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Na voljo sta dva načina iskanja: enostavno in napredno. Enostavno iskanje lahko zajema niz več besed iz naslova, povzetka, ključnih besed, celotnega besedila in avtorja, zaenkrat pa ne omogoča uporabe operatorjev iskanja. Napredno iskanje omogoča omejevanje števila rezultatov iskanja z vnosom iskalnih pojmov različnih kategorij v iskalna okna in uporabo logičnih operatorjev (IN, ALI ter IN NE). V rezultatih iskanja se izpišejo krajši zapisi podatkov o gradivu, ki vsebujejo različne povezave, ki omogočajo vpogled v podroben opis gradiva (povezava iz naslova) ali sprožijo novo iskanje (po avtorjih ali ključnih besedah).

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611 - 620 / 2000
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611.
Nutritional composition of gluten-free labelled foods in the Slovenian food supply
Živa Lavriša, Maša Hribar, Anita Kušar, Katja Žmitek, Igor Pravst, 2020, izvirni znanstveni članek

Ključne besede: gluten-free foods, nutritional composition, food labelling, food supply
Objavljeno v DiRROS: 12.11.2025; Ogledov: 448; Prenosov: 86
.pdf Celotno besedilo (580,04 KB)
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612.
Regulating children's exposure to food marketing on television : are the restrictions during children's programmes enough?
Živa Lavriša, Hristo Hristov, Bridget Kelly, Igor Pravst, 2020, izvirni znanstveni članek

Objavljeno v DiRROS: 12.11.2025; Ogledov: 192; Prenosov: 88
.pdf Celotno besedilo (385,37 KB)
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613.
Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis
Aleksander Turk, Aleš Maver, Peter Juvan, Jelena Drulović, Sarlota Mesaros, Ivana Novaković, Nada Starčević-Čizmarević, Smiljana Ristić, Ivana Stanković Matić, Borut Peterlin, 2025, izvirni znanstveni članek

Povzetek: Multiple sclerosis (MS) is an immune-mediated neurodegenerative disease affecting the central nervous system with many known genetic risk factors. Although genome-wide association studies (GWAS) have identified common genetic variants with small effects associated with MS, the role of rare variants with large effects in MS aetiology remains underexplored. We hypothesized that rare variants in MS-associated genes from GWAS studies (GWAS-associated genes) are more likely to contribute to familial MS (FMS) risk than to sporadic MS (SMS). Therefore, we aimed to assess the burden of rare, predicted pathogenic (RPP) variants in GWAS-associated genes in FMS and SMS patients compared to controls. Rare genetic variants in 111 GWAS-associated genes were assessed in 87 FMS, 89 SMS and 3866 control cases. We demonstrate that RPP variants were significantly overrepresented in the FMS cohort whereas their frequency was not increased in the SMS cohort compared to controls (p-values 5.27 × 10− 74 and 1.00, respectively). Six genes (ALPK2, ANKRD55, INTS8, IQCB1, JADE2, and MALT1) significantly contributed to the burden of RPP in the FMS group. We conclude that rare variants in genes identified by GWAS might contribute to the genetic predisposition of familial MS patients.
Ključne besede: multiple sclerosis, burden analysis, whole exome sequencing (WES), rare variants, rare pathological changes, candidate genes
Objavljeno v DiRROS: 12.11.2025; Ogledov: 177; Prenosov: 82
.pdf Celotno besedilo (1,24 MB)
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Dimensions of the perceived value for wine from the perspective of Slovenian wine consumers
Sandra Bizjak, Hristo Hristov, Aleš Kuhar, 2020, izvirni znanstveni članek

Objavljeno v DiRROS: 12.11.2025; Ogledov: 134; Prenosov: 73
.pdf Celotno besedilo (483,68 KB)
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616.
Secondary parkinsonism associated with focal brain lesions
Rok Berlot, Anđela Pavlović, Maja Kojović, 2024, pregledni znanstveni članek

Povzetek: Focal imaging abnormalities in patients with parkinsonism suggest secondary etiology and require a distinctive clinical approach to diagnosis and treatment. We review different entities presenting as secondary parkinsonism associated with structural brain lesions, with emphasis on the clinical course and neuroimaging findings. Secondary parkinsonism may be due to vascular causes, hydrocephalus, space-occupying lesions, metabolic causes (including acquired hepatocerebral degeneration, diabetic uremic encephalopathy, basal ganglia calcifications, osmotic demyelination syndrome), hypoxic-ischaemic brain injury, intoxications (including methanol, carbon monoxide, cyanide, carbon disulfide, manganese poisoning and illicit drugs), infections and immune causes. The onset can vary from acute to chronic. Both uni-and bilateral presentations are possible. Rigidity, bradykinesia and gait abnormalities are more common than rest tremor. Coexisting other movement disorders and additional associated neurological signs may point to the underlying diagnosis. Neuroimaging studies are an essential part in the diagnostic work-up of secondary parkinsonism and may point directly to the underlying etiology. We focus primarily on magnetic resonance imaging to illustrate how structural imaging combined with neurological assessment can lead to diagnosis. It is crucial that typical imaging abnormalities are recognized within the relevant clinical context. Many forms of secondary parkinsonism are reversible with elimination of the specific cause, while some may benefit from symptomatic treatment. This heterogeneous group of acquired disorders has also helped shape our knowledge of Parkinson's disease and basal ganglia pathophysiology, while more recent findings in the field garner support for the network perspective on brain function and neurological disorders.
Ključne besede: MRI, diagnosis, lesion, parkinsonism, reversible, secondary
Objavljeno v DiRROS: 12.11.2025; Ogledov: 155; Prenosov: 70
.pdf Celotno besedilo (595,24 KB)
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617.
Upgrading disclosure statements for speakers and authors on nephrology : involvement in direct patient care
Jadranka Buturović-Ponikvar, Giorgina Barbara Piccoli, 2025, drugi znanstveni članki

Ključne besede: patient care, nephrology
Objavljeno v DiRROS: 12.11.2025; Ogledov: 131; Prenosov: 60
.pdf Celotno besedilo (1,14 MB)
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