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Št. zadetkov: 13
Samostojni znanstveni sestavek ali poglavje v monografski publikaciji
Oznake: medvrstniško nasilje;etnična raznovrstnost razreda;opora razreda;moralna nezavzetost;mladostniki;
Etnična raznovrstnost razrednih skupnosti, ki lahko predstavlja pomemben dejavnik medvrstniškega nasilja, v zadnjih letih v Sloveniji in Evropi precej narašča. Namen raziskave je bil na vzorcu 6391 udeležencev (87,6 % pripadnikov slovenske etnične pripadnosti) proučiti vlogo etničnega statusa učenca ...
Leto: 2025 Vir: Filozofska fakulteta (UM FF)
Magistrsko delo
Oznake: kakovost v farmacevtski industriji;regulativa v farmacevtski industriji;evropske smernice;pogodbena proizvodnja;
Proces upravljanja sprememb v farmacevtski industriji pri pogodbenih partnerjih
Leto: 2017 Vir: Fakulteta za farmacijo (UL FFA)
Magistrsko delo
Oznake: magistrska dela;etnična raznovrstnost oddelka;izvajanje medvrstniškega nasilja;viktimizacija;
Vzgojno-izobraževalne institucije v zadnjih letih beležijo velik porast etnične raznovrstnosti oddelčnih skupnosti. Eden izmed glavnih trendov raziskav s področja naraščajoče etnične raznovrstnosti oddelkov je preučevanje le-teh v povezavi z medvrstniškim nasiljem. Namen pričujočega dela je bil razi ...
Leto: 2023 Vir: Filozofska fakulteta (UM FF)
Pregledni znanstveni članek
Oznake: psihološka prožnost;kognitivne strategije čustvene regulacije;podnebna anksioznost;sistematični teoretični pregled;psychological resilence;cognitive emotion regulation strategies;climate anxiety;systematic reviews;
The increasing prevalence of climate anxiety and its associations with mental health disorders have encouraged the scien tific community to explore how individuals may effectively cope with this complex phenomenon. While existing research has primarily centered on behavioral strategies, much less is ...
Leto: 2026 Vir: Filozofska fakulteta (UM FF)
Kratki znanstveni prispevek
Oznake: 3-MGA-I;3-methylglutaconic aciduria type 1;precocious puberty;AUH gene;GnRH agonist;triptorelin;
3-methylglutaconic aciduria type 1 (3-MGA-I) (MIM ID #250950) is an ultra-rare, autosomal recessive organic aciduria, resulting from mutated AUH gene, leading to the deficient 3-methylglutaconyl-CoA hydratase (3-MGH). Only around 40 cases are previously reported, caused by a spectrum of 10 mutations ...
Leto: 2020 Vir: Medicinska fakulteta (UL MF)
Izvirni znanstveni članek
Oznake: insulin resistance;oral glucose tolerance test;OGTT;metabolic complications;screening;children;adolescents;obesity;
Background and aims: Early detection of insulin resistance (IR) and obesity-related complications is crucial for preventing type 2 diabetes. This study aimed to identify dynamic metabolic biomarkers for more precise early detection of IR and metabolic abnormalities. Methods: This cross-sectional coh ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Izvirni znanstveni članek
Oznake: newborn screening;NBS;Southeastern Europe;Central Europe;neonatal screening;expanded NBS program;
Newborn screening (NBS) is a well-established public health program that enables early detection and treatment of rare disorders in newborns, preventing severe complications or death. Despite its recognized importance, the scope and implementation of NBS programs vary across Southeastern (SE) and Ce ...
Leto: 2026 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Izvirni znanstveni članek
Oznake: tandem mass spectrometry;MS/MS;fluorometric method;FM;comparison;phenylalanine;Phe;phenylketonuria;PKU;newborn screening;NBS;false positive;recall rate;
Phenylketonuria (PKU) was the first disease to be identified by the newborn screening (NBS) program. Currently, there are various methods for determining phenylalanine (Phe) values, with tandem mass spectrometry (MS/MS) being the most widely used method worldwide. We aimed to compare the MS/MS metho ...
Leto: 2023 Vir: Medicinska fakulteta (UL MF)
Izvirni znanstveni članek
Oznake: BCAT2;branched-chain amino acids;antihistamine branched-chain amino acid transaminase;hypervalinemia;hyperleucine-isoleucinemia;insulin resistance;white matter abnormalities;
Background: Branched-chain amino acid transaminase 2 (BCAT2) deficiency is an autosomal recessive disorder that impairs branched-chain amino acid (BCAA) catabolism. Its clinical and metabolic features remain poorly understood due to limited reports in the literature. Methods: We report three novel c ...
Leto: 2026 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Izvirni znanstveni članek
Oznake: phenylketonuria;newborn;neonatal;screening;international;survey;laboratory;methods;cut-off;
ewborn screening for Phenylketonuria enables early detection and timely treatment with a phenylalanine-restricted diet to prevent severe neurological impairment. Although effective and in use for 60 years, screening, diagnostic, and treatment practices still vary widely across countries and centers. ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Št. zadetkov: 13
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