Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Romolo Daniele De Siati"'
Autor:
Laurence Jonard, Davide Brotto, Miguel A. Moreno-Pelayo, Ignacio del Castillo, Hannie Kremer, Ronald Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Publikováno v:
Audiology Research, Vol 13, Iss 3, Pp 341-346 (2023)
The cause of childhood hearing impairment (excluding infectious pathology of the middle ear) can be extrinsic (embryofoetopathy, meningitis, trauma, drug ototoxicity, noise trauma, etc [...]
Externí odkaz:
https://doaj.org/article/1f272fa0e4ba4f1d9885851b72d3604b
Autor:
Giulia Crispino, Giovanni Di Pasquale, Pietro Scimemi, Laura Rodriguez, Fabian Galindo Ramirez, Romolo Daniele De Siati, Rosa Maria Santarelli, Edoardo Arslan, Mario Bortolozzi, John A Chiorini, Fabio Mammano
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23279 (2011)
The deafness locus DFNB1 contains GJB2, the gene encoding connexin26 and GJB6, encoding connexin30, which appear to be coordinately regulated in the inner ear. In this work, we investigated the expression and function of connexin26 and connexin30 fro
Externí odkaz:
https://doaj.org/article/f7d65068302f431e8428757bfc8a5321
Autor:
Romolo Daniele De Siati, Chiara Gallo, Giacomo Spinato, Andrea Frosolini, Cosimo de Filippis, Daniela Parrino
Publikováno v:
International journal of audiology, Vol. 61, no.6, p. 526-529 (2022)
Objective To ensure the safety and quality of vaccines, especially the newest RNA-vaccines against COVID-19, is one of the World Health Organization's current highest priorities. Design Case description. Study sample We report three cases of sudden u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42e96982a6afad5f5565f5ab6fa8d13
https://pubmed.ncbi.nlm.nih.gov/34120553
https://pubmed.ncbi.nlm.nih.gov/34120553
Autor:
Naima Deggouj, Elsa Wiame, Antonella Boschi, Marie-Cécile Nassogne, Stéphanie Paquay, Romolo Daniele De Siati, Yves Sznajer
Publikováno v:
International Journal of Pediatric Otorhinolaryngology, Vol. 104, p. 191-194 (2018)
CAPOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss) is a rare neurological disorder, recently associated with the c.2452G > A hotspot mutation in the ATP1A3 gene, with sensorineural hearing loss as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c3dc5eaa2c69180405c8f3119e4326b
https://doi.org/10.1016/j.ijporl.2017.11.022
https://doi.org/10.1016/j.ijporl.2017.11.022
Akademický článek
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Autor:
Flora Rosenzweig, Philippe Rombaux, Romolo Daniele De Siati, Anaïs Grégoire, Guillaume Gersdorff, Naima Deggouj
Publikováno v:
Journal of clinical medicine, Vol. 9, no.4, p. 1-29 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 1074, p 1074 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 1074, p 1074 (2020)
Auditory neuropathy spectrum disorder (ANSD) refers to a range of hearing impairments characterized by deteriorated speech perception, despite relatively preserved pure-tone detection thresholds. Affected individuals usually present with abnormal aud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb666dd20c6c82978a6b76e47fff5f39
https://doi.org/10.3390/jcm9041074
https://doi.org/10.3390/jcm9041074
Autor:
Romolo Daniele De Siati, Karen Spruyt, Catherine Vanderveken, Jennifer Petrossi, Maria Pia Bucci, Sylvette Wiener-Vacher, Michel Debue, Hung Thai-Van, Naima Deggouj, Nathalie Goulème, José Ortega-Solis, E. Ionescu
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 2018, 113, pp.272-280. ⟨10.1016/j.ijporl.2018.08.005⟩
International journal of pediatric otorhinolaryngology, Vol. 113, p. 272-280 (2018)
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2018, 113, pp.272-280. ⟨10.1016/j.ijporl.2018.08.005⟩
International Journal of Pediatric Otorhinolaryngology, 2018, 113, pp.272-280. ⟨10.1016/j.ijporl.2018.08.005⟩
