Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Emilio Amilibia"'
Autor:
Núria Catasús, Miguel Torres-Martin, Alex Negro, Bernd Kuebler, Inma Rosas, Gemma Casals, Helena Mazuelas, Francesc Roca-Ribas, Emilio Amilibia, Begoña Aran, Anna Veiga, Ángel Raya, Bernat Gel, Ignacio Blanco, Eduard Serra, Meritxell Carrió, Elisabeth Castellanos
BackgroundThe appearance of bilateral vestibular schwannomas (VS) is one of the most characteristic features of NF2-related schwannomatosis (NF2-related SWN), an autosomal dominant syndrome that predisposes to the development of tumours of the nervou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95fb83bde98ce60f26ac3789a4b23af5
https://doi.org/10.1101/2022.12.14.520389
https://doi.org/10.1101/2022.12.14.520389
Autor:
Alberto F. Maroto, Mireia Borrajo, Sílvia Prades, Àngela Callejo, Emilio Amilibia, Marta Pérez-Grau, Francesc Roca-Ribas, Elisabeth Castellanos, Alejandro Barrallo-Gimeno, Jordi Llorens
Hair cell (HC) loss by epithelial extrusion has been described to occur in the rodent vestibular system during chronic 3,3′-iminodipropionitrile (IDPN) ototoxicity. This is preceded by dismantlement of the calyceal junction in the contact between t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb13fd983062eb2ecf7f152e7256d0d
https://doi.org/10.1101/2022.05.17.492294
https://doi.org/10.1101/2022.05.17.492294
Autor:
Alejandro Negro, Cristina Hostalot, Juan Luis Becerra, Conxi Lazaro Garcia, Adrià Plana, Eduard Serra, Belen Garcia, Ignacio Blanco, Núria Catasús, Iván Galván-Femenía, Rafael de Cid, Andrea Ros, Isabel Bielsa, Elisabeth Castellanos, Emilio Amilibia, Inma Rosas, Francesc Roca-Ribas
Publikováno v:
Journal of Medical Genetics
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
BackgroundNeurofibromatosis type 2 (NF2) is an autosomal dominant disorder characterised by the development of multiple schwannomas, especially on vestibular nerves, and meningiomas. The UK NF2 Genetic Severity Score (GSS) is useful to predict the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::187d539054969332edec3f44baf86262
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=1742
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=1742
Autor:
Carme Moragues Pastor, Emilio Amilibia Cabeza, Susana Holgado Pérez, Miquel Quer Agustí, Francesc Roca-Ribas Serdà, Marta Pérez Grau
Publikováno v:
Acta Otorrinolaringologica (English Edition). 70:89-96
Introduction and objectives Paget's disease of bone (PDB) may lead to hearing loss. The present study was conducted with the aim of measuring, characterising and determining the risk factors for hearing loss in a group of subjects with PDB. Methods A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e5b2b0626204e3b62388c3bda2cacc4
https://doi.org/10.1016/j.otoeng.2019.03.003
https://doi.org/10.1016/j.otoeng.2019.03.003
Autor:
Francesc Roca-Ribas Serdà, Emilio Amilibia Cabeza, Susana Holgado Pérez, Miquel Quer Agustí, Carme Moragues Pastor, Marta Pérez Grau
Publikováno v:
Acta Otorrinolaringológica Española. 70:89-96
Resumen Introduccion y objetivos La enfermedad osea de Paget (EOP) puede cursar con hipoacusia. Con el objetivo de cuantificar, caracterizar y determinar los factores de riesgo de hipoacusia en un grupo de pacientes con EOP se realiza el presente est
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb5e98254d5b2f96cc7fe073666178a4
https://doi.org/10.1016/j.otorri.2018.04.002
https://doi.org/10.1016/j.otorri.2018.04.002
Autor:
Francesc Roca-Ribas, Paloma Puyalto, Marta Pérez-Grau, Àngela Callejo, Patricia Cuadras, Emilio Amilibia
Publikováno v:
OTOLOGY & NEUROTOLOGY
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Objectives: To study computed tomography findings in Paget's disease of temporal bone (PDTB) and analyze the relations between otic capsule bone mineral density values measured in Hounsfield Units (HU) and hearing loss (HL). Study Design: Observation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86d1045be434bdde43cc7948864b88ae
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=1665
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=1665
Autor:
Cristina Hostalot, Emilio Amilibia, Francesc Roca-Ribas, R. de Cid, Adrià Plana, Eduard Serra, Isabel Bielsa, Andrea Ros, N. Catasús, Conxi Lázaro, Alejandro Negro, Jl. Becerra, Ignacio Blanco, Belen Garcia, Elisabeth Castellanos, Inma Rosas, I. Galvan
BackgroundNeurofibromatosis Type 2 (NF2) is an autosomal dominant disorder characterized by the development of multiple schwannomas, particularly at vestibular nerves, and meningiomas. The UK NF2 Genetic Severity Score (GSS) helps predicting the dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d801670d21a6fb3b66525578868e2ee3
https://doi.org/10.1101/2020.10.22.20216614
https://doi.org/10.1101/2020.10.22.20216614
Autor:
Francesc Roca-Ribas, Marta Pérez, Javier Gavilán, Emilio Amilibia, Ruben Polo, Alfonso Muriel, Luis Lassaletta, María del Mar Medina, Ignacio Cobeta, Miguel Díaz
Publikováno v:
Ear and Hearing
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Objectives: Cochlear implants (CIs) are a well-known hearing restoration option for patients with vestibular schwannoma (VS) in cases of neurofibromatosis type-2 and, more recently, for patients with sporadic VS. One of the main limitations when perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f68ffd5c78151de5c34bd5e5a73d57
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4161
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4161
Autor:
Conxi Lázaro, Ariadna Quer, Alicia Castillo, Meritxell Carrió, Cristina Hostalot, Juan Luis Becerra, Elisabeth Castellanos, Andrea Ros, Adrià Plana, Inma Rosas, Ignacio Blanco, Isabel Bielsa, Francesc Roca-Ribas, Eduard Serra, Cristina Carrato, for Csur Phakomatoses Multidisciplinary Clinics HUGTiP-ICO-IGTP, Emilio Amilibia, Hector Salvador
Publikováno v:
JAMA Dermatol
Importance Neurofibromatosis type 2 (NF2) is a devastating genetic condition characterized by the development of multiple tumors of the nervous system. An early diagnosis of individuals with NF2 would facilitate treatment and reduction of disease imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::973671d60777de0bcc405799183b697e
https://pubmed.ncbi.nlm.nih.gov/29998308
https://pubmed.ncbi.nlm.nih.gov/29998308
Publikováno v:
ORL. 60:227-229
Bilateral facial nerve palsy is relatively uncommon and may occur in association with a variety of neurological, infectious, neoplastic or degenerative disorders. Presentation is made of 4 cases of bilateral facial diplegia due to a refractory anemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4850d85b8b25935cf5f1675a2dcdc09
https://doi.org/10.1159/000027599
https://doi.org/10.1159/000027599