fazzi, Raffaele Badolato
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Warts Hypogammaglobulinemia Immunodeficiency Myelokathexis (WHIM) syndrome is a primary immunodeficiency characterized by recurrent bacterial infections, severe chronic neutropenia, with lymphopenia, monocytopenia and myelokathexi
Externí odkaz:
https://doaj.org/article/7240e706dfe24179aaf0127aea415ee2