International journal of pediatric otorhinolaryngology, Vol. 113, p. 272-280 (2018)
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2018, 113, pp.272-280. ⟨10.1016/j.ijporl.2018.08.005⟩
International audience; Background: The aim of this multicenter study is to investigate the effect of chronological age and gender in postural control.Methods: To approach an ecological model, we used a multicenter posturography assessment. We analyz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b630c4f9ed7b964c1d551fb2f9910a4
https://hal.parisnanterre.fr/hal-03151002/file/Goulemeetal_2019.pdf
https://hal.parisnanterre.fr/hal-03151002/file/Goulemeetal_2019.pdf
Autor:
Saida Ortolano, Andrew Parker, Pietro Scimemi, Giulia Crispino, Marisa Brini, Ernesto Carafoli, Steve D.M. Brown, Francesca Di Leva, Fabio Mammano, Edoardo Arslan, Nicholas J. Parkinson, Mario Bortolozzi, Romolo Daniele De Siati
Publikováno v:
The Journal of Biological Chemistry
The mechanotransduction process in hair cells in the inner ear is associated with the influx of calcium from the endolymph. Calcium is exported back to the endolymph via the splice variant w/a of the PMCA2 of the stereocilia membrane. To further inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcdf8c64dbcf353e5daf64d60c988c41
https://doi.org/10.1074/jbc.m110.170092
https://doi.org/10.1074/jbc.m110.170092
Autor:
Klaus Willecke, Romolo Daniele De Siati, Karen P. Steel, Stephan Sonntag, Laura Zúñiga Rodríguez, Fabio Mammano, Mario Bortolozzi, Melanie Schütz, Pietro Scimemi, Anke Seydel, Giulia Crispino, Rosamaria Santarelli, Neil J. Ingham, Paromita Majumder
Publikováno v:
Human Molecular Genetics
Mutations in the GJB2 and GJB6 genes, respectively, coding for connexin26 (Cx26) and connexin30 (Cx30) proteins, are the most common cause for prelingual non-syndromic deafness in humans. In the inner ear, Cx26 and Cx30 are expressed in different non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a3bbd14c405d4c3d13b587f4ee97117
https://doi.org/10.1093/hmg/ddq402
https://doi.org/10.1093/hmg/ddq402
Autor:
Laura Rodriguez, John A. Chiorini, Mario Bortolozzi, Giovanni Di Pasquale, Fabio Mammano, Pietro Scimemi, Giulia Crispino, Edoardo Arslan, Rosamaria Santarelli, Fabian Galindo Ramirez, Romolo Daniele De Siati
Publikováno v:
PloS one 6 (2011). doi:10.1371/journal.pone.0023279
info:cnr-pdr/source/autori:Crispino, Giulia; Di Pasquale, Giovanni; Scimemi, Pietro; Rodriguez, Laura; Ramirez, Fabian Galindo; De Siati, Romolo Daniele; Santarelli, Rosa Maria; Arslan, Edoardo; Bortolozzi, Mario; Chiorini, John A.; Mammano, Fabio/titolo:BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice/doi:10.1371%2Fjournal.pone.0023279/rivista:PloS one/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume:6
PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e23279 (2011)
info:cnr-pdr/source/autori:Crispino, Giulia; Di Pasquale, Giovanni; Scimemi, Pietro; Rodriguez, Laura; Ramirez, Fabian Galindo; De Siati, Romolo Daniele; Santarelli, Rosa Maria; Arslan, Edoardo; Bortolozzi, Mario; Chiorini, John A.; Mammano, Fabio/titolo:BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice/doi:10.1371%2Fjournal.pone.0023279/rivista:PloS one/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume:6
PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e23279 (2011)
The deafness locus DFNB1 contains GJB2, the gene encoding connexin26 and GJB6, encoding connexin30, which appear to be coordinately regulated in the inner ear. In this work, we investigated the expression and function of connexin26 and connexin30 fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::044aa951e9072ae891d26f1771943dfc
http://hdl.handle.net/11577/2477966
http://hdl.handle.net/11577/2477966