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Št. zadetkov: 5
​Posledice operativnega zdravljenja otoskleroze na spremembo morfologije in zaznavne funkcije jezika
Nina Božanić Urbančič, Saba Battelino
Doktorska disertacija
Oznake: naglušnost;obrazni živec;brbončice;okušalne papile;otološke operacije;mikroskopija;endoskopija;agevzija;nevrofiziologija;denervacija;atrofija.;
Ozadje: Domnevali smo, da manipulacija živca horde timpani (HT) med operacijo stapesa zaradi otoskleroze negativno vpliva na zaznavanje okusa, dvotočkovno diskriminacijo in morfologijo kapilarnih zank fungiformnih papil (FP) na jeziku. Metode: Po končani operaciji stapesa zaradi otoskleroze je kirur ...
Leto: 2023 Vir: Medicinska fakulteta (UL MF)
Unraveling the etiology of pediatric vertigo and dizziness
Nina Božanić Urbančič, Domen Vozel, Jure Urbančič, Saba Battelino
Izvirni znanstveni članek
Oznake: Lyme neuroborreliosis;adolescent;child;
Background and Objectives: Numerous authors have reported that the commonest type of vertigo in children is migraine-associated vertigo (vestibular migraine and benign paroxysmal vertigo of childhood-BPV). We aimed to provide the possible etiological background of vertigo and dizziness in Slovenian ...
Leto: 2021 Vir: Medicinska fakulteta (UL MF)
Indicators of pediatric peripheral vestibular disorder
Nina Božanić Urbančič, Domen Vozel, Špela Kordiš, Manja Hribar, Jure Urbančič, Saba Battelino
Izvirni znanstveni članek
Oznake: otorinolaringologija;vertigo;slabost;uho;izguba sluha;test vestibularne funkcije;pediatrija;
Objectives: This study aims to present characteristics of pediatric patients with peripheral vertigo and dizziness and their clinical workup results in the tertiary otorhinolaryngology center. We wanted to investigate whether the detailed history could replace the extensive vestibular testing and wh ...
Leto: 2022 Vir: Medicinska fakulteta (UL MF)
ǂThe ǂimportance of early genetic diagnostics of hearing loss in children
Nina Božanić Urbančič, Saba Battelino, Tine Tesovnik, Katarina Trebušak Podkrajšek
Pregledni znanstveni članek
Oznake: hearing loss;children;genetic diagnostics;
Hearing loss is one of the most common sensory deficits. It carries severe medical and social consequences, and therefore, universal newborn hearing screening was introduced at the beginning of this century. Affected patients can have hearing loss as a solitary deficit (non-syndromic hearing loss) o ...
Leto: 2020 Vir: Medicinska fakulteta (UL MF)
Novel GRHL2 gene variant associated with hearing loss
Katarina Trebušak Podkrajšek, Tine Tesovnik, Nina Božanić Urbančič, Saba Battelino
Pregledni znanstveni članek
Oznake: autosomal-dominant hearing loss;next-generation sequencing;GRHL2 gene;
In contrast to the recessive form, hearing loss inherited in a dominant manner is more often post-lingual and typically results in a progressive sensorineural hearing loss with variable severity and late onset. Variants in the GRHL2 gene are an extremely rare cause of dominantly inherited hearing lo ...
Leto: 2021 Vir: Medicinska fakulteta (UL MF)
Št. zadetkov: 5
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