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  • Review article: Structural ... Review article: Structural brain alterations in prelingually deaf
    Hribar, Manja; Šuput, Dušan; Battelino, Saba ... NeuroImage (Orlando, Fla.), 10/2020, Volume: 220
    Journal Article
    Peer reviewed
    Open access

    Functional studies show that our brain has a remarkable ability to reorganize itself in the absence of one or more sensory modalities. In this review, we gathered all the available articles ...
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  • Glucagon-like peptide-1, a ... Glucagon-like peptide-1, a matter of taste?
    Jensterle, Mojca; DeVries, J. Hans; Battelino, Tadej ... Reviews in endocrine & metabolic disorders, 12/2021, Volume: 22, Issue: 4
    Journal Article
    Peer reviewed

    Understanding of gustatory coding helps to predict, and perhaps even modulate the ingestive decision circuitry, especially when eating behaviour becomes dysfunctional. Preclinical research ...
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  • The importance of flaps in ... The importance of flaps in reconstruction of locoregionally advanced lateral skull-base cancer defects: a tertiary otorhinolaryngology referral centre experience
    Vozel, Domen; Pukl, Peter; Groselj, Ales ... Radiology and oncology, 08/2021, Volume: 55, Issue: 3
    Journal Article
    Peer reviewed
    Open access

    The aim of the study was to identify the value of extensive resection and reconstruction with flaps in the treatment of locoregionally advanced lateral skull-base cancer. The retrospective case ...
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  • Does intervention with GLP-... Does intervention with GLP-1 receptor agonist semaglutide modulate perception of sweet taste in women with obesity: study protocol of a randomized, single-blinded, placebo-controlled clinical trial
    Jensterle, Mojca; Ferjan, Simona; Battelino, Tadej ... Trials, 07/2021, Volume: 22, Issue: 1
    Journal Article
    Peer reviewed
    Open access

    Abstract Background Preclinical studies demonstrated that glucagon-like peptide 1 (GLP-1) is locally synthesized in taste bud cells and that GLP-1 receptor exists on the gustatory nerves in close ...
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  • An innovative strategy for ... An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
    Bonnet, Crystel; Riahi, Zied; Chantot-Bastaraud, Sandra ... European journal of human genetics : EJHG, 12/2016, Volume: 24, Issue: 12
    Journal Article
    Peer reviewed
    Open access

    Usher syndrome (USH), the most prevalent cause of hereditary deafness-blindness, is an autosomal recessive and genetically heterogeneous disorder. Three clinical subtypes (USH1-3) are distinguishable ...
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  • Appropriate Vestibular Stim... Appropriate Vestibular Stimulation in Children and Adolescents-A Prerequisite for Normal Cognitive, Motor Development and Bodily Homeostasis-A Review
    Božanić Urbančič, Nina; Battelino, Saba; Vozel, Domen Children (Basel), 01/2024, Volume: 11, Issue: 1
    Journal Article
    Peer reviewed
    Open access

    The structural development of the vestibular part of the inner ear is completed by birth but its central connections continue to develop until adolescence. Their development is dependent on ...
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  • Autologous Platelet and Ext... Autologous Platelet and Extracellular Vesicle-Rich Plasma as Therapeutic Fluid: A Review
    Troha, Kaja; Vozel, Domen; Arko, Matevž ... International journal of molecular sciences, 02/2023, Volume: 24, Issue: 4
    Journal Article
    Peer reviewed
    Open access

    The preparation of autologous platelet and extracellular vesicle-rich plasma (PVRP) has been explored in many medical fields with the aim to benefit from its healing potential. In parallel, efforts ...
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  • Reliability of parental ass... Reliability of parental assessment of auditory skills in young children: a cross-sectional study in Italian language
    Orzan, Eva; Battelino, Saba; Ciciriello, Elena ... BMJ open, 06/2021, Volume: 11, Issue: 6
    Journal Article
    Peer reviewed
    Open access

    ObjectiveHearing impairments (HIs) that progress or have later onset may have specific effects on language and cognitive development, but are difficult to suspect during routine primary care visits. ...
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