Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Valeria Polizzi"'
Autor:
Elisabetta Genovese, Silvia Palma, Valeria Polizzi, Giovanni Bianchin, Michela Cappai, Shaniko Kaleci, Alessandro Martini, Andrea Ciorba, Paolo Stagi
Publikováno v:
Audiology Research, Vol 11, Iss 3, Pp 463-473 (2021)
Hearing loss is one of the most common congenital sensory disorders. It can be associated with several comorbidities, in particular developmental disabilities (DD). In Emilia-Romagna (ER), a region in Northern Italy, Child and Adolescent Mental Healt
Externí odkaz:
https://doaj.org/article/07fe4f0d6aff4d6abaf8850443edb018
Autor:
Enrico Apa, Maria Teresa Presutti, Cecilia Rossi, Maria Federica Roversi, Salvatore Neri, Giancarlo Gargano, Giovanni Bianchin, Valeria Polizzi, Valeria Caragli, Daniele Monzani, Alberto Berardi, Silvia Palma, Elisabetta Genovese
Publikováno v:
Children, Vol 10, Iss 2, p 194 (2023)
Background: Gestational SARS-CoV-2 infection can impact maternal and neonatal health. The virus has also been reported to cause newborn sensorineural hearing loss, but its consequences for the auditory system are not fully understood. Objective: The
Externí odkaz:
https://doaj.org/article/0eee8a7088d44b5087be6ac60f47624a
Publikováno v:
Case Reports in Otolaryngology, Vol 2016 (2016)
Externí odkaz:
https://doaj.org/article/6acbf073ab9c452abf35a8aa28ea2811
Publikováno v:
Case Reports in Otolaryngology, Vol 2015 (2015)
We describe the novel solution adopted in positioning middle ear implant in a child with bilateral congenital aural atresia and craniofacial dysmorphism that have posed a significant challenge for the safe and correct management of deafness. A five-y
Externí odkaz:
https://doaj.org/article/610a5610822a43eeab4cff30af1901b3
Autor:
Giovanni Bianchin, Shaniko Kaleci, Alessandro Martini, Andrea Ciorba, Silvia Palma, Valeria Polizzi, Elisabetta Genovese, Michela Cappai, Paolo Stagi
Publikováno v:
Audiology Research
Volume 11
Issue 3
Pages 43-473
Audiology Research, Vol 11, Iss 43, Pp 463-473 (2021)
Volume 11
Issue 3
Pages 43-473
Audiology Research, Vol 11, Iss 43, Pp 463-473 (2021)
Hearing loss is one of the most common congenital sensory disorders. It can be associated with several comorbidities, in particular developmental disabilities (DD). In Emilia-Romagna (ER), a region in Northern Italy, Child and Adolescent Mental Healt
Autor:
Ivan Ivanovski, Raoul C.M. Hennekam, Valeria Polizzi, Mahboubeh Mansouri, Livia Garavelli, Marzia Pollazzon, Marielle Alders, Zahra Chavoshzadeh, Susan Akbaroghli, Simonetta Rosato, Stefano Giuseppe Caraffi, Giancarlo Gargano, Chiara Gelmini
Publikováno v:
American journal of medical genetics. Part A, 176(5), 1166-1174. Wiley-Liss Inc.
Biallelic variants in FAT4 are associated with the two disorders, Van Maldergem syndrome (VMS) (n = 11) and Hennekam syndrome (HS) (n= 40). Both conditions are characterized by a typical facial gestalt and mild to moderate intellectual disability, bu
Publikováno v:
International journal of pediatric otorhinolaryngology. 102
Objective To examine speech intelligibility in children subjected to sequential bilateral cochlear implants (CI) surgery and to assess the influence of the inter-stage interval duration. Introduction Binaural hearing recovery can have additional bene
Publikováno v:
Case Reports in Otolaryngology, Vol 2016 (2016)
Publikováno v:
International Journal of Otolaryngology, Vol 2016 (2016)
International Journal of Otolaryngology
International Journal of Otolaryngology
Objective. To share our experience of cerebrospinal fluid gusher in cochlear implantation in patients with enlarged cochlear or vestibular aqueduct.Study Design. Case series with comparison and a review of the literature.Methods. A retrospective stud
Publikováno v:
Case Reports in Otolaryngology
Case Reports in Otolaryngology, Vol 2016 (2016)
Case Reports in Otolaryngology, Vol 2015 (2015)
Case Reports in Otolaryngology, 2016, pp. 2859051
Case Reports in Otolaryngology, 2016, 2859051
Case Reports in Otolaryngology, Vol 2016 (2016)
Case Reports in Otolaryngology, Vol 2015 (2015)
Case Reports in Otolaryngology, 2016, pp. 2859051
Case Reports in Otolaryngology, 2016, 2859051
With great interest we read the recently published article by Bianchin et al. describing a case report of a child with Van Maldergem Syndrome causing severe craniofacial dysmorphism and bilateral congenital conductive hearing loss due to microtia and