Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Piedad García-Díaz"'
Autor:
Ma Piedad García Díaz, Lidia Torres-García, Enrique García Zamora, Ana Belén Castilla Jiménez, Vanesa Pérez Guillén
Publikováno v:
Audiology Research, Vol 12, Iss 2, Pp 126-131 (2022)
The aim of this study was to evaluate the vestibulo-ocular reflex (VOR) gain and the saccade regrouping pattern PR score of the Video Head Impulse Test (vHIT) and its relationship with the slow-phase velocity (SPV) of skull vibration-induced nystagmu
Externí odkaz:
https://doaj.org/article/632c682dad8e4cf4b4974710d05aa68c
Autor:
Ma Piedad García Díaz, Lidia Torres-García, Enrique García Zamora, Ana Belén Castilla Jiménez, Vanesa Pérez Guillén
Publikováno v:
Audiology Research; Volume 12; Issue 2; Pages: 126-131
The aim of this study was to evaluate the vestibulo-ocular reflex (VOR) gain and the saccade regrouping pattern PR score of the Video Head Impulse Test (vHIT) and its relationship with the slow-phase velocity (SPV) of skull vibration-induced nystagmu
Autor:
Ma Piedad García Díaz, Armin De Luca Sologaistoa, Carlos De Paula Vernetta, M Andres Moreno, Laura Andrea Galeano Paniagua, Manuel Mateos Fernández, Miguel Armengot Carceller
Publikováno v:
International journal of pediatric otorhinolaryngology. 155
Langerhans cell histiocytosis (LCH) is a rare disease of unknown etiology with a heterogeneous and unspecific clinical presentation. Any organ or system may be involved but the most frequent is the skeleton. The diagnostic gold standard is done throu
Autor:
Laura Cavallé-Garrido, Elena Aller, Alba Berzal-Serrano, Rebeca Villanova-Aparisi, Piedad García-Díaz, Miguel Armengot-Carceller, Sara Juárez-Rodríguez, Gema García-García, José M. Millán, Teresa Jaijo, Carlos de Paula-Vernetta
Publikováno v:
Genes, Vol 11, Iss 1467, p 1467 (2020)
Genes
Volume 11
Issue 12
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Genes
Volume 11
Issue 12
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
A cohort of 128 patients from 118 families diagnosed with non-syndromic or syndromic hearing loss (HL) underwent an exhaustive clinical evaluation. Molecular analysis was performed using targeted next-generation sequencing (NGS) with a custom panel